WO2019116947A1 - Electronic endoscope system - Google Patents

Electronic endoscope system Download PDF

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Publication number
WO2019116947A1
WO2019116947A1 PCT/JP2018/044409 JP2018044409W WO2019116947A1 WO 2019116947 A1 WO2019116947 A1 WO 2019116947A1 JP 2018044409 W JP2018044409 W JP 2018044409W WO 2019116947 A1 WO2019116947 A1 WO 2019116947A1
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WO
WIPO (PCT)
Prior art keywords
light
image
electronic endoscope
light amount
unit
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Application number
PCT/JP2018/044409
Other languages
French (fr)
Japanese (ja)
Inventor
池谷 浩平
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Hoya株式会社
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Publication date
Application filed by Hoya株式会社 filed Critical Hoya株式会社
Priority to JP2019559560A priority Critical patent/JP7211971B2/en
Publication of WO2019116947A1 publication Critical patent/WO2019116947A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/0655Control therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/12Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements

Definitions

  • the present invention relates to an electronic endoscope system for imaging a living tissue in a body cavity.
  • An electronic endoscope system that uses images and information of living tissue in a body cavity captured by an imaging device for diagnosis and treatment is generally known.
  • diagnosis and treatment using an electronic endoscope system in order to obtain an image emphasizing a special part in living tissue, special light of a specific wavelength band different from white light which is ordinary light illuminates living tissue. It is used as light.
  • special light whose light intensity distribution is set to correspond to the absorptivity of the blood vessel is used.
  • An endoscope system capable of capturing a special image using such special light, that is, special light having a spectral intensity characteristic different from that of white light is known (Patent Document 1).
  • the light source device of the known endoscope system includes a first light source unit that emits light of a first wavelength band, a second light source unit that emits light of a second wavelength band, and first and second light source units. It is comprised from the optical path synthetic
  • each light source unit is driven to emit light in the first mode, the light in each wavelength band is emitted at a first intensity ratio, and is synthesized to be ordinary light and supplied to the endoscope.
  • each light source unit when each light source unit is driven to emit light in the second mode, light in each wavelength band is emitted and synthesized at a second intensity ratio at which light in the second wavelength band is relatively low. As a result, it is supplied to the endoscope as special light with high absorbance for a specific living tissue.
  • the wavelength of the special light when illuminating living tissue with special light for diagnosis and treatment, the wavelength of the special light has a high absorptivity of blood in the blood vessel in order to emphasize the image of the blood vessel in living tissue
  • special light in which the peak of the light intensity is matched to the wavelength band corresponding to the wavelength band is set.
  • the light intensity is strong in a narrow wavelength band compared to special light obtained by transmitting only a part of the wavelength band of white light emitted by a conventional halogen lamp or the like. can do.
  • a special light can be used to display a captured image in which an image of blood having a high absorptivity is emphasized more than in the past.
  • Such display of a captured image is used not only for diagnosis of a living tissue but also for treatment of living tissue.
  • special light may be used to search for concentrated lesions in blood vessels of a living tissue, such as a tumor, and perform a treatment to remove the tumor.
  • excising the tumorous part insert the excision treatment tool from the operation part of the endoscope system and project it from the tip surface provided with the illumination window from which the illumination light is emitted and the observation window that receives the light of the image of the imaging subject. While looking at the image taken by the endoscope system, the tumor part is scratched and marked, and then the tumor part is excised using a resection treatment tool.
  • a part of the special light has a light intensity distribution set according to the wavelength band where the absorptivity of blood is high
  • the blood adhering to the illumination window may absorb the part of the light to become heat and warm up, and may be dried on the surface of the illumination window and fixed as a film.
  • the blood adhering to the illumination window needs to be washed before it is fixed.
  • the substance that adheres to the surface of the illumination window is not limited to blood that has flowed into the body cavity, but is a biological substance that is secreted from living tissue, or a body cavity such as a residue of an external substance introduced from outside the body into the body cavity and remaining in the body cavity. There is also an inner substance.
  • the electronic endoscope system is A light source configured to emit illumination light;
  • An imaging device provided in the electronic endoscope and configured to image the living tissue illuminated by the illumination light; It is provided in the processor, and it is determined whether a captured image of the living tissue captured by the imaging device satisfies a determination condition using a ratio of values of different image color components in pixels of the captured image.
  • the light source unit is controlled to change a light amount per unit time of a light component of a part of the light components included in the illumination light according to a determination unit configured to perform and a result of the determination.
  • the determination is a determination as to whether the captured image captured by the imaging element is a captured image including an image of a body cavity material different from the living tissue in the body cavity based on the ratio.
  • the ratio used for the determination condition is the image color component of interest with respect to the value of the image color component of interest of the captured image including the wavelength at which the light reflectance of the body cavity material is highest in the sensitivity wavelength band of the imaging element. It is a ratio of values of image color components other than
  • the light amount changing unit is configured to change the light amount of the light component, with the light component of the illumination light determined according to the absorptivity of the substance in the body cavity as a light amount control target light.
  • the illumination light is combined light obtained by combining a plurality of lights as the light component
  • the light amount changing unit is configured to reduce the light amount of the first light component by dividing it into a first light component for reducing the light amount among the illumination light as the light amount control target light and a second light component for which the light amount is not reduced.
  • the absorptivity of the body cavity substance that absorbs the first light component is larger than the absorptivity of the body cavity substance that absorbs the second light component.
  • the wavelength of the light quantity control target light includes a wavelength at which the absorptivity of the substance in the body cavity is maximum.
  • the determination condition includes a condition whether or not the number of pixels whose ratio is smaller than a predetermined threshold value is larger than a predetermined number as an allowable limit value in the captured image.
  • the imaging device is configured to image the biological tissue in time series; It is preferable that the determination condition includes a condition whether or not the number of pixels of which the temporal change of the ratio has become larger than a predetermined range in the captured image is larger than a predetermined number as an allowable limit value. .
  • the imaging device is configured to image the biological tissue in time series;
  • the determination condition is whether or not the duration in which the number of pixels whose ratio is smaller than a predetermined threshold value is larger than a predetermined number is longer than the predetermined time as the allowable limit value in the captured image. Is preferred.
  • the imaging device is configured to image the biological tissue in time series;
  • the determination condition is that, in the captured image, the duration time in which the number of pixels whose temporal change of the ratio is increased beyond a predetermined range is larger than a predetermined number continues as an allowable limit value. It is preferable that the condition be long or not.
  • the light quantity changer divides the light quantity of the light quantity control target light into a plurality of light quantity levels and sequentially changes them in stages.
  • the determination unit includes a reference table in which the light amount is associated with the allowable limit value in order to change the allowable limit value used in the determination condition according to the light amount after the change of the light amount control target light. Is preferred.
  • the light amount changing unit is configured to control the light source unit to reduce a relative ratio of the light amount of the light amount control target light to the total light amount of the illumination light. Is preferred.
  • the control unit is configured to automatically control the light source unit such that the amount of light of the entire illumination light emitted by the light source unit is increased according to a decrease in an average value of luminance components of the captured image. It has a light quantity adjustment unit, The determination unit is further configured to determine whether or not the light amount of the entire illumination light increased by the automatic light amount adjustment unit exceeds a predetermined amount.
  • the light amount change unit controls the light source unit to change the light amount of the light amount control target light when the determination condition is satisfied and the light amount of the entire illumination light exceeds a predetermined amount.
  • it is configured in
  • the electronic endoscope includes an illumination window for illuminating the illumination light toward the living tissue, an observation window for capturing an image of the living tissue, and a surface of the illumination window and the observation window. Having a tip surface with a fluid discharge port configured to discharge fluid;
  • the electronic endoscope is connected with a fluid delivery mechanism configured to supply the fluid to eject the fluid from the fluid ejection port;
  • the control unit includes a fluid operation control unit configured to control the operation of the fluid delivery mechanism so as to discharge the fluid from the fluid discharge port;
  • the fluid operation control unit controls the operation of causing the fluid to be discharged from the fluid discharge port before the determination unit determines whether the increased total amount of illumination light has exceeded a predetermined amount. Preferably, it is configured to do.
  • the electronic endoscope includes an illumination window for illuminating the illumination light toward the living tissue, an observation window for capturing an image of the living tissue, and a surface of the illumination window and the observation window. Having a tip surface with a fluid discharge port configured to discharge fluid;
  • the electronic endoscope is connected with a fluid delivery mechanism configured to supply the fluid to eject the fluid from the fluid ejection port;
  • the control unit is configured to control the operation of the fluid delivery mechanism so as to discharge the fluid from the fluid discharge port when the light amount changing unit changes the light amount of the light amount control target light
  • an operation control unit is provided.
  • the illumination window is provided at each of two places sandwiching the observation window,
  • the fluid discharge port is provided with a discharge nozzle configured to discharge fluid to each of the illumination window and the observation window.
  • control unit is configured to change the light amount per unit time of the light amount control target light by changing the light intensity of the light amount control target light.
  • the processor includes an image processing unit configured to perform image processing on the captured image;
  • the image processing unit is configured to adjust a gain adjustment amount for an image color component of a wavelength band including the wavelength band of the light amount control target light in the captured image captured by the imaging device after changing the light amount of the light amount control target light. It is preferable that it is configured to change according to the amount of change of the light quantity of the light quantity control target light.
  • the image color component A which is one of the image color components of the captured image, is a wavelength of at least one other light in addition to the wavelength band of the light quantity control target light among the plurality of lights emitted from the light source unit A band is included as a wavelength band of the image color component A,
  • the light quantity changing unit is configured to change the light quantity per unit time of the other light in order to suppress a change in the value of the image color component A when the light quantity of the light quantity control target light is changed. Is preferred.
  • the electronic endoscope system includes a monitor connected to the processor and configured to display the captured image.
  • the control unit determines that the image color component of the captured image satisfies the determination condition.
  • the monitor is configured to transmit the information to notify information indicating that the intracavitary substance may be attached to an illumination window for illuminating the illumination light toward the living tissue. It is preferable that the information control unit be provided.
  • the light amount change unit is configured to change the light amount of the light amount control target light after a predetermined time has elapsed from the information notification by the notification control unit.
  • the substance in the body cavity adheres to the illumination window of the distal end surface of the endoscope and the captured image disappears and diagnosis or It can control that treatment becomes difficult.
  • FIG. 1 is an external perspective view of an electronic endoscope system according to an embodiment. It is a block diagram showing composition of an electronic endoscope system which is one embodiment. It is a figure which illustrates typically the structure of the light source part of the endoscope system shown in FIG. It is a figure which shows an example of the front end surface of the front-end
  • FIG. 1 is an external perspective view of an electronic endoscope system 1 according to an embodiment
  • FIG. 2 is a block diagram showing the configuration of the electronic endoscope system 1.
  • the electronic endoscope system 1 shown in FIG. 1 is a system specialized for medical use, and mainly includes an electronic endoscope (hereinafter referred to as an electronic scope) 100, a processor 200, a light source device 300, and a monitor 400.
  • the electronic scope 100, the light source device 300, and the monitor 400 are connected to the processor 200, respectively.
  • the light source device 300 and the processor 200 are separately provided, the light source device 300 may be integrally provided in the processor 200.
  • the processor 200 includes a system controller 21 and a timing controller 22 as shown in FIG.
  • the system controller 21 is a control unit that executes various programs stored in a memory (not shown) and integrally controls the entire electronic endoscope system 1, and is configured by software or hardware. Further, the system controller 21 is connected to the operation panel 24.
  • the system controller 21 changes each operation of the electronic endoscope system 1 and parameters for each operation according to an instruction from the operator input to the operation panel 24.
  • the input instruction by the operator includes, for example, an instruction to switch the observation mode of the electronic endoscope system 1.
  • the observation modes include a normal observation mode in which white light is observed as illumination light and a special observation mode in which special light is observed as illumination light.
  • the timing controller 22 outputs clock pulses for adjusting the timing of operation of each unit to each circuit in the electronic endoscope system 1.
  • the light source device 300 includes a light source unit 310 and a condenser lens 350, as shown in FIG.
  • FIG. 3 is a diagram schematically illustrating the configuration of the light source unit 310.
  • the light source unit 310 includes four light source units 312 to 315, three optical elements 333 to 335, collimating lenses 322 to 325, and a light source driving circuit 340.
  • the light source drive circuit 340 generates a drive current for driving the light source units 312 to 315 with the controlled light intensity in accordance with the control signal of the system controller 21 and sends it to each light source unit.
  • the light source units 312 to 315 include light emitting diodes (LEDs: Light Emitting Diodes) that emit light of a wavelength band of a predetermined color.
  • the collimator lenses 322 to 325 are disposed on the light path of the emitted light on the front surface of each of the light source units 312 to 315, and convert the emitted light into parallel light.
  • the optical elements 333 to 335 have a function of transmitting or reflecting incident light.
  • the optical elements 332 to 335 use, for example, a dichroic mirror or a dichroic prism.
  • the optical elements 333 to 335 reflect the light component of the wavelength band set as the wavelength characteristic in each of the optical elements 333 to 335 among the incident light, and transmit the light components of the remaining wavelength bands.
  • the optical elements 333 to 335 have wavelength characteristics set according to the wavelength bands of the light emitted from the light source units 312 to 315, so that the light of the wavelength band set by the optical elements 333 to 335 is multiplexed. It becomes one illumination light.
  • the light source unit 312 is, for example, a red LED that emits light in a red wavelength band (for example, a wavelength of 620 to 680 nm), and the light source unit 313 is light in a blue wavelength band (for example, a wavelength of 430 to 470 nm) And a green phosphor 313b.
  • the green phosphor 313b is excited by the blue LED light emitted from the blue LED 313a, and emits fluorescence in a green wavelength band (for example, a wavelength of 470 to 600 nm).
  • the light source unit 314 includes a blue LED that emits light in a blue wavelength band (for example, a wavelength of 430 to 470 nm).
  • the light source unit 315 includes a purple LED that emits light in a purple wavelength band (eg, a wavelength of 395 to 435 nm). The purple wavelength band at least includes the wavelength 415 nm.
  • the transmitted light and the reflected light are combined at each position of the optical elements 333 to 335 having wavelength characteristics set according to such a wavelength band of light. Therefore, in the light source unit 310, the light emitted from the plurality of light source units is combined with the light having a desired wavelength band and emitted from the light source unit 310 as illumination light.
  • the light source drive circuit 340 changes the light intensity of the light emitted from the light source units 312 to 315 in the case where the white light used in the normal observation mode is the illumination light and the special light used in the special observation mode is the illumination light. Configured to Although the light source unit 310 has a configuration in which the optical elements 333 to 335 are arranged in series as shown in FIG. 3, the present invention is not limited to this configuration.
  • illumination light is synthetic light which compounded a plurality of lights as a light component.
  • the illumination light L emitted from the light source unit 310 is condensed by the condenser lens 350 on the incident end face of a light carrying bundle (LCB) 11 described later, which is formed of a bundle of plural optical fibers. And enter the LCB 11.
  • LCB light carrying bundle
  • the electronic scope 100 mainly includes a connection portion 50, an operation portion 52, an insertion portion 54, and a cable 51 connecting the connection portion 50 and the operation portion 52.
  • the insertion portion 54 includes a flexible tube 58 connecting the operation portion 52 and the distal end portion 56 of the insertion portion 50.
  • an LCB 11 Inside the flexible tube 58, an LCB 11, an air / water tube for sending a fluid such as water or air, a treatment instrument introduction tube, a signal line and the like are provided inside the flexible tube 58.
  • the treatment instrument introduction tube is a tube for inserting a treatment instrument for treating (for example, cutting and removing) living tissue from the operation unit 52 and projecting it from the tip portion 56 to treat the living tissue. .
  • the signal line includes a transmission line for transmitting a captured image signal from a solid-state imaging device 14 described later and a control line for transmitting a control signal from the processor 200 to the solid-state imaging device 14.
  • the distal end portion of the operation unit 52 of the electronic scope 100 is a flexible insertion portion 54 for insertion into the human body. In the vicinity of the distal end of the insertion portion 54, a bending portion 60 connected to the proximal end of the insertion portion 54 is provided, and the bending portion 60 bends in response to the remote control in the operation portion 52.
  • the bending mechanism of the bending portion 60 is a known mechanism incorporated in a general endoscope.
  • the bending structure is to bend the bending portion 60 by pulling the operation wire interlocked with the rotation operation of the bending operation knob provided in the operation portion 52.
  • a tip portion 56 provided with a solid-state imaging device 14 is provided.
  • the distal end portion 56 of the electronic scope 100 has an illumination light emitting end of the LCB 11 disposed over substantially the entire length from the connection portion 50 to the distal end portion 56.
  • the light distribution lens is provided in front of the illumination light emission end of the LCB 11 at the distal end portion 56, and the front surface on the living tissue side of the light distribution lens is the illumination window 12 for emitting illumination light.
  • the distal end portion 56 is provided with an objective lens for forming an image of a living tissue, and the front surface on the living tissue side of the objective lens is an observation window 13 for receiving light of the image of the living tissue.
  • the tip end portion 56 is provided with a solid-state imaging device 14 for receiving the formed image, and an amplifier (not shown) for amplifying an image signal output from the solid-state imaging device 14.
  • the illumination light that has entered the LCB 11 propagates in the LCB 11, exits from the illumination light output end of the LCB 11, and illuminates the subject of the biological tissue as illumination light through the illumination window 12 configured with a light distribution lens.
  • the return light from the subject of the illumination light emitted from the illumination window 12 forms an optical image on the light receiving surface of the solid-state imaging device 14 through the observation window 13 constituted by the objective lens.
  • the light source unit 310 of the light source device 300 may be embedded in the tip end portion 56 of the electronic scope 100 when the configuration is compact. In this case, the LCB 11 and the condenser lens 350 for guiding the illumination light from the light source unit 310 to the distal end portion 56 are unnecessary.
  • FIG. 4 is a view showing an example of the distal end surface 57 of the distal end portion 56.
  • two illumination windows 12 composed of light distribution lenses provided in front of the tip of the LCB 11 are provided, and further, they are composed of objective lenses so as to be sandwiched between the illumination windows 12
  • An observation window 13 is provided.
  • the air / water supply port 64 is a portion that receives the supply of fluid from the fluid delivery mechanism (see FIG.
  • the air / water supply port 64 has three discharge nozzles, and the discharge nozzles are configured to spray and wash water and air on each of the two illumination windows 12 and one observation window 13. It is done. Further, instead of the end face 57 shown in FIG. 4, the air / water supply port 64 may be provided separately from the air supply port for discharging air and the water supply port for discharging water.
  • the solid-state imaging device 14 is a single-plate color imaging device having a Bayer-type pixel arrangement.
  • the solid-state imaging device 14 accumulates an optical image formed by each pixel on the light receiving surface as an electric charge according to the light quantity, and generates image signals of R (Red), G (Green), and B (Blue). Output.
  • the solid-state imaging device 14 is a charge coupled device (CCD) image sensor or a complementary metal oxide semiconductor (CMOS) image sensor. Alternatively, an imaging device other than the image sensor may be used.
  • a color filter that defines a wavelength band in an image color component of a captured image of the solid-state imaging device 14 is provided in front of each light receiving position of the solid-state imaging device 14.
  • the solid-state imaging device 14 repeatedly images the living tissue at timing according to the clock pulse transmitted from the timing controller 22. That is, the solid-state imaging device 14 is configured to image a living tissue in time series. In other words, the solid-state imaging device 14 is configured to obtain a moving image of a living tissue.
  • a driver signal processing circuit 15 and a memory 16 are provided as shown in FIG.
  • the driver signal processing circuit 15 receives an image signal of a living tissue from the solid-state imaging device 14 in a frame cycle.
  • the frame period is, for example, 1/30 seconds.
  • the driver signal processing circuit 15 performs predetermined processing on the image signal input from the solid-state imaging device 14, and outputs the processed signal to the pre-stage signal processing circuit 26 of the processor 200.
  • the driver signal processing circuit 15 also accesses the memory 16 to read out the unique information of the electronic scope 100.
  • the unique information of the electronic scope 100 recorded in the memory 16 includes, for example, the number of pixels and sensitivity of the solid-state imaging device 14, an operable frame rate, and a model number.
  • the driver signal processing circuit 15 outputs the unique information read from the memory 16 to the system controller 21.
  • the system controller 21 performs various operations based on the unique information of the electronic scope 100 to generate a control signal.
  • the system controller 21 controls the operation and timing of various circuits in the processor 200 so that processing suitable for the electronic scope 100 connected to the processor 200 is performed using the generated control signal.
  • the timing controller 22 supplies clock pulses to the driver signal processing circuit 15 according to the timing control by the system controller 21.
  • the driver signal processing circuit 15 drives and controls the solid-state imaging device 14 at timing synchronized with the frame rate of the image processed on the processor 200 side according to the clock pulse supplied from the timing controller 22.
  • the pre-stage signal processing circuit 26 performs predetermined image processing such as demosaicing, matrix calculation, gain adjustment, and color balance processing on the image signal of the captured image input from the driver signal processing circuit 15 in one frame cycle, It is output to the image memory 27.
  • predetermined image processing such as demosaicing, matrix calculation, gain adjustment, and color balance processing
  • the image memory 27 buffers an image signal input from the front stage signal processing circuit 26, and outputs the image signal to the rear stage signal processing circuit 28 in accordance with timing control by the timing controller 22.
  • the post-stage signal processing circuit 28 processes the image signal input from the image memory 27 to generate screen data for monitor display, and converts the generated screen data for monitor display into a predetermined video format signal.
  • the converted video format signal is output to the monitor 400.
  • the moving image of the biological tissue taken in time series by the electronic scope 100 is displayed on the display screen of the monitor 400.
  • the electronic endoscope system 1 has a plurality of observation modes including a normal observation mode and a special observation mode for observing a living tissue.
  • Each observation mode is switched manually or automatically according to the living tissue to be observed. For example, when it is desired to illuminate and observe a living tissue with white light, the observation mode is switched to the normal observation mode by, for example, an input instruction through the operation panel 24.
  • white light includes pseudo white light in which light of a plurality of wavelength bands is mixed, not having a flat spectral intensity distribution.
  • the observation mode is switched to the special observation mode by, for example, an input instruction through the operation panel 24.
  • FIG. 5 is a diagram showing an example of a spectral waveform of special light used in the special observation mode.
  • FIG. 6 is a diagram showing an example of a spectral waveform of white light used in the normal observation mode, specifically, pseudo white light.
  • purple light Lv having a wavelength band of 395 to 435 nm
  • blue light Lb having a wavelength band of 430 to 470 nm
  • green light Lg having a wavelength band of 470 to 600 nm
  • illumination light obtained by combining red light Lr having a wavelength band of 620 to 680 nm.
  • the light intensity of the purple light Lv is overwhelmingly stronger than the light intensities of the other lights.
  • the light intensity of each light is adjusted.
  • Such special light or pseudo white light can be changed by adjusting the amount of light emitted from the light source units 312 to 315 per unit time.
  • the adjustment of the light amount per unit time is performed, for example, by adjusting the light intensity, or by adjusting the irradiation time when the illumination light is pulse lighting.
  • a body cavity material may adhere to the illumination window 12 and be fixed.
  • blood is described as a representative example of a substance in a body cavity.
  • special observation using special light as illumination light
  • the mode is used.
  • special light that can distinguish between a normal part and a lesion part (tumor part) of a living tissue is used as illumination light.
  • the living tissue is treated, for example, by excision, blood easily flows into the body cavity and adheres to the distal end surface 57 of the distal end portion 56.
  • the blood adhering to the observation window 13 of the distal end surface 57 is reflected on the captured image, so it is possible to judge the presence or absence of the blood adhesion.
  • the fluid such as water or air from the air / water supply port 64 immediately to wash the surface and remove the blood.
  • the blood adheres to the illumination window 12 it is difficult to confirm the adhesion of the blood, so the blood may be left until it coagulates and adheres on the surface of the illumination window 12.
  • the special light used in the special observation mode often makes the light intensity of the purple light Lv having the wavelength band where the light absorption of blood is the highest the light intensity of the purple light Lv in the pseudo white light,
  • the blood adhering to the illumination window 12 absorbs purple light Lv and tends to coagulate earlier than the blood adhering to the observation window 13. For this reason, when the possibility of adhering to the illumination window 12 is high, it is preferable to determine early that the possibility that blood has adhered to the illumination window 12 and to wash the surface of the illumination window 12.
  • the electronic endoscope system 1 has a high possibility that blood may adhere to the illumination window 12 so that blood can be removed early even if blood adheres to the surface of the illumination window 12 It has a configuration that can be determined. That is, when imaging the living tissue in the body cavity while treating the living tissue, the electronic endoscope system 1 adheres and adheres the blood which is the body cavity material to the illumination window 12 of the distal end surface 57, thereby capturing the captured image. It has the composition which controls becoming defective.
  • FIG. 7 is a diagram for explaining the configuration of the system controller 21 of the processor 200.
  • the system controller (control unit) 21 generates a control signal for controlling and managing the operation of each part of the electronic endoscope system 1 and transmits it to each part, in addition to the system operation control unit 21A
  • a determination unit 21B and a light amount change unit 21C are provided.
  • the determination unit 21B is a portion that determines whether or not the image color component of the captured image of the biological tissue repeatedly captured at predetermined time intervals by the solid-state imaging device 14 satisfies the set determination condition.
  • the determination condition is a condition using a ratio of values of different image color components in each pixel of the captured image. Specifically, the determination unit 21B determines the determination condition in order to make the above determination on a captured image including an image of a substance in the body cavity different from the living tissue in the body cavity, for example, a captured image including an image of blood. The determination is performed by calculating the ratio of the values of image color components other than the target image color component to the value of the target image color component of the captured image as the above ratio used for.
  • the target image color component of the captured image is an image color component of the captured image including the wavelength at which the light reflectance of blood (subjacent substance) is the highest in the sensitivity wavelength band of the solid-state imaging device 14.
  • the target image color component of the captured image including the wavelength with the highest light reflectance is the red light component most reflected in the case of blood, so the target image color component is the image of the image captured by the solid-state imaging device 14 It is a red image color component.
  • FIG. 8 is a diagram showing an example of a spectral waveform of the transmittance of the primary color filter provided on the front surface of each light receiving position of the solid-state imaging device 14.
  • the wavelength band where the transmittance is greater than 0 is the sensitivity wavelength band in the solid-state imaging device 14.
  • the determination unit 21B calculates the ratio of the value of the target image color component of the captured image to the value of the other image color components.
  • the target image color component is the red color component R of the wavelength band indicated by R shown in FIG.
  • the ratio calculated by the determination unit 21B is Db / Dr or Dg / Dr.
  • the reason for using the ratio of image color components in the same pixel is to eliminate the influence of the luminance which is different for each pixel. Therefore, instead of Db / Dr or Dg / Dr, it is also possible to use the ratio of the value of Dr to the luminance component in the same pixel. Using such a ratio, the determination unit 21B determines whether the image color component of the captured image satisfies the determination condition.
  • the determination condition is, for example, when there are a large number of pixels for which the value of Db / Dr or Dg / Dr is equal to or less than the threshold in the captured image, that is, when there are many images of blood in the captured image It is a condition for determining that blood is likely to have flowed out and the blood has adhered to the illumination window 12. Such determination conditions will be described later.
  • the light amount changing unit 21C changes the light amount per unit time of some of the plurality of lights emitted by the light source device 300 according to the determination result of the determining unit 21B, for example, a light source to reduce the light amount.
  • the device 300 is controlled. In one embodiment, reducing the light intensity reduces the amount of light per unit time. In another embodiment, when the light intensity is reduced, the period during which the solid-state imaging device 14 performs imaging by photoelectric conversion is removed while the light intensity is kept constant, or the light emission is continuously performed for a certain period or By switching off intermittently, the amount of light per unit time is changed (decreased).
  • the light quantity changing unit 21C changes the light quantity by using the light component of the illumination light determined according to the absorptivity of the substance in the body cavity as the light quantity control target light so that the light absorption of the substance in the body cavity is reduced. More specifically, the light quantity change unit 21C sets the light quantity control target as the light quantity control target light whose light absorptivity of blood is higher than a predetermined value, for example, the highest light among the lights emitted by the light source device 300. The operation of the light source drive circuit 340 is controlled to change the amount of light.
  • FIG. 9 is a diagram showing a spectral waveform of blood absorptivity. As shown in FIG.
  • the absorptivity of blood is maximized in the range of 410 to 420 nm, particularly at 415 nm. For this reason, the light amount control target light whose light intensity is reduced becomes purple light Lv emitted from the light source unit 315.
  • the light amount changing unit 21C converts the light component of the illumination light determined according to the absorptivity of the body cavity substance so that the light absorption of the body cavity substance is reduced.
  • the light quantity is changed as the control target light.
  • the light amount changing unit 21C divides the illumination light L into a first light component for reducing the light amount and a second light component not for reducing the light amount as the light amount control target light. It is configured to reduce the amount of light of one light component.
  • the absorptivity of the body cavity material that absorbs the first light component is larger than the absorptivity of the body cavity material that absorbs the second light component.
  • the light quantity control target light is, for example, a light component in which the absorptivity of the substance in the body cavity is higher than a predetermined value, and more preferably a light component having the maximum absorptivity. is there.
  • the wavelength of light subject to light quantity control includes a wavelength at which the absorptivity of the substance in the body cavity is maximum.
  • the light intensity of the light quantity control target light does not have to be reduced to the level of the light intensity of the purple light Lv in the pseudo white light as indicated by the dotted line in FIG. 5, for example. It may be reduced to the light intensity of the purple light Lv at.
  • the light amount changing unit 21C may reduce the relative ratio of the light amount of the light amount control target light to the light amount of the entire illumination light, instead of reducing the light intensity.
  • the determination unit 21B determines that the possibility of blood adhering to the illumination window 12 is high, according to one embodiment, in the captured image, the above-mentioned ratio Db / Dr or Dg / Dr is a predetermined threshold value. It is preferable to include the condition A whether or not the smaller number of pixels is larger than a predetermined number as the allowable limit value. In the captured image, when the ratio is smaller than a predetermined threshold, for example, when the number of pixels of the image of blood is large, it can be said that blood is likely to be attached to the illumination window 12.
  • the upper limit of the predetermined allowable occupancy rate of the number of pixels of the image of blood occupied in all pixels of the captured image, and the number of all pixels of the captured image The pixel in the specific area (for example, a rectangular or circular area smaller than the image size of the captured image and including the central position of the captured image) in the captured image may be used. .Times..times..times..times..times..times..times...times...times...times...times...times...times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..times..
  • the determination condition is predetermined as the allowable limit value of the number of pixels of which the temporal change of the above-mentioned ratio increases beyond a predetermined range. It is preferable to include the condition B which is larger than the number.
  • the temporal change of the ratio is, for example, the ratio of the above-mentioned ratio in two captured images adjacent to each other among the captured images of moving images obtained in time series divided by the difference between the captured times of the two captured images. is there.
  • the time change of the above ratio (when the time change is negative, it means the absolute value of the time change) becomes larger than the predetermined range (the change of the ratio is large Therefore, when such a number of pixels is large, it means that blood has flowed out on the living tissue, and it can be said that there is a high possibility that the blood has adhered to the illumination window 12.
  • the upper limit of the predetermined allowable occupancy rate of the number of pixels changing to the image of blood occupied in all the pixels of the captured image as the above-mentioned allowable limit value of the number of pixels changed from the image of living tissue to the image of blood in this way
  • a product obtained by multiplying the number of all pixels of the captured image may be used, or a specific area near the center position in the captured image (for example, smaller than the image size of the captured image, including the center position of the captured image)
  • the number of pixels in the rectangular or circular area may be multiplied by the upper limit of the predetermined allowable occupancy rate of the number of pixels changing to the image of blood occupied in this specific area.
  • the determination conditions include condition A and condition B simultaneously. In this case, when the number of pixels under condition A, condition B, or condition A and condition B is larger than a predetermined number, the light quantity changing unit 21C controls the light source device 300 to reduce the light quantity of light subject to light quantity control. Is also preferred.
  • the determination condition is that, in the captured image obtained in time series, the duration for which the number of pixels whose ratio is smaller than the predetermined threshold is larger than the predetermined number continues to be permitted. It is preferable to include the condition C as to whether the value is longer than a predetermined time.
  • the number of pixels whose ratio is smaller than a predetermined threshold value is continuously present for a predetermined time, for example, when the image of blood is continuously present for a predetermined time, blood may be attached to the illumination window 12 It can be said that the sex is high.
  • the determination condition is that, in the captured images obtained in time series, the state in which the number of pixels whose temporal change of the above-mentioned ratio increases beyond a predetermined range is larger than a predetermined number continues It is preferable to include the condition D whether the duration is longer than a predetermined time as an allowable limit value.
  • the number of pixels in which the temporal change of the ratio is increased beyond a predetermined range for example, the number of pixels which has been rapidly changed from an image of a living tissue to an image of blood continuously exists for a predetermined time. Is rapidly increasing and continuously existing for a predetermined time, it is highly likely that blood has flowed into the body cavity and blood has adhered to the illumination window 12.
  • the determination unit 21B may make a determination using a combination of at least two of the above conditions A to D as the determination condition. According to one embodiment, when the conditions A and B are satisfied and the conditions C and D are satisfied, the light quantity control unit 21B may control the light source device 300 to reduce the light quantity of the light quantity control target light. preferable.
  • the light quantity changing unit 21B may divide the light quantity per unit time of the light quantity control target light into a plurality of light quantity levels and sequentially change the light quantity in a stepwise manner.
  • the determination unit 21B determines the light intensity (light amount) after the change of the light amount control target light. It is preferable to provide a reference table for changing the allowable limit values of the above-mentioned conditions A to D, that is, the predetermined number or the above-mentioned predetermined time, which is used in the judgment condition.
  • the reference table is information in which the light intensity of the light amount control target light and the above-described allowable limit value used in the determination condition are stored in association with each other.
  • the above predetermined number used as the allowable limit value or the above predetermined time is the light quantity control target Different from the tolerance limits used when the light intensity level is low. It is preferable to change the allowable limit value according to the intensity level of the light quantity control target light in order to make the determination with high accuracy.
  • FIG. 10 is a diagram illustrating an example of the configuration of the system controller 21 according to an embodiment.
  • the operation unit 52 of the electronic scope 100 is a fluid delivery mechanism 70 (for example, a syringe pump or the like) that supplies air or water to discharge air or water (fluid) from the air / water supply port 64. Connected with The fluid delivery mechanism is connected to the operation unit 52 through a pipe for supplying air or water.
  • the system controller 21 preferably includes a fluid operation control unit 21D that controls the operation of the fluid delivery mechanism.
  • the fluid operation control unit 21D perform the control of the operation of the fluid delivery mechanism 70 from the point of removing blood adhering early.
  • FIG. 11 is a diagram showing an example of the configuration of a system controller 21 according to still another embodiment.
  • the system controller (control unit) 21 determines the light source device according to the decrease in the average value of the luminance components of the captured image.
  • the automatic light amount adjustment unit 21E may be provided to control the light source drive circuit 340 of the light source device 300 such that the light amount of the entire illumination light emitted by the light source 300 increases (so that the light amount increases uniformly in the entire wavelength band).
  • the automatic light quantity adjustment unit 21E is generally used to suppress fluctuations in the luminance of a captured image due to the length (short distance) of the distance (imaging distance) between the living tissue as the subject and the distal end surface 57.
  • the automatic light amount adjustment unit 21E can be effectively used also in the determination by the determination unit 21B. That is, in addition to the determination using the determination condition, the determination unit 21B further determines whether the increased light amount of the entire illumination light (light amount per unit time) exceeds a predetermined amount. It is preferable to control the light source device 300 so as to change the light quantity of the light quantity control target light when the light quantity of the entire illumination light exceeds a predetermined quantity.
  • the automatic light amount adjustment unit 21E increases the light amount so that the brightness of the illumination light becomes constant. Do. However, even if the automatic light quantity adjustment unit 21E increases the light quantity of the illumination light, the improvement of the average value of the luminance components of the captured image is not sufficient, and if the average value is still small, the possibility of blood adhering to the illumination window 12 Is high. In this case, the light quantity of the entire illumination light is larger than usual.
  • the automatic light quantity adjustment unit 21E can acquire information on the light quantity of the present illumination light L emitted from the light source device 300 from the control signal that the automatic light quantity adjustment unit 21E sends to the light source drive circuit 340. Furthermore, in another embodiment, the system controller 21 shown in FIG.
  • the fluid operation control unit 21D receives air or water from the air / water supply port 64 ( It is preferable to control the operation of discharging the fluid. Since the illumination window 12 is cleaned before the determination of the light amount of the illumination light in the determination unit 21B, the cleaned illumination window 12 can be used as the determination target.
  • the processor 200 includes a pre-processing circuit 26 (image processing unit) that performs image processing on a captured image.
  • the pre-processing circuit 26 adjusts the gain of the image signal of the captured image.
  • the pre-processing circuit 26 generates an image color component of a wavelength band including the wavelength band of the light amount control target light in the captured image captured by the solid-state imaging device 14 after changing the light amount of the light amount control target light It is preferable to change the gain adjustment amount for the color component in accordance with the change amount of the light quantity of the light quantity control target light.
  • the light quantity control target light is purple light Lv, and this purple light Lv is included in the blue (B) wavelength band as shown in FIG.
  • the amount of change of the light quantity of the purple light Lv According to the amount of change of the light quantity of the purple light Lv. Specifically, when the light amount of the purple light Lv is reduced, the gain for increasing the value of the blue image color component is increased as the light amount of the purple light Lv is decreased. Thereby, even when the light amount of the light to be controlled is reduced, the color balance of the captured image displayed on the monitor 400 is maintained before and after the change of the light amount, and the operator does not stress the captured image of the living tissue. It can be observed.
  • the wavelength band of blue (B) also includes the wavelength band of blue light Lb emitted from the light source unit 314. Therefore, when the light amount of the purple light Lv is decreased, it is also preferable to increase the light amount of the blue light Lb and maintain the color balance of the captured image displayed on the monitor 400 before and after the change of the light amount.
  • an image color component A (for example, a blue image color component) which is one of the image color components of the captured image is a light quantity control target light (for example, violet light) among a plurality of lights emitted from the light source device 300
  • a light quantity control target light for example, violet light
  • the wavelength band of at least one other light for example, blue light Lb
  • the wavelength band of the image color component A is included as the wavelength band of the image color component A.
  • the light quantity changing unit 21C changes (for example, reduces) the light quantity of the light quantity control target light (for example, purple light Lv), the change of the value of the image color component A (blue image color component) In order to suppress, it is preferable to change (increase) the light amount per unit time of another light (for example, blue light Lb).
  • Such an embodiment may be performed in combination with the above-described change in gain adjustment amount.
  • the system controller 21 control unit information that blood may be attached to the illumination window 12 for illuminating the illumination light toward the living tissue.
  • the notification control unit 21F transmits the above information to the monitor 400, as shown in FIG.
  • the operator can manually clean the illumination window 12 at an early stage. For this reason, it can suppress that blood adheres to the illumination window 12.
  • the notification control unit 21F transmit information so that the monitor 400 can notify that the observation in the body cavity in the special observation mode can be continued.
  • the light quantity change unit 21C changes the light quantity of the light quantity control target light It is preferred to do.
  • the operator can prepare for the possibility of color change of the captured image, and can continue stable observation, diagnosis or treatment.
  • the light intensity of the light quantity control target light may be returned to the original light intensity.
  • the body cavity material is described for blood that has flowed into the body cavity, but the body cavity material is a biological material that is secreted from living tissue and is introduced from outside the body into the body cavity and remains in the body cavity. It contains substances in the body cavity such as residues of external substances (food).
  • the light quantity control target light is not limited to purple light and changes according to the absorptivity of the substance in the body cavity.
  • the type of the target image color component of the captured image used for the determination condition also changes according to the reflection characteristic of the substance in the body cavity.
  • the light amount changing unit 21C causes at least one of the illumination light to be reduced according to the absorptivity of the body cavity material so that the light absorption of the body cavity material is reduced according to the result determined by the determining unit 21B.
  • the light component is configured to change the light quantity as the light quantity control target light. Specifically, the light quantity of light having a high absorptivity of the substance in the body cavity is configured to be reduced. However, the light quantity control target light may increase the light quantity of light having a low absorptivity.
  • the electronic endoscope system of the present invention was explained in detail, the electronic endoscope system of the present invention is not limited to the above-mentioned embodiment, In the range which does not deviate from the main point of the present invention, various improvement or change Of course it is good.

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Abstract

This electronic endoscope system includes: a light source unit for emitting illumination light; an imaging element that is provided on an electronic endoscope and is for capturing an image of biological tissue illuminated with the illumination light; and a control unit. The control unit is provided in a processor and includes: a determination unit for determining whether an image color component of the image of the biological tissue repeatedly captured by the imaging element satisfies determination conditions that use a ratio of different image color component values in each pixel of the image; and a light amount changing unit for changing the amount of light as a result of the determination and according to the light absorptivity of a substance within a body cavity, the light for which the amount is subject to control being at least a portion of a light component of the illumination light.

Description

電子内視鏡システムElectronic endoscope system
 本発明は、体腔内の生体組織を撮像する電子内視鏡システムに関する。 The present invention relates to an electronic endoscope system for imaging a living tissue in a body cavity.
 撮像素子で撮影された体腔内の生体組織の画像や情報を診断及び処置のために用いる電子内視鏡システムが一般的に知られている。電子内視鏡システムを用いた診断及び処置では、生体組織中の特殊な部分を強調した画像を得るために、通常光である白色光とは異なる特定の波長帯域の特殊光が生体組織の照明光として用いられる。例えば、生体組織中の血管の部分を強調した像を得るために、光強度分布を血管の吸光率に対応させて設定した特殊光が用いられる。このような特殊光、すなわち、分光強度特性が白色光と異なる特殊光を用いて、特殊な画像を撮影することが可能な内視鏡システムが知られている(特許文献1)。 2. Description of the Related Art An electronic endoscope system that uses images and information of living tissue in a body cavity captured by an imaging device for diagnosis and treatment is generally known. In diagnosis and treatment using an electronic endoscope system, in order to obtain an image emphasizing a special part in living tissue, special light of a specific wavelength band different from white light which is ordinary light illuminates living tissue. It is used as light. For example, in order to obtain an image in which a portion of a blood vessel in a living tissue is emphasized, special light whose light intensity distribution is set to correspond to the absorptivity of the blood vessel is used. An endoscope system capable of capturing a special image using such special light, that is, special light having a spectral intensity characteristic different from that of white light is known (Patent Document 1).
 上記公知の内視鏡システムの光源装置は、第1の波長帯域の光を射出する第1の光源ユニットと、第2の波長帯域の光を射出する第2の光源ユニットと、第1及び第2の光源ユニットから射出される光の光路を合成する光路合成手段と、各光源ユニットを個別に発光制御する光源制御手段と、から構成される。各光源ユニットが第1のモードで発光駆動されると、各波長帯域の光が第1の強度比で射出され、合成されることにより、通常光となって内視鏡に供給される。また、各光源ユニットが第2のモードで発光駆動されると、各波長帯域の光が、第2の波長帯域の光が相対的に低くなる第2の強度比で射出され、合成されることにより、特定の生体組織に対して吸光度の高い特殊光となって内視鏡に供給される。 The light source device of the known endoscope system includes a first light source unit that emits light of a first wavelength band, a second light source unit that emits light of a second wavelength band, and first and second light source units. It is comprised from the optical path synthetic | combination means which synthesize | combines the optical path of the light inject | emitted from 2 light source units, and the light source control means which carries out light emission control of each light source unit separately. When each light source unit is driven to emit light in the first mode, the light in each wavelength band is emitted at a first intensity ratio, and is synthesized to be ordinary light and supplied to the endoscope. Further, when each light source unit is driven to emit light in the second mode, light in each wavelength band is emitted and synthesized at a second intensity ratio at which light in the second wavelength band is relatively low. As a result, it is supplied to the endoscope as special light with high absorbance for a specific living tissue.
国際公開第2017/142097号International Publication No. 2017/142097
 上記内視鏡システムでは、診断及び処置のために生体組織を特殊光で照明するとき、生体組織中の血管の像を強調するために、特殊光の波長は血管中の血液の吸光率が高い波長帯域に対応した波長帯域に光強度のピークを合わせた特殊光を設定することが多い。また、上記光源装置では、発光ダイオードが用いられるため、従来のハロゲンランプ等が出射する白色光の一部の波長帯域のみを透過させて得られる特殊光に比べて狭い波長帯域で光強度を強くすることができる。このため、特殊光を用いて、吸光率の高い血液の像を従来より強く強調した撮像画像を表示することができる。このような撮像画像の表示は、生体組織の診断だけでなく、生体組織の処置時にも用いられる。例えば、特殊光を用いて生体組織の血管の集中した病変部、例えば腫瘍部分を探し出し、この腫瘍部分を切除する処置を行う場合もある。腫瘍部分を切除する場合、内視鏡システムの操作部から切除用処置具を挿入し、照明光が出射する照明窓及び撮像被写体の像の光を受け入れる観察窓を備えた先端面から突出させ、内視鏡システムで撮像した画像を見ながら、腫瘍部分に傷をつけてマーキングした後、切除用処置具を用いて腫瘍部分を切除する。 In the above endoscope system, when illuminating living tissue with special light for diagnosis and treatment, the wavelength of the special light has a high absorptivity of blood in the blood vessel in order to emphasize the image of the blood vessel in living tissue In many cases, special light in which the peak of the light intensity is matched to the wavelength band corresponding to the wavelength band is set. Further, in the above light source device, since a light emitting diode is used, the light intensity is strong in a narrow wavelength band compared to special light obtained by transmitting only a part of the wavelength band of white light emitted by a conventional halogen lamp or the like. can do. For this reason, a special light can be used to display a captured image in which an image of blood having a high absorptivity is emphasized more than in the past. Such display of a captured image is used not only for diagnosis of a living tissue but also for treatment of living tissue. For example, special light may be used to search for concentrated lesions in blood vessels of a living tissue, such as a tumor, and perform a treatment to remove the tumor. When excising the tumorous part, insert the excision treatment tool from the operation part of the endoscope system and project it from the tip surface provided with the illumination window from which the illumination light is emitted and the observation window that receives the light of the image of the imaging subject. While looking at the image taken by the endoscope system, the tumor part is scratched and marked, and then the tumor part is excised using a resection treatment tool.
 しかし、このとき切除した部分では、血液が多量に流出して照明窓や観察窓に付着する場合がある。観察窓に付着した血液の像は撮像画像に表示されるので、観察窓に付着した血液を、先端面に設けた送気口あるいは送水口から流体(液体あるいは気体)を吐出させて観察窓を洗浄することができる。一方、照明窓に血液が付着した場合、生体組織の照明が急激に暗くなり、あるいは真っ暗になり、モニタ画面に表示される撮像画像が急激に暗くなり、あるいは、急激に真っ暗になって観察や診断ができなくなる場合がある。 However, in the cut portion at this time, a large amount of blood may flow out and adhere to the illumination window or the observation window. Since the image of the blood adhering to the observation window is displayed on the captured image, the blood adhered to the observation window is discharged from the air supply port or water supply port provided at the tip end surface to make the observation window It can be washed. On the other hand, when blood adheres to the illumination window, the illumination of the living tissue is rapidly darkened or completely dark, and the captured image displayed on the monitor screen is rapidly darkened or sharply darkened for observation or It may not be possible to diagnose.
 さらに、発光ダイオードを用いた強い光強度の特殊光で生体組織を照明する場合、特殊光の一部の光は、血液の吸光率が高い波長帯域に合わせて光強度分布が設定されるため、照明窓に付着した血液は、上記一部の光を吸収して熱になって温まり、照明窓の表面で乾燥し膜として固着する場合がある。血液が固着すると、照明窓に流体を吐出させても表面に固着した膜を洗浄することはできない。このため、照明窓に付着した血液は、固着する前に洗浄することが必要になる。なお、照明窓の表面に固着する物質は、体腔内に流出した血液に限らず、生体組織から分泌する生体物質や、生体外から体腔内に導入され体腔内に残る外部物質の残渣等の体腔内物質もある。 Furthermore, when a living tissue is illuminated with special light of high light intensity using a light emitting diode, a part of the special light has a light intensity distribution set according to the wavelength band where the absorptivity of blood is high, The blood adhering to the illumination window may absorb the part of the light to become heat and warm up, and may be dried on the surface of the illumination window and fixed as a film. When the blood adheres, even if the fluid is discharged to the illumination window, it is not possible to wash the film adhered to the surface. For this reason, the blood adhering to the illumination window needs to be washed before it is fixed. The substance that adheres to the surface of the illumination window is not limited to blood that has flowed into the body cavity, but is a biological substance that is secreted from living tissue, or a body cavity such as a residue of an external substance introduced from outside the body into the body cavity and remaining in the body cavity. There is also an inner substance.
 そこで、本発明は、体腔内の生体組織を撮像しながら生体組織を処置する際、体腔内物質が内視鏡の先端面の照明窓に付着し撮像画像が見えなくなり診断や処置が困難になることを抑制できる電子内視鏡システムを提供することを目的とする。 Therefore, according to the present invention, when the living tissue is treated while imaging the living tissue in the body cavity, the substance in the body cavity adheres to the illumination window on the distal end surface of the endoscope and the captured image can not be seen and diagnosis and treatment become difficult It is an object of the present invention to provide an electronic endoscope system capable of suppressing the
 本発明の一態様は、体腔内の生体組織を撮像するように構成された電子内視鏡及びプロセッサを備える電子内視鏡システムである。当該電子内視鏡システムは、
 照明光を出射するように構成された光源部と、
 前記電子内視鏡に設けられ、前記照明光で照明された前記生体組織を撮像するように構成された撮像素子と、
 前記プロセッサに設けられ、前記撮像素子で撮像された前記生体組織の撮像画像が、前記撮像画像の画素における異なる画像色成分の値同士の比率を用いた判定条件を満足するか否かの判定を行うように構成された判定部と、前記判定の結果に応じて、前記照明光が含む光成分のうち一部の光成分の単位時間当たりの光量を変更するように前記光源部を制御するように構成された光量変更部と、を備える制御部と、を備える。
 前記判定は、前記撮像素子で撮像された撮像画像が、体腔内の前記生体組織とは別の体腔内物質の像を含む撮像画像であるか否かを、前記比率によって行う判定であり、
 前記判定条件に用いる前記比率は、前記撮像素子の感度波長帯域の中で前記体腔内物質の光反射率が最も高い波長を含む前記撮像画像の注目画像色成分の値に対する、前記注目画像色成分以外の画像色成分の値の比率であり、
 前記光量変更部は、前記体腔内物質の吸光率に応じて定められる前記照明光の光成分を光量制御対象光として前記光成分の光量を変更するように構成されている。
One aspect of the present invention is an electronic endoscope system comprising an electronic endoscope and a processor configured to image living tissue in a body cavity. The electronic endoscope system is
A light source configured to emit illumination light;
An imaging device provided in the electronic endoscope and configured to image the living tissue illuminated by the illumination light;
It is provided in the processor, and it is determined whether a captured image of the living tissue captured by the imaging device satisfies a determination condition using a ratio of values of different image color components in pixels of the captured image. The light source unit is controlled to change a light amount per unit time of a light component of a part of the light components included in the illumination light according to a determination unit configured to perform and a result of the determination. And a control unit including the light amount change unit configured in the above.
The determination is a determination as to whether the captured image captured by the imaging element is a captured image including an image of a body cavity material different from the living tissue in the body cavity based on the ratio.
The ratio used for the determination condition is the image color component of interest with respect to the value of the image color component of interest of the captured image including the wavelength at which the light reflectance of the body cavity material is highest in the sensitivity wavelength band of the imaging element. It is a ratio of values of image color components other than
The light amount changing unit is configured to change the light amount of the light component, with the light component of the illumination light determined according to the absorptivity of the substance in the body cavity as a light amount control target light.
 前記照明光は、複数の光を前記光成分として合成した合成光であり、
 前記光量変更部は、前記光量制御対象光として前記照明光のうち光量を低減する第1光成分と、光量を低減しない第2光成分とに分けて前記第1光成分の光量を低減するように構成され、前記第1光成分を吸光する前記体腔内物質の前記吸光率は、前記第2光成分を吸光する前記体腔内物質の前記吸光率より大きい、ことが好ましい。
 また、前記光量制御対象光の波長は、前記体腔内物質の前記吸光率が最大となる波長を含む、ことが好ましい。
The illumination light is combined light obtained by combining a plurality of lights as the light component,
The light amount changing unit is configured to reduce the light amount of the first light component by dividing it into a first light component for reducing the light amount among the illumination light as the light amount control target light and a second light component for which the light amount is not reduced. Preferably, the absorptivity of the body cavity substance that absorbs the first light component is larger than the absorptivity of the body cavity substance that absorbs the second light component.
Further, it is preferable that the wavelength of the light quantity control target light includes a wavelength at which the absorptivity of the substance in the body cavity is maximum.
 前記判定条件は、前記撮像画像内において、前記比率が所定の閾値より小さい画素数が、許容限界値として予め定めた数より大きいか否かの条件を含む、ことが好ましい。 It is preferable that the determination condition includes a condition whether or not the number of pixels whose ratio is smaller than a predetermined threshold value is larger than a predetermined number as an allowable limit value in the captured image.
 前記撮像素子は、前記生体組織を時系列で撮像するように構成され、
 前記判定条件は、前記撮像画像において、前記比率の時間変化が所定の範囲を超えて大きくなった画素数が、許容限界値として予め定めた数より大きいか否かの条件を含む、ことが好ましい。
The imaging device is configured to image the biological tissue in time series;
It is preferable that the determination condition includes a condition whether or not the number of pixels of which the temporal change of the ratio has become larger than a predetermined range in the captured image is larger than a predetermined number as an allowable limit value. .
 前記撮像素子は、前記生体組織を時系列で撮像するように構成され、
 前記判定条件は、前記撮像画像において、前記比率が所定の閾値より小さい画素数が、予め定めた数より大きい状態が続く継続時間が、許容限界値として予め定めた時間より長いか否かの条件を含む、ことが好ましい。
The imaging device is configured to image the biological tissue in time series;
The determination condition is whether or not the duration in which the number of pixels whose ratio is smaller than a predetermined threshold value is larger than a predetermined number is longer than the predetermined time as the allowable limit value in the captured image. Is preferred.
  前記撮像素子は、前記生体組織を時系列で撮像するように構成され、
 前記判定条件は、前記撮像画像において、前記比率の時間変化が所定の範囲を超えて大きくなった画素数が、予め定めた数より大きい状態が続く継続時間が許容限界値として予め定めた時間より長いか否かの条件を含む、ことが好ましい。
The imaging device is configured to image the biological tissue in time series;
The determination condition is that, in the captured image, the duration time in which the number of pixels whose temporal change of the ratio is increased beyond a predetermined range is larger than a predetermined number continues as an allowable limit value. It is preferable that the condition be long or not.
 前記光量変更部は、前記光量制御対象光の光量を複数の光量レベルに分けて順次段階的に変更し、
 前記判定部は、前記光量制御対象光の変更後の光量に応じて、前記判定条件で用いる前記許容限界値を変更するために、前記光量と前記許容限界値とを対応させた参照テーブルを備える、ことが好ましい。
The light quantity changer divides the light quantity of the light quantity control target light into a plurality of light quantity levels and sequentially changes them in stages.
The determination unit includes a reference table in which the light amount is associated with the allowable limit value in order to change the allowable limit value used in the determination condition according to the light amount after the change of the light amount control target light. Is preferred.
 前記判定条件を満足する場合、前記光量変更部は、前記照明光の全光量に対する前記光量制御対象光の光量の相対比を低くするように前記光源部を制御するように構成されている、ことが好ましい。 When the determination condition is satisfied, the light amount changing unit is configured to control the light source unit to reduce a relative ratio of the light amount of the light amount control target light to the total light amount of the illumination light. Is preferred.
 前記制御部は、前記撮像画像の輝度成分の平均値の低下に応じて、前記光源部が出射する前記照明光全体の光量が増加するように前記光源部を制御するように構成されている自動光量調整部を備え、
 前記判定部は、さらに、前記自動光量調整部により増加した前記照明光全体の光量が予め定めた量を超えたか否かを判定するように構成され、
 前記光量変更部は、前記判定条件を満足し、かつ前記照明光全体の光量が予め定めた量を超えた場合に、前記光量制御対象光の光量を変更するように前記光源部を制御するように構成されている、ことが好ましい。
The control unit is configured to automatically control the light source unit such that the amount of light of the entire illumination light emitted by the light source unit is increased according to a decrease in an average value of luminance components of the captured image. It has a light quantity adjustment unit,
The determination unit is further configured to determine whether or not the light amount of the entire illumination light increased by the automatic light amount adjustment unit exceeds a predetermined amount.
The light amount change unit controls the light source unit to change the light amount of the light amount control target light when the determination condition is satisfied and the light amount of the entire illumination light exceeds a predetermined amount. Preferably, it is configured in
 前記電子内視鏡は、前記照明光を前記生体組織に向けて照明するための照明窓、前記生体組織の像を取り込むための観察窓、及び、前記照明窓及び前記観察窓の表面に向けて流体が吐出するように構成された流体吐出ポートを備えた先端面を有し、
 前記電子内視鏡は、前記流体吐出ポートから前記流体を吐出させるために前記流体を供給するように構成された流体送出機構と接続され、
 前記制御部は、前記流体吐出ポートから前記流体を吐出させるように前記流体送出機構の動作の制御を行うように構成された流体動作制御部を備え、
 前記判定部が前記増加した前記照明光全体の光量が予め定めた量を超えたか否かを判定する前に、前記流体動作制御部は、前記流体吐出ポートから前記流体を吐出させる動作の制御を行うように構成されている、ことが好ましい。
The electronic endoscope includes an illumination window for illuminating the illumination light toward the living tissue, an observation window for capturing an image of the living tissue, and a surface of the illumination window and the observation window. Having a tip surface with a fluid discharge port configured to discharge fluid;
The electronic endoscope is connected with a fluid delivery mechanism configured to supply the fluid to eject the fluid from the fluid ejection port;
The control unit includes a fluid operation control unit configured to control the operation of the fluid delivery mechanism so as to discharge the fluid from the fluid discharge port;
The fluid operation control unit controls the operation of causing the fluid to be discharged from the fluid discharge port before the determination unit determines whether the increased total amount of illumination light has exceeded a predetermined amount. Preferably, it is configured to do.
 前記電子内視鏡は、前記照明光を前記生体組織に向けて照明するための照明窓、前記生体組織の像を取り込むための観察窓、及び、前記照明窓及び前記観察窓の表面に向けて流体が吐出するように構成された流体吐出ポートを備えた先端面を有し、
 前記電子内視鏡は、前記流体吐出ポートから前記流体を吐出させるために前記流体を供給するように構成された流体送出機構と接続され、
 前記制御部は、前記光量変更部が前記光量制御対象光の光量を変更する時に、前記流体吐出ポートから前記流体を吐出させるように前記流体送出機構の動作の制御を行うように構成された流体動作制御部を備える、ことが好ましい。
 前記照明窓は、前記観察窓を挟む2つの場所のそれぞれに設けられ、
 前記流体吐出ポートには、前記照明窓及び前記観察窓のそれぞれに流体を吐出するように構成されている吐出ノズルが設けられている、ことが好ましい。
The electronic endoscope includes an illumination window for illuminating the illumination light toward the living tissue, an observation window for capturing an image of the living tissue, and a surface of the illumination window and the observation window. Having a tip surface with a fluid discharge port configured to discharge fluid;
The electronic endoscope is connected with a fluid delivery mechanism configured to supply the fluid to eject the fluid from the fluid ejection port;
The control unit is configured to control the operation of the fluid delivery mechanism so as to discharge the fluid from the fluid discharge port when the light amount changing unit changes the light amount of the light amount control target light Preferably, an operation control unit is provided.
The illumination window is provided at each of two places sandwiching the observation window,
Preferably, the fluid discharge port is provided with a discharge nozzle configured to discharge fluid to each of the illumination window and the observation window.
 前記制御部は、前記光量制御対象光の光強度を変更することにより、前記光量制御対象光の単位時間当たりの光量を変更するように構成されている、ことが好ましい。 It is preferable that the control unit is configured to change the light amount per unit time of the light amount control target light by changing the light intensity of the light amount control target light.
 前記プロセッサは、前記撮像画像を画像処理するように構成された画像処理部を備え、
 前記画像処理部は、前記光量制御対象光の光量の変更後に前記撮像素子で撮像した前記撮像画像中の、前記光量制御対象光の波長帯域を含む波長帯域の画像色成分に対するゲイン調整量を、前記光量制御対象光の光量の変化量に応じて変更するように構成されている、ことが好ましい。
The processor includes an image processing unit configured to perform image processing on the captured image;
The image processing unit is configured to adjust a gain adjustment amount for an image color component of a wavelength band including the wavelength band of the light amount control target light in the captured image captured by the imaging device after changing the light amount of the light amount control target light. It is preferable that it is configured to change according to the amount of change of the light quantity of the light quantity control target light.
 前記撮像画像の画像色成分の1つである画像色成分Aは、前記光源部から出射する複数の光のうち、前記光量制御対象光の波長帯域の他に、少なくとも1つの別の光の波長帯域を、前記画像色成分Aの波長帯域として含み、
 前記光量変更部は、前記光量制御対象光の光量を変更したとき、前記画像色成分Aの値の変化を抑制するために、前記別の光の単位時間当たりの光量を変更するように構成されている、ことが好ましい。
The image color component A, which is one of the image color components of the captured image, is a wavelength of at least one other light in addition to the wavelength band of the light quantity control target light among the plurality of lights emitted from the light source unit A band is included as a wavelength band of the image color component A,
The light quantity changing unit is configured to change the light quantity per unit time of the other light in order to suppress a change in the value of the image color component A when the light quantity of the light quantity control target light is changed. Is preferred.
 前記電子内視鏡システムは、前記プロセッサに接続された、前記撮像画像を表示するように構成されているモニタを備え
 前記制御部は、前記撮像画像の前記画像色成分が前記判定条件を満足する場合、前記照明光を前記生体組織に向けて照明するための照明窓に前記体腔内物質が付着した可能性がある旨の情報を報知するために、前記モニタに前記情報を送信するように構成された報知制御部を備える、ことが好ましい。
The electronic endoscope system includes a monitor connected to the processor and configured to display the captured image. The control unit determines that the image color component of the captured image satisfies the determination condition. In the case, the monitor is configured to transmit the information to notify information indicating that the intracavitary substance may be attached to an illumination window for illuminating the illumination light toward the living tissue. It is preferable that the information control unit be provided.
 前記報知制御部による前記情報報知から所定時間経過後、前記光量変更部は、前記光量制御対象光の光量の変更を行うように構成されている、ことが好ましい。 It is preferable that the light amount change unit is configured to change the light amount of the light amount control target light after a predetermined time has elapsed from the information notification by the notification control unit.
 上述の電子内視鏡システムによれば、体腔内の生体組織を撮像しながら生体組織を処置する際、体腔内物質が内視鏡の先端面の照明窓に付着し撮像画像が見えなくなり診断や処置が困難になることを抑制できる。 According to the above-mentioned electronic endoscope system, when the living tissue is treated while imaging the living tissue in the body cavity, the substance in the body cavity adheres to the illumination window of the distal end surface of the endoscope and the captured image disappears and diagnosis or It can control that treatment becomes difficult.
一実施形態である電子内視鏡システムの外観斜視図である。FIG. 1 is an external perspective view of an electronic endoscope system according to an embodiment. 一実施形態である電子内視鏡システムの構成を示すブロック図である。It is a block diagram showing composition of an electronic endoscope system which is one embodiment. 図2に示す内視鏡システムの光源部の構成を模式的に説明する図である。It is a figure which illustrates typically the structure of the light source part of the endoscope system shown in FIG. 一実施形態の電子内視鏡の先端部の先端面の一例を示す図である。It is a figure which shows an example of the front end surface of the front-end | tip part of the electronic endoscope of one Embodiment. 図2に示す電子内視鏡システムで用いる特殊光のスペクトル波形の一例を示図である。It is a figure which shows an example of the spectrum waveform of the special light used with the electronic endoscope system shown in FIG. 図2に示す電子内視鏡システムで用いる白色光のスペクトル波形の一例を示す図である。It is a figure which shows an example of the spectrum waveform of the white light used with the electronic endoscope system shown in FIG. 図2に示す電子内視鏡システムのシステムコントローラの構成を説明するブロック図である。It is a block diagram explaining the structure of the system controller of the electronic endoscope system shown in FIG. 図2に示す電子内視鏡システムの固体撮像素子に設けられる原色色フィルタの透過率のスペクトル波形の一例を示す図である。It is a figure which shows an example of the spectrum waveform of the transmittance | permeability of the primary color filter provided in the solid-state image sensor of the electronic endoscope system shown in FIG. 血液の吸光率のスペクトル波形を示す図である。It is a figure which shows the spectrum waveform of the absorptivity of the blood. 一実施形態の電子内視鏡システムのシステムコントローラの構成の一例を示すブロック図である。It is a block diagram showing an example of composition of a system controller of an electronic endoscope system of one embodiment. 一実施形態の電子内視鏡システムのシステムコントローラの構成の一例を示すブロック図である。It is a block diagram showing an example of composition of a system controller of an electronic endoscope system of one embodiment.
 以下、実施形態の電子内視鏡システムについて図面を参照しながら説明する。
 図1は、一実施形態である電子内視鏡システム1の外観斜視図であり、図2は、電子内視鏡システム1の構成を示すブロック図である。図1に示す電子内視鏡システム1は、医療用に特化されたシステムであり、電子内視鏡(以降、電子スコープという)100、プロセッサ200、光源装置300、モニタ400、を主に備える。電子スコープ100、光源装置300、及びモニタ400は、それぞれプロセッサ200に接続される。なお、光源装置300とプロセッサ200とは別体で構成されているが、光源装置300はプロセッサ200内に一体的に設けられて構成されてもよい。
Hereinafter, the electronic endoscope system of the embodiment will be described with reference to the drawings.
FIG. 1 is an external perspective view of an electronic endoscope system 1 according to an embodiment, and FIG. 2 is a block diagram showing the configuration of the electronic endoscope system 1. The electronic endoscope system 1 shown in FIG. 1 is a system specialized for medical use, and mainly includes an electronic endoscope (hereinafter referred to as an electronic scope) 100, a processor 200, a light source device 300, and a monitor 400. . The electronic scope 100, the light source device 300, and the monitor 400 are connected to the processor 200, respectively. Although the light source device 300 and the processor 200 are separately provided, the light source device 300 may be integrally provided in the processor 200.
 プロセッサ200は、図2に示すように、システムコントローラ21及びタイミングコントローラ22を備えている。システムコントローラ21は、図示されないメモリに記憶された各種プログラムを実行し、電子内視鏡システム1全体を統合的に制御する制御手段であり、ソフトウェアあるいはハードウェアで構成されている。また、システムコントローラ21は、操作パネル24に接続されている。システムコントローラ21は、操作パネル24に入力される術者からの指示に応じて、電子内視鏡システム1の各動作及び各動作のためのパラメータを変更する。術者による入力指示には、例えば電子内視鏡システム1の観察モードの切替指示が含まれる。観察モードには、白色光を照明光として観察する通常観察モード、特殊光を照明光として観察する特殊観察モードがある。
 タイミングコントローラ22は、各部の動作のタイミングを調整するクロックパルスを電子内視鏡システム1内の各回路に出力する。
The processor 200 includes a system controller 21 and a timing controller 22 as shown in FIG. The system controller 21 is a control unit that executes various programs stored in a memory (not shown) and integrally controls the entire electronic endoscope system 1, and is configured by software or hardware. Further, the system controller 21 is connected to the operation panel 24. The system controller 21 changes each operation of the electronic endoscope system 1 and parameters for each operation according to an instruction from the operator input to the operation panel 24. The input instruction by the operator includes, for example, an instruction to switch the observation mode of the electronic endoscope system 1. The observation modes include a normal observation mode in which white light is observed as illumination light and a special observation mode in which special light is observed as illumination light.
The timing controller 22 outputs clock pulses for adjusting the timing of operation of each unit to each circuit in the electronic endoscope system 1.
 光源装置300は、図2に示すように、光源部310及び集光レンズ350を有する。図3は、光源部310の構成を模式的に説明する図である。図3に示すように、光源部310は、4つの光源ユニット312~315と、3つの光学素子333~335、コリメートレンズ322~325、及び光源駆動回路340、を備える。
 光源駆動回路340は、システムコントローラ21の制御信号に従って、光源ユニット312~315が制御された光強度で駆動するための駆動電流を生成し、各光源ユニットに送る。
The light source device 300 includes a light source unit 310 and a condenser lens 350, as shown in FIG. FIG. 3 is a diagram schematically illustrating the configuration of the light source unit 310. As shown in FIG. As shown in FIG. 3, the light source unit 310 includes four light source units 312 to 315, three optical elements 333 to 335, collimating lenses 322 to 325, and a light source driving circuit 340.
The light source drive circuit 340 generates a drive current for driving the light source units 312 to 315 with the controlled light intensity in accordance with the control signal of the system controller 21 and sends it to each light source unit.
 光源ユニット312~315は、所定の色の波長帯域の光を射出する発光ダイオード(LED:Light Emitting Diode)を含む。
 コリメートレンズ322~325は、各光源ユニット312~315のぞれぞれの前面の、出射光の光路上に配置され、出射光を平行光にする。
The light source units 312 to 315 include light emitting diodes (LEDs: Light Emitting Diodes) that emit light of a wavelength band of a predetermined color.
The collimator lenses 322 to 325 are disposed on the light path of the emitted light on the front surface of each of the light source units 312 to 315, and convert the emitted light into parallel light.
 光学素子333~335は、入射光を透過し、あるいは反射する機能を有する。光学素子332~335は、例えばダイクロイックミラーあるいはダイクロイックプリズムが用いられる。光学素子333~335は、入射した光のうち、光学素子333~335それぞれにおいて波長特性として設定される波長帯域の光成分を反射し、残りの波長帯域の光成分は透過させる。光学素子333~335は、光源ユニット312~315のそれぞれの射出する光の波長帯域に応じて設定された波長特性を有することにより、光学素子333~335で設定された波長帯域の光が合波され1つの照明光となる。光源ユニット312は、例えば、赤色の波長帯域(例えば、波長が620~680nm)の光を射出する赤色LEDであり、光源ユニット313は、青色の波長帯域(例えば、波長が430~470nm)の光を射出する青色LED313aと、緑色蛍光体313bとを有している。緑色蛍光体313bは、青色LED313aから射出された青色LED光によって励起され、緑色の波長帯域(例えば、波長が470~600nm)の蛍光を発する。光源ユニット314は、青色の波長帯域(例えば、波長が430~470nm)の光を射出する青色LEDを含む。光源ユニット315は、紫色の波長帯域(例えば、波長が395~435nm)の光を射出する紫色LEDを含む。紫色の波長帯域は、波長415nmを少なくとも含む。 The optical elements 333 to 335 have a function of transmitting or reflecting incident light. The optical elements 332 to 335 use, for example, a dichroic mirror or a dichroic prism. The optical elements 333 to 335 reflect the light component of the wavelength band set as the wavelength characteristic in each of the optical elements 333 to 335 among the incident light, and transmit the light components of the remaining wavelength bands. The optical elements 333 to 335 have wavelength characteristics set according to the wavelength bands of the light emitted from the light source units 312 to 315, so that the light of the wavelength band set by the optical elements 333 to 335 is multiplexed. It becomes one illumination light. The light source unit 312 is, for example, a red LED that emits light in a red wavelength band (for example, a wavelength of 620 to 680 nm), and the light source unit 313 is light in a blue wavelength band (for example, a wavelength of 430 to 470 nm) And a green phosphor 313b. The green phosphor 313b is excited by the blue LED light emitted from the blue LED 313a, and emits fluorescence in a green wavelength band (for example, a wavelength of 470 to 600 nm). The light source unit 314 includes a blue LED that emits light in a blue wavelength band (for example, a wavelength of 430 to 470 nm). The light source unit 315 includes a purple LED that emits light in a purple wavelength band (eg, a wavelength of 395 to 435 nm). The purple wavelength band at least includes the wavelength 415 nm.
 このような光の波長帯域に応じて設定された波長特性を備える光学素子333~335の各位置で、透過光と反射光を合成する。したがって、光源部310では、複数の光源ユニットから射出した光が、所望の波長帯域を有する光に合成されて照明光として光源部310から出射する。光源駆動回路340は、通常観察モードで用いる白色光を照明光とする場合と、特殊観察モードで用いる特殊光を照明光とする場合では、光源ユニット312~315の射出する光の光強度を変更するように構成される。
 なお、光源部310は、図3に示すように、光学素子333~335が直列に並んだ構成であるが、この構成に限定されない。4つの光源ユニット312~315から射出される光が1つの照明光になるように合成される限りにおいて、光源ユニット312~315及び光学素子333~335の配置等の構成は、特に限定されない。
 このように、照明光は、複数の光を光成分として合成した合成光である。
The transmitted light and the reflected light are combined at each position of the optical elements 333 to 335 having wavelength characteristics set according to such a wavelength band of light. Therefore, in the light source unit 310, the light emitted from the plurality of light source units is combined with the light having a desired wavelength band and emitted from the light source unit 310 as illumination light. The light source drive circuit 340 changes the light intensity of the light emitted from the light source units 312 to 315 in the case where the white light used in the normal observation mode is the illumination light and the special light used in the special observation mode is the illumination light. Configured to
Although the light source unit 310 has a configuration in which the optical elements 333 to 335 are arranged in series as shown in FIG. 3, the present invention is not limited to this configuration. As long as light emitted from the four light source units 312 to 315 is combined into one illumination light, the configuration of the arrangement of the light source units 312 to 315 and the optical elements 333 to 335 is not particularly limited.
Thus, illumination light is synthetic light which compounded a plurality of lights as a light component.
 図2に示すように、光源部310から出射した照明光Lは、集光レンズ350により、複数の光ファイバの束によって構成された後述するLCB(Light Carrying Bundle)11の入射端面に集光されてLCB11内に入射される。 As shown in FIG. 2, the illumination light L emitted from the light source unit 310 is condensed by the condenser lens 350 on the incident end face of a light carrying bundle (LCB) 11 described later, which is formed of a bundle of plural optical fibers. And enter the LCB 11.
 電子スコープ100は、図1に示すように、接続部50と、操作部52と、挿入部54と、接続部50と操作部52とを接続するケーブル51と、を主に有する。挿入部54は、操作部52と挿入部50の先端部56とを接続する可撓管58を備える。可撓管58の内部には、LCB11、水や空気等の流体を送る送気送水管、処置具導入管、及び信号線等が設けられている。処置具導入管は、生体組織を処置する(例えば、切断除去する)ための処置具を操作部52から挿入し先端部56から突出させて生体組織を処置するために処置具を通す管である。信号線は、後述する固体撮像素子14からの撮像画像信号を送信する伝送線及びプロセッサ200からの制御信号を固体撮像素子14に送信する制御線を含む。
 電子スコープ100の、操作部52の先端側の部分は、人体内部に挿入するために可撓性を有する挿入部54となっている。挿入部54の先端近傍には、挿入部54の基端に連結された屈曲部60が設けられ、屈曲部60は、操作部52における遠隔操作に応じて屈曲する。屈曲部60の屈曲機構は、一般的な内視鏡に組み込まれている周知の機構である。屈曲構造は、操作部52に設けられた湾曲操作ノブの回転操作に連動した操作ワイヤの牽引によって屈曲部60を屈曲させるものである。屈曲部60の先端には、固体撮像素子14を備えた先端部56が設けられている。
As shown in FIG. 1, the electronic scope 100 mainly includes a connection portion 50, an operation portion 52, an insertion portion 54, and a cable 51 connecting the connection portion 50 and the operation portion 52. The insertion portion 54 includes a flexible tube 58 connecting the operation portion 52 and the distal end portion 56 of the insertion portion 50. Inside the flexible tube 58, an LCB 11, an air / water tube for sending a fluid such as water or air, a treatment instrument introduction tube, a signal line and the like are provided. The treatment instrument introduction tube is a tube for inserting a treatment instrument for treating (for example, cutting and removing) living tissue from the operation unit 52 and projecting it from the tip portion 56 to treat the living tissue. . The signal line includes a transmission line for transmitting a captured image signal from a solid-state imaging device 14 described later and a control line for transmitting a control signal from the processor 200 to the solid-state imaging device 14.
The distal end portion of the operation unit 52 of the electronic scope 100 is a flexible insertion portion 54 for insertion into the human body. In the vicinity of the distal end of the insertion portion 54, a bending portion 60 connected to the proximal end of the insertion portion 54 is provided, and the bending portion 60 bends in response to the remote control in the operation portion 52. The bending mechanism of the bending portion 60 is a known mechanism incorporated in a general endoscope. The bending structure is to bend the bending portion 60 by pulling the operation wire interlocked with the rotation operation of the bending operation knob provided in the operation portion 52. At the tip of the bending portion 60, a tip portion 56 provided with a solid-state imaging device 14 is provided.
 電子スコープ100の先端部56には、接続部50から先端部56にかけての略全長に渡って配置されたLCB11の照明光出射端がある。
 先端部56には、図2に示されるように、LCB11の照明光出射端の前方に配光レンズが設けられ、配光レンズの生体組織側の前面は照明光を出射する照明窓12となっている。また、先端部56には、生体組織の像を結像する対物レンズが設けられ、対物レンズの生体組織側の前面は、生体組織の像の光を受け入れる観察窓13となっている。さらに、先端部56には、結像した像を受光する固体撮像素子14、及び固体撮像素子14から出力した画像信号を増幅する図示されないアンプ等が設けられている。
The distal end portion 56 of the electronic scope 100 has an illumination light emitting end of the LCB 11 disposed over substantially the entire length from the connection portion 50 to the distal end portion 56.
As shown in FIG. 2, the light distribution lens is provided in front of the illumination light emission end of the LCB 11 at the distal end portion 56, and the front surface on the living tissue side of the light distribution lens is the illumination window 12 for emitting illumination light. ing. Further, the distal end portion 56 is provided with an objective lens for forming an image of a living tissue, and the front surface on the living tissue side of the objective lens is an observation window 13 for receiving light of the image of the living tissue. Further, the tip end portion 56 is provided with a solid-state imaging device 14 for receiving the formed image, and an amplifier (not shown) for amplifying an image signal output from the solid-state imaging device 14.
 LCB11内に入射した照明光は、LCB11内を伝播し、LCB11の照明光出射端から出射し、配光レンズで構成される照明窓12を介して生体組織の被写体に照明光として照明する。照明窓12から出射した照明光の、被写体からの戻り光は、対物レンズで構成される観察窓13を介して固体撮像素子14の受光面上で光学像を結ぶ。
 なお、光源装置300の光源部310は、コンパクトな構成である場合、電子スコープ100の先端部56に内臓されてもよい。この場合、照明光を光源部310から先端部56に導光するLCB11及び集光レンズ350は不要である。
The illumination light that has entered the LCB 11 propagates in the LCB 11, exits from the illumination light output end of the LCB 11, and illuminates the subject of the biological tissue as illumination light through the illumination window 12 configured with a light distribution lens. The return light from the subject of the illumination light emitted from the illumination window 12 forms an optical image on the light receiving surface of the solid-state imaging device 14 through the observation window 13 constituted by the objective lens.
The light source unit 310 of the light source device 300 may be embedded in the tip end portion 56 of the electronic scope 100 when the configuration is compact. In this case, the LCB 11 and the condenser lens 350 for guiding the illumination light from the light source unit 310 to the distal end portion 56 are unnecessary.
 図4は、先端部56の先端面57の一例を示す図である。先端面57には、LCB11の先端の前方に設けられた配光レンズで構成された照明窓12が2つ設けられ、さらに、照明窓12の間に挟まれるように、対物レンズで構成された観察窓13が設けられている。また、先端面57には、処置具を先端面57から突出させる処置具用開口62、及び、照明窓12及び観察窓13を洗浄するための流体を吐出させる送気送水ポート64(流体吐出ポート)を備える。送気送水ポート64は、可撓管58内の送気送水管を介して操作部52に接続された流体送出機構(図10参照)から流体の供給を受けて、流体を吐出させる部分である。送気送水ポート64には、具体的には、3つの吐出ノズルがあり、吐出ノズルは、2つの照明窓12と1つの観察窓13のそれぞれに、水、空気を吹き付けて洗浄するように構成されている。
 また、図4に示す先端面57に代えて、送気送水ポート64が、空気を吐出する送気ポートと水を吐出する送水ポートとが別べつに設けられてもよい。
FIG. 4 is a view showing an example of the distal end surface 57 of the distal end portion 56. As shown in FIG. On the front end surface 57, two illumination windows 12 composed of light distribution lenses provided in front of the tip of the LCB 11 are provided, and further, they are composed of objective lenses so as to be sandwiched between the illumination windows 12 An observation window 13 is provided. In addition, a treatment tool opening 62 for causing the treatment tool to protrude from the tip end surface 57, and an air / water supply port 64 (a fluid discharge port for discharging a fluid for cleaning the illumination window 12 and the observation window 13) ). The air / water supply port 64 is a portion that receives the supply of fluid from the fluid delivery mechanism (see FIG. 10) connected to the operation unit 52 via the air / water supply pipe in the flexible tube 58 and discharges the fluid. . Specifically, the air / water supply port 64 has three discharge nozzles, and the discharge nozzles are configured to spray and wash water and air on each of the two illumination windows 12 and one observation window 13. It is done.
Further, instead of the end face 57 shown in FIG. 4, the air / water supply port 64 may be provided separately from the air supply port for discharging air and the water supply port for discharging water.
 固体撮像素子14は、ベイヤ型画素配置を有する単板式カラー撮像素子である。固体撮像素子14は、受光面上の各画素で結像した光学像を光量に応じた電荷として蓄積して、R(Red)、G(Green)、B(Blue)の画像信号を生成して出力する。なお、固体撮像素子14は、CCD(Charge Coupled Device)イメージセンサ、あるいは、CMOS(Complementary Metal Oxide Semiconductor)イメージセンサである。あるいは、上記イメージセンサ以外の撮像装置であってもよい。固体撮像素子14の撮像画像の画像色成分における波長帯域を定める色フィルタが、固体撮像素子14の各受光位置の前方に設けられている。色フィルタは、例えば、赤(R)、緑(G)、青(B)の原色系フィルタが用いられる。固体撮像素子14は、タイミングコントローラ22から送信されるクロックパルスに従ったタイミングで生体組織を繰り返し撮像する。すなわち、固体撮像素子14は、生体組織を時系列に撮像するように構成される。言い換えると固体撮像素子14は、生体組織の動画を得るように構成される。 The solid-state imaging device 14 is a single-plate color imaging device having a Bayer-type pixel arrangement. The solid-state imaging device 14 accumulates an optical image formed by each pixel on the light receiving surface as an electric charge according to the light quantity, and generates image signals of R (Red), G (Green), and B (Blue). Output. The solid-state imaging device 14 is a charge coupled device (CCD) image sensor or a complementary metal oxide semiconductor (CMOS) image sensor. Alternatively, an imaging device other than the image sensor may be used. A color filter that defines a wavelength band in an image color component of a captured image of the solid-state imaging device 14 is provided in front of each light receiving position of the solid-state imaging device 14. As color filters, for example, primary color filters of red (R), green (G) and blue (B) are used. The solid-state imaging device 14 repeatedly images the living tissue at timing according to the clock pulse transmitted from the timing controller 22. That is, the solid-state imaging device 14 is configured to image a living tissue in time series. In other words, the solid-state imaging device 14 is configured to obtain a moving image of a living tissue.
 電子スコープ100の接続部50内には、図2に示すようにドライバ信号処理回路15及びメモリ16が備えられている。ドライバ信号処理回路15には、生体組織の画像信号がフレーム周期で固体撮像素子14から入力される。フレーム周期は、例えば、1/30秒である。ドライバ信号処理回路15は、固体撮像素子14から入力される画像信号に対して所定の処理を施してプロセッサ200の前段信号処理回路26に出力する。 In the connection unit 50 of the electronic scope 100, a driver signal processing circuit 15 and a memory 16 are provided as shown in FIG. The driver signal processing circuit 15 receives an image signal of a living tissue from the solid-state imaging device 14 in a frame cycle. The frame period is, for example, 1/30 seconds. The driver signal processing circuit 15 performs predetermined processing on the image signal input from the solid-state imaging device 14, and outputs the processed signal to the pre-stage signal processing circuit 26 of the processor 200.
 ドライバ信号処理回路15はまた、メモリ16にアクセスして電子スコープ100の固有情報を読み出す。メモリ16に記録される電子スコープ100の固有情報には、例えば、固体撮像素子14の画素数や感度、動作可能なフレームレート、型番等が含まれる。ドライバ信号処理回路15は、メモリ16から読み出された固有情報をシステムコントローラ21に出力する。 The driver signal processing circuit 15 also accesses the memory 16 to read out the unique information of the electronic scope 100. The unique information of the electronic scope 100 recorded in the memory 16 includes, for example, the number of pixels and sensitivity of the solid-state imaging device 14, an operable frame rate, and a model number. The driver signal processing circuit 15 outputs the unique information read from the memory 16 to the system controller 21.
 システムコントローラ21は、電子スコープ100の固有情報に基づいて各種演算を行い、制御信号を生成する。システムコントローラ21は、生成された制御信号を用いて、プロセッサ200に接続されている電子スコープ100に適した処理がなされるようにプロセッサ200内の各種回路の動作やタイミングを制御する。 The system controller 21 performs various operations based on the unique information of the electronic scope 100 to generate a control signal. The system controller 21 controls the operation and timing of various circuits in the processor 200 so that processing suitable for the electronic scope 100 connected to the processor 200 is performed using the generated control signal.
 タイミングコントローラ22は、システムコントローラ21によるタイミング制御に従って、ドライバ信号処理回路15にクロックパルスを供給する。ドライバ信号処理回路15は、タイミングコントローラ22から供給されるクロックパルスに従って、固体撮像素子14を、プロセッサ200側で処理される映像のフレームレートに同期したタイミングで駆動制御する。 The timing controller 22 supplies clock pulses to the driver signal processing circuit 15 according to the timing control by the system controller 21. The driver signal processing circuit 15 drives and controls the solid-state imaging device 14 at timing synchronized with the frame rate of the image processed on the processor 200 side according to the clock pulse supplied from the timing controller 22.
 前段信号処理回路26は、ドライバ信号処理回路15から1フレーム周期で入力される撮像画像の画像信号に対してデモザイク処理、マトリックス演算、ゲイン調整、色バランス処理等の所定の画像処理を施して、画像メモリ27に出力する。 The pre-stage signal processing circuit 26 performs predetermined image processing such as demosaicing, matrix calculation, gain adjustment, and color balance processing on the image signal of the captured image input from the driver signal processing circuit 15 in one frame cycle, It is output to the image memory 27.
 画像メモリ27は、前段信号処理回路26から入力される画像信号をバッファし、タイミングコントローラ22によるタイミング制御に従い、後段信号処理回路28に出力する。 The image memory 27 buffers an image signal input from the front stage signal processing circuit 26, and outputs the image signal to the rear stage signal processing circuit 28 in accordance with timing control by the timing controller 22.
 後段信号処理回路28は、画像メモリ27から入力される画像信号を処理してモニタ表示用の画面データを生成し、生成されたモニタ表示用の画面データを所定のビデオフォーマット信号に変換する。変換されたビデオフォーマット信号は、モニタ400に出力される。これにより、電子スコープ100で時系列で撮像された生体組織体の動画がモニタ400の表示画面に表示される。 The post-stage signal processing circuit 28 processes the image signal input from the image memory 27 to generate screen data for monitor display, and converts the generated screen data for monitor display into a predetermined video format signal. The converted video format signal is output to the monitor 400. As a result, the moving image of the biological tissue taken in time series by the electronic scope 100 is displayed on the display screen of the monitor 400.
 電子内視鏡システム1は、生体組織の観察のために、通常観察モードと特殊観察モードを含む複数の観察モードを有している。各観察モードは、観察する生体組織に応じて手動又は自動で切り替えられる。例えば、生体組織を白色光で照明して観察したい場合は、例えば操作パネル24を通した入力指示により、観察モードが通常観察モードに切り替えられる。白色光は、可視光帯域においてフラットな分光強度分布を有する光の他に、分光強度分布はフラットではなく、複数の波長帯域の光が混色されている擬似白色光を含む。また、生体組織を特殊光で照明することによって血管等の特定の生体組織が強調された撮影画像を得たい場合は、例えば操作パネル24を通した入力指示により、観察モードが特殊観察モードに切り替えられる。 The electronic endoscope system 1 has a plurality of observation modes including a normal observation mode and a special observation mode for observing a living tissue. Each observation mode is switched manually or automatically according to the living tissue to be observed. For example, when it is desired to illuminate and observe a living tissue with white light, the observation mode is switched to the normal observation mode by, for example, an input instruction through the operation panel 24. In addition to light having a flat spectral intensity distribution in the visible light band, white light includes pseudo white light in which light of a plurality of wavelength bands is mixed, not having a flat spectral intensity distribution. When it is desired to obtain a photographed image in which a specific biological tissue such as a blood vessel is emphasized by illuminating the biological tissue with special light, the observation mode is switched to the special observation mode by, for example, an input instruction through the operation panel 24. Be
 図5は、特殊観察モードで用いる特殊光のスペクトル波形の一例を示す図である。図6は、通常観察モードで用いる白色光、具体的には、擬似白色光のスペクトル波形の一例を示す図である。図5,6に示すように、395~435nmの波長帯域を有する紫色の光Lvと、430~470nmの波長帯域を有する青色の光Lbと、470~600nmの波長帯域を有する緑色の光Lgと、620~680nmの波長帯域を有する赤色の光Lrが合成して得られる照明光である。図5に一例として示す特殊光は、紫色の光Lvの光強度が、他の光の光強度に比べて圧倒的に強い。これにより、血管に含まれる410~420nmに大きな吸光率を有し、特に415nmで最大の吸光率を有する血液(ヘモグロビン)を強調することができ、すなわち、血管の像を強調することができる。
 一方、図6に一例として示す擬似白色光では、紫色の光Lvの光強度は、上記特殊光における紫色の光Lvの光強度に比べて低く、その代わり、青色の光Lbの光強度が高く、上記特殊光における青色の光Lbの光強度に比べて高くなっている。図6に示すスペクトル波形の光は、固体撮像素子14が、固体撮像素子14に設けられる色フィルタを透過した光を受光したときに得られる赤色、緑色、及び青色の信号レベルが略同一になるように、各光の光強度が調整されている。
 このような特殊光あるいは擬似白色光は、光源ユニット312~315の射出する光の単位時間あたりの光量を調整することにより変更することができる。単位時間あたりの光量の調整は、例えば、光強度の調整、あるいは、照明光がパルス点灯の場合は、照射時間の調整により行われる。
FIG. 5 is a diagram showing an example of a spectral waveform of special light used in the special observation mode. FIG. 6 is a diagram showing an example of a spectral waveform of white light used in the normal observation mode, specifically, pseudo white light. As shown in FIGS. 5 and 6, purple light Lv having a wavelength band of 395 to 435 nm, blue light Lb having a wavelength band of 430 to 470 nm, and green light Lg having a wavelength band of 470 to 600 nm , And illumination light obtained by combining red light Lr having a wavelength band of 620 to 680 nm. In the special light shown as an example in FIG. 5, the light intensity of the purple light Lv is overwhelmingly stronger than the light intensities of the other lights. This makes it possible to emphasize blood (hemoglobin) having a large absorptivity at 410 to 420 nm, particularly at 415 nm, contained in blood vessels, ie, to enhance the image of a blood vessel.
On the other hand, in the pseudo white light shown as an example in FIG. 6, the light intensity of the purple light Lv is lower than the light intensity of the purple light Lv in the special light, and instead, the light intensity of the blue light Lb is high The light intensity of the special light is higher than the light intensity of the blue light Lb. The light of the spectral waveform shown in FIG. 6 has substantially the same red, green and blue signal levels obtained when the solid-state imaging device 14 receives the light transmitted through the color filter provided in the solid-state imaging device 14 Thus, the light intensity of each light is adjusted.
Such special light or pseudo white light can be changed by adjusting the amount of light emitted from the light source units 312 to 315 per unit time. The adjustment of the light amount per unit time is performed, for example, by adjusting the light intensity, or by adjusting the irradiation time when the illumination light is pulse lighting.
 このような電子スコープ100を用いて体腔内の生体組織を撮像して生体組織を観察し、処置するとき、体腔内物質が照明窓12に付着して固着する場合がある。以下の説明では、血液を体腔内物質の代表例として説明する。
 例えば、電子内視鏡システム1を用いて、体腔内の血管が集中する腫瘍部分の位置を見つけ出して観察して処置具を用いて腫瘍部分を処置するとき、特殊光を照明光とする特殊観察モードが用いられる。特殊観察モードでは、生体組織の正常部と病変部(腫瘍部分)を区別できる特殊光を照明光とする。このとき、生体組織を例えば切除等の処置をするので血液が体腔内に流出して先端部56の先端面57に付着し易い。先端面57の観察窓13に付着した血液は、撮像画像に反映されるため、血液の付着の有無の判断は可能である。観察窓13に血液が付着していることが確認されると、直ぐに送気送水ポート64から水や空気等の流体を吐出させて表面を洗浄し血液を取り除くことができる。しかし、照明窓12に血液が付着した場合、血液の付着は確認され難いため、血液が照明窓12の表面で凝固し凝着するまで放置される場合がある。一旦、血液が凝着すると、送気送水ポート64から水や空気等の流体を吐出させて照明窓12の表面を洗浄しても、凝着した血液を取り除くことはできない。特に、特殊観察モードで用いる特殊光は、血液の吸光が最も高い波長帯域を有する紫色の光Lvの光強度を擬似白色光における紫色の光Lvの光強度を高くしている場合が多いので、照明窓12に付着した血液は、紫色の光Lvを吸収して、観察窓13に付着した血液よりも早期に凝固し易い。このため、照明窓12に付着する可能性が高い場合、照明窓12に血液が付着した可能性が高いことを早期に判定して、照明窓12の表面を洗浄することが好ましい。
When imaging a living tissue in a body cavity using such an electronic scope 100 to observe and treat the living tissue, a body cavity material may adhere to the illumination window 12 and be fixed. In the following description, blood is described as a representative example of a substance in a body cavity.
For example, when using the electronic endoscope system 1 to find and observe the position of a tumor portion where blood vessels are concentrated in a body cavity, and treat the tumor portion using a treatment tool, special observation using special light as illumination light The mode is used. In the special observation mode, special light that can distinguish between a normal part and a lesion part (tumor part) of a living tissue is used as illumination light. At this time, since the living tissue is treated, for example, by excision, blood easily flows into the body cavity and adheres to the distal end surface 57 of the distal end portion 56. The blood adhering to the observation window 13 of the distal end surface 57 is reflected on the captured image, so it is possible to judge the presence or absence of the blood adhesion. When it is confirmed that the blood adheres to the observation window 13, it is possible to discharge the fluid such as water or air from the air / water supply port 64 immediately to wash the surface and remove the blood. However, when blood adheres to the illumination window 12, it is difficult to confirm the adhesion of the blood, so the blood may be left until it coagulates and adheres on the surface of the illumination window 12. Once the blood has condensed, even if the fluid such as water or air is discharged from the air / water supply port 64 to wash the surface of the illumination window 12, the coagulated blood can not be removed. In particular, the special light used in the special observation mode often makes the light intensity of the purple light Lv having the wavelength band where the light absorption of blood is the highest the light intensity of the purple light Lv in the pseudo white light, The blood adhering to the illumination window 12 absorbs purple light Lv and tends to coagulate earlier than the blood adhering to the observation window 13. For this reason, when the possibility of adhering to the illumination window 12 is high, it is preferable to determine early that the possibility that blood has adhered to the illumination window 12 and to wash the surface of the illumination window 12.
 電子内視鏡システム1は、照明窓12の表面に血液が付着しても早期に血液を取り除くことができるようにするために、照明窓12に血液が付着する可能性が高い場合を早期に判定することができる構成を備える。すなわち、電子内視鏡システム1は、体腔内の生体組織を撮像しながら生体組織を処置する際、体腔内物質である血液が先端面57の照明窓12に付着し固着することで撮像画像が不良になることを抑制する構成を備える。 The electronic endoscope system 1 has a high possibility that blood may adhere to the illumination window 12 so that blood can be removed early even if blood adheres to the surface of the illumination window 12 It has a configuration that can be determined. That is, when imaging the living tissue in the body cavity while treating the living tissue, the electronic endoscope system 1 adheres and adheres the blood which is the body cavity material to the illumination window 12 of the distal end surface 57, thereby capturing the captured image. It has the composition which controls becoming defective.
 図7は、プロセッサ200のシステムコントローラ21の構成を説明する図である。
 図7に示すように、システムコントローラ(制御部)21は、電子内視鏡システム1の各部分の動作を制御管理する制御信号を生成し各部分に送信するシステム動作制御部21Aの他に、判定部21B及び光量変更部21Cを備える。
FIG. 7 is a diagram for explaining the configuration of the system controller 21 of the processor 200.
As shown in FIG. 7, the system controller (control unit) 21 generates a control signal for controlling and managing the operation of each part of the electronic endoscope system 1 and transmits it to each part, in addition to the system operation control unit 21A A determination unit 21B and a light amount change unit 21C are provided.
 判定部21Bは、固体撮像素子14で所定の時間間隔で繰り返し撮像された生体組織の撮像画像の画像色成分が、設定された判定条件を満足するか否かの判定を行う部分である。判定条件は、撮像画像の各画素における異なる画像色成分の値同士の比率を用いた条件である。具体的には、判定部21Bは、体腔内の生体組織とは別の体腔内物質の像を含む撮像画像、例えば血液の像が含まれている撮像画像について上記判定をするために、判定条件に用いる上記比率として、撮像画像の注目画像色成分の値に対する、注目画像色成分以外の画像色成分の値の比率を算出して判定を行う。ここで、撮像画像の注目画像色成分とは、固体撮像素子14の感度波長帯域の中で血液(体腔内物質)の光反射率が最も高い波長を含む撮像画像の画像色成分である。光反射率が最も高い波長を含む撮像画像の注目画像色成分とは、血液の場合、赤色の光成分を最もよく反射するので、注目画像色成分は、固体撮像素子14で撮像された画像の赤色の画像色成分である。 The determination unit 21B is a portion that determines whether or not the image color component of the captured image of the biological tissue repeatedly captured at predetermined time intervals by the solid-state imaging device 14 satisfies the set determination condition. The determination condition is a condition using a ratio of values of different image color components in each pixel of the captured image. Specifically, the determination unit 21B determines the determination condition in order to make the above determination on a captured image including an image of a substance in the body cavity different from the living tissue in the body cavity, for example, a captured image including an image of blood. The determination is performed by calculating the ratio of the values of image color components other than the target image color component to the value of the target image color component of the captured image as the above ratio used for. Here, the target image color component of the captured image is an image color component of the captured image including the wavelength at which the light reflectance of blood (subjacent substance) is the highest in the sensitivity wavelength band of the solid-state imaging device 14. The target image color component of the captured image including the wavelength with the highest light reflectance is the red light component most reflected in the case of blood, so the target image color component is the image of the image captured by the solid-state imaging device 14 It is a red image color component.
 図8は、固体撮像素子14の各受光位置の前面に設けられる原色色フィルタの透過率のスペクトル波形の一例を示す図である。図8に示す色フィルタの透過率のスペクトル波形において、透過率が0より大きい波長帯域が、固体撮像素子14における感度波長帯域である。このように、判定部21Bは、撮像画像の注目画像色成分の値と、それ以外の画像色成分の値の比率を算出する。この場合、注目画像色成分は、図8に示すRで示された波長帯域の赤色の色成分Rである。したがって、青色の色成分の値をDbとし、緑色の色成分の値をDgとし、注目画像色成分である赤色の色成分の値をDrとしたとき、判定部21Bで算出する比率は、Db/Drあるいは、Dg/Drである。このように、同じ画素中の画像色成分の比率を用いるのは、画素毎に異なる輝度の影響をなくすためである。したがって、Db/Drあるいは、Dg/Drに代えて、同じ画素におけるDrと輝度成分の値の比率を用いることもできる。
 このような比率を用いて、撮像画像の画像色成分が判定条件を満足するか否かを判定部21Bは判定する。判定条件は、例えば、撮像画像内に、Db/DrあるいはDg/Drの値が閾値以下となる画素数が多い場合、すなわち、撮像画像中に血液の像が多い場合、被写体である生体組織上に血液が流出して、照明窓12に血液が付着した可能性が高い、と判定するための条件である。このような判定条件については後述する。
FIG. 8 is a diagram showing an example of a spectral waveform of the transmittance of the primary color filter provided on the front surface of each light receiving position of the solid-state imaging device 14. In the spectral waveform of the transmittance of the color filter shown in FIG. 8, the wavelength band where the transmittance is greater than 0 is the sensitivity wavelength band in the solid-state imaging device 14. Thus, the determination unit 21B calculates the ratio of the value of the target image color component of the captured image to the value of the other image color components. In this case, the target image color component is the red color component R of the wavelength band indicated by R shown in FIG. Therefore, assuming that the value of the blue color component is Db, the value of the green color component is Dg, and the value of the red color component that is the target image color component is Dr, the ratio calculated by the determination unit 21B is Db / Dr or Dg / Dr. Thus, the reason for using the ratio of image color components in the same pixel is to eliminate the influence of the luminance which is different for each pixel. Therefore, instead of Db / Dr or Dg / Dr, it is also possible to use the ratio of the value of Dr to the luminance component in the same pixel.
Using such a ratio, the determination unit 21B determines whether the image color component of the captured image satisfies the determination condition. The determination condition is, for example, when there are a large number of pixels for which the value of Db / Dr or Dg / Dr is equal to or less than the threshold in the captured image, that is, when there are many images of blood in the captured image It is a condition for determining that blood is likely to have flowed out and the blood has adhered to the illumination window 12. Such determination conditions will be described later.
 光量変更部21Cは、判定部21Bにおける判定の結果に応じて、光源装置300が出射する複数の光のうち一部の光の単位時間当たりの光量を変更する、例えば光量を低減するように光源装置300を制御する。一実施形態では、光強度を低下することで光の単位時間当たりの光量を低下させる。別の一実施形態では、光量を低下させる場合、光強度を一定にしたまま、固体撮像素子14が光電変換による撮像を行っている期間を外して、光の出射を一定の期間連続的にあるいは断続的にオフにすることにより、光の単位時間当たりの光量を変更する(低下させる)。具体的には、光量変更部21Cは、体腔内物質の吸光が低減するように、体腔内物質の吸光率に応じて定められる照明光の光成分を光量制御対象光として光量を変更する。より具体的には、光量変更部21Cは、光源装置300が出射する光の中で、血液の吸光率が所定の値よりも高い光、例えば最も高い光を光量制御対象光として、光量制御対象光の光量を変更するように光源駆動回路340の動作を制御する。
 図9は、血液の吸光率のスペクトル波形を示す図である。図9に示すように、410~420nmの範囲、特に415nmで血液の吸光率が最大になる。このため、光強度を低下する光量制御対象光は、光源ユニット315が出射する紫色の光Lvとなる。
The light amount changing unit 21C changes the light amount per unit time of some of the plurality of lights emitted by the light source device 300 according to the determination result of the determining unit 21B, for example, a light source to reduce the light amount. The device 300 is controlled. In one embodiment, reducing the light intensity reduces the amount of light per unit time. In another embodiment, when the light intensity is reduced, the period during which the solid-state imaging device 14 performs imaging by photoelectric conversion is removed while the light intensity is kept constant, or the light emission is continuously performed for a certain period or By switching off intermittently, the amount of light per unit time is changed (decreased). Specifically, the light quantity changing unit 21C changes the light quantity by using the light component of the illumination light determined according to the absorptivity of the substance in the body cavity as the light quantity control target light so that the light absorption of the substance in the body cavity is reduced. More specifically, the light quantity change unit 21C sets the light quantity control target as the light quantity control target light whose light absorptivity of blood is higher than a predetermined value, for example, the highest light among the lights emitted by the light source device 300. The operation of the light source drive circuit 340 is controlled to change the amount of light.
FIG. 9 is a diagram showing a spectral waveform of blood absorptivity. As shown in FIG. 9, the absorptivity of blood is maximized in the range of 410 to 420 nm, particularly at 415 nm. For this reason, the light amount control target light whose light intensity is reduced becomes purple light Lv emitted from the light source unit 315.
 このように、判定部21Bにより判定した結果に応じて、光量変更部21Cは、体腔内物質の吸光が低減するように、体腔内物質の吸光率に応じて定められる照明光の光成分を光量制御対象光として光量を変更する。また、一実施に形態によれば、光量変更部21Cは、光量制御対象光として照明光Lのうち光量を低減する第1光成分と、光量を低減しない第2光成分とに分けて前記第1光成分の光量を低減するように構成される。この場合、第1光成分を吸光する体腔内物質の吸光率は、第2光成分を吸光する体腔内物質の吸光率より大きい、ことが好ましい。
 また、一実施形態によれば、光量制御対象光は、例えば、体腔内物質の吸光率が所定値よりも高い光成分であることが好ましく、より好ましくは、吸光率が最大となる光成分である。言い換えると、光量制御対象光の波長は、体腔内物質の吸光率が最大となる波長を含むことが好ましい。
Thus, according to the result determined by the determination unit 21B, the light amount changing unit 21C converts the light component of the illumination light determined according to the absorptivity of the body cavity substance so that the light absorption of the body cavity substance is reduced. The light quantity is changed as the control target light. Further, according to one embodiment, the light amount changing unit 21C divides the illumination light L into a first light component for reducing the light amount and a second light component not for reducing the light amount as the light amount control target light. It is configured to reduce the amount of light of one light component. In this case, it is preferable that the absorptivity of the body cavity material that absorbs the first light component is larger than the absorptivity of the body cavity material that absorbs the second light component.
Further, according to one embodiment, the light quantity control target light is, for example, a light component in which the absorptivity of the substance in the body cavity is higher than a predetermined value, and more preferably a light component having the maximum absorptivity. is there. In other words, it is preferable that the wavelength of light subject to light quantity control includes a wavelength at which the absorptivity of the substance in the body cavity is maximum.
 光量制御対象光の光強度は、例えば、図5に示す点線のように、擬似白色光における紫色の光Lvの光強度のレベルまで低下させなくてもよく、また、図6に示す擬似白色光における紫色の光Lvの光強度まで低下させてもよい。
 なお、光量変更部21Cは、光強度の低下に代えて、照明光全体の光量に対する光量制御対象光の光量の相対比の低下を行ってもよい。
The light intensity of the light quantity control target light does not have to be reduced to the level of the light intensity of the purple light Lv in the pseudo white light as indicated by the dotted line in FIG. 5, for example. It may be reduced to the light intensity of the purple light Lv at.
Note that the light amount changing unit 21C may reduce the relative ratio of the light amount of the light amount control target light to the light amount of the entire illumination light, instead of reducing the light intensity.
 判定部21Bが、照明窓12に血液が付着した可能性が高いと判定する判定条件は、一実施形態によれば、撮像画像において、上述の比率Db/Drあるいは、Dg/Drが所定の閾値より小さい画素数が、許容限界値として予め定めた数より大きいか否かの条件Aを含むことが好ましい。撮像画像において、上記比率が所定の閾値より小さい画素数、例えば血液の像の画素数が多い場合、照明窓12に血液が付着した可能性が高いといえる。このような血液の像の画素数の上記許容限界値として、撮像画像の全画素に占める血液の像の画素の数の、予め定めた許容占有率の上限と、撮像画像の全画素の数とを乗算したものを用いてもよいし、撮像画像中の中心位置付近の特定の領域(例えば、撮像画像の画像サイズよりも小さく、撮像画像の中心位置を含む矩形または円形の領域)内の画素の数と、この特定の領域に占める血液の像の画素の数の、予め定めた許容占有率の上限とを乗算したものを用いてもよい。 According to one embodiment, the determination unit 21B determines that the possibility of blood adhering to the illumination window 12 is high, according to one embodiment, in the captured image, the above-mentioned ratio Db / Dr or Dg / Dr is a predetermined threshold value. It is preferable to include the condition A whether or not the smaller number of pixels is larger than a predetermined number as the allowable limit value. In the captured image, when the ratio is smaller than a predetermined threshold, for example, when the number of pixels of the image of blood is large, it can be said that blood is likely to be attached to the illumination window 12. As the above-mentioned allowable limit value of the number of pixels of the image of blood, the upper limit of the predetermined allowable occupancy rate of the number of pixels of the image of blood occupied in all pixels of the captured image, and the number of all pixels of the captured image The pixel in the specific area (for example, a rectangular or circular area smaller than the image size of the captured image and including the central position of the captured image) in the captured image may be used. .Times..times..times..times..times..times..times..times..times..times..times..times..times..times..times.
 また、一実施形態によれば、判定条件は、時系列で得られた撮像画像において、上述の比率の時間変化が所定の範囲を超えて大きくなった画素数が、許容限界値として予め定めた数より大きいか否かの条件Bを含むことが好ましい。比率の時間変化とは、例えば、時系列で得られた動画の撮像画像のうち、撮像時間が隣り合う2つの撮像画像における上記比率を、2つの撮像画像の撮像時間の差で割ったものである。撮像画像において、血液が生体組織に流出した場合、上述の比率の時間変化(時間変化が負の場合、時間変化の絶対値をいう)が所定の範囲を超えて大きくなる(比率の変化が大きくなる)ので、このような画素数が多い場合、生体組織上に血液が流出したことを意味し、照明窓12に血液が付着した可能性が高いといえる。このように生体組織の像から血液の像に変化した画素数の上記許容限界値として、撮像画像の全画素に占める血液の像に変化する画素の数の、予め定めた許容占有率の上限と、撮像画像の全画素の数とを乗算したものを用いてもよいし、撮像画像中の中心位置付近の特定の領域(例えば、撮像画像の画像サイズよりも小さく、撮像画像の中心位置を含む矩形または円形の領域)内の画素の数と、この特定の領域に占める血液の像に変化する画素の数の、予め定めた許容占有率の上限とを乗算したものを用いてもよい。判定条件は、条件Aと条件Bを同時に含むことも好ましい。
 この場合、条件A、あるいは条件B、あるいは条件A及び条件Bにおける画素数が予め定めた数より大きい場合、光量変更部21Cは、光量制御対象光の光量を低くするように光源装置300を制御することも好ましい。
Further, according to one embodiment, in the captured image obtained in time series, the determination condition is predetermined as the allowable limit value of the number of pixels of which the temporal change of the above-mentioned ratio increases beyond a predetermined range. It is preferable to include the condition B which is larger than the number. The temporal change of the ratio is, for example, the ratio of the above-mentioned ratio in two captured images adjacent to each other among the captured images of moving images obtained in time series divided by the difference between the captured times of the two captured images. is there. In the captured image, when blood flows out to a living tissue, the time change of the above ratio (when the time change is negative, it means the absolute value of the time change) becomes larger than the predetermined range (the change of the ratio is large Therefore, when such a number of pixels is large, it means that blood has flowed out on the living tissue, and it can be said that there is a high possibility that the blood has adhered to the illumination window 12. The upper limit of the predetermined allowable occupancy rate of the number of pixels changing to the image of blood occupied in all the pixels of the captured image as the above-mentioned allowable limit value of the number of pixels changed from the image of living tissue to the image of blood in this way Alternatively, a product obtained by multiplying the number of all pixels of the captured image may be used, or a specific area near the center position in the captured image (for example, smaller than the image size of the captured image, including the center position of the captured image) The number of pixels in the rectangular or circular area) may be multiplied by the upper limit of the predetermined allowable occupancy rate of the number of pixels changing to the image of blood occupied in this specific area. It is also preferable that the determination conditions include condition A and condition B simultaneously.
In this case, when the number of pixels under condition A, condition B, or condition A and condition B is larger than a predetermined number, the light quantity changing unit 21C controls the light source device 300 to reduce the light quantity of light subject to light quantity control. Is also preferred.
 また、一実施形態によれば、判定条件は、時系列で得られた撮像画像において、上述の比率が所定の閾値より小さい画素数が、予め定めた数より大きい状態が続く継続時間が許容限界値として予め定めた時間より長いか否かの条件Cを含むことが好ましい。撮像画像において、比率が所定の閾値より小さい画素数が予め定めた時間継続して存在する、例えば、血液の像が予め定めた時間継続して存在する場合、照明窓12に血液が付着した可能性が高いといえる。 Further, according to one embodiment, the determination condition is that, in the captured image obtained in time series, the duration for which the number of pixels whose ratio is smaller than the predetermined threshold is larger than the predetermined number continues to be permitted. It is preferable to include the condition C as to whether the value is longer than a predetermined time. In the captured image, the number of pixels whose ratio is smaller than a predetermined threshold value is continuously present for a predetermined time, for example, when the image of blood is continuously present for a predetermined time, blood may be attached to the illumination window 12 It can be said that the sex is high.
 一実施形態によれば、判定条件は、時系列で得られた撮像画像において、上述の比率の時間変化が所定の範囲を超えて大きくなった画素数が、予め定めた数より大きい状態が続く継続時間が許容限界値として予め定めた時間より長いか否かの条件Dを含むことが好ましい。比率の時間変化が所定の範囲を超えて大きくなった画素数、例えば、生体組織の像から血液の像に急激に変化した画素数が予め定めた時間継続して存在する、例えば、血液の像が急激に増えて予め定めた時間継続して存在する場合、体腔内に血液が流出して照明窓12に血液が付着した可能性が高いといえる。 According to one embodiment, the determination condition is that, in the captured images obtained in time series, the state in which the number of pixels whose temporal change of the above-mentioned ratio increases beyond a predetermined range is larger than a predetermined number continues It is preferable to include the condition D whether the duration is longer than a predetermined time as an allowable limit value. The number of pixels in which the temporal change of the ratio is increased beyond a predetermined range, for example, the number of pixels which has been rapidly changed from an image of a living tissue to an image of blood continuously exists for a predetermined time. Is rapidly increasing and continuously existing for a predetermined time, it is highly likely that blood has flowed into the body cavity and blood has adhered to the illumination window 12.
 判定部21Bは、判定条件として上述の条件A~Dの少なくとも2つ以上の条件を組み合わせたものを用いて判定してもよい。
 一実施形態によれば、条件A、Bを満足し、かつ条件C,Dを満足する場合、光量制御部21Bは、光量制御対象光の光量を低くするように光源装置300を制御することが好ましい。
The determination unit 21B may make a determination using a combination of at least two of the above conditions A to D as the determination condition.
According to one embodiment, when the conditions A and B are satisfied and the conditions C and D are satisfied, the light quantity control unit 21B may control the light source device 300 to reduce the light quantity of the light quantity control target light. preferable.
 一実施形態によれば、光量変更部21Bは、光量制御対象光の単位時間当たりの光量を複数の光量レベルに分けて順次段階的に変更してもよい。この場合、例えば、光量制御対象光の光強度を複数の強度レベルに分けて順次段階的に変更する場合、判定部21Bは、光量制御対象光の変更後の光強度(光量)に応じて、判定条件で用いる、上述の条件A~Dの許容限界値、すなわち予め定めた数あるいは上述の予め定めた時間を変更するための参照テーブルを備えることが好ましい。参照テーブルは、光量制御対象光の光強度と、判定条件で用いる上述の許容限界値とを対応させて記憶した情報である。光量制御対象光の光強度を段階的に下げた場合、光量制御対象光の強度レベルが高いときに、許容限界値として用いる上述の予め定めた数あるいは上述の予め定めた時間は、光量制御対象光の強度レベルが低いときに用いる許容限界値と異なる。精度の高い判定をする点から、許容限界値は光量制御対象光の強度レベルに応じて変更することが好ましい。 According to one embodiment, the light quantity changing unit 21B may divide the light quantity per unit time of the light quantity control target light into a plurality of light quantity levels and sequentially change the light quantity in a stepwise manner. In this case, for example, when the light intensity of the light amount control target light is divided into a plurality of intensity levels and sequentially changed in stages, the determination unit 21B determines the light intensity (light amount) after the change of the light amount control target light. It is preferable to provide a reference table for changing the allowable limit values of the above-mentioned conditions A to D, that is, the predetermined number or the above-mentioned predetermined time, which is used in the judgment condition. The reference table is information in which the light intensity of the light amount control target light and the above-described allowable limit value used in the determination condition are stored in association with each other. When the light intensity of the light quantity control target light is lowered stepwise, when the intensity level of the light quantity control object light is high, the above predetermined number used as the allowable limit value or the above predetermined time is the light quantity control target Different from the tolerance limits used when the light intensity level is low. It is preferable to change the allowable limit value according to the intensity level of the light quantity control target light in order to make the determination with high accuracy.
 図10は、一実施形態のシステムコントローラ21の構成の一例を示す図である。一実施形態によれば、電子スコープ100の操作部52は、送気送水ポート64から空気や水(流体)を吐出させるために空気や水を供給する流体送出機構70(例えば、シリンジポンプ等)と接続される。流体送出機構は、空気や水を供給する管を通して操作部52に接続されている。この場合、システムコントローラ21は、システム動作制御部21A、判定部21B、光量変更部21Cの他に、流体送出機構の動作の制御を行う流体動作制御部21Dを備えることが好ましい。光量変更部21Cが光量制御対象光の光量を変更する時に、流体動作制御部21Dは、流体送出機構70の動作の制御を行うことが、早期に付着した血液を取り除く点から好ましい。 FIG. 10 is a diagram illustrating an example of the configuration of the system controller 21 according to an embodiment. According to one embodiment, the operation unit 52 of the electronic scope 100 is a fluid delivery mechanism 70 (for example, a syringe pump or the like) that supplies air or water to discharge air or water (fluid) from the air / water supply port 64. Connected with The fluid delivery mechanism is connected to the operation unit 52 through a pipe for supplying air or water. In this case, in addition to the system operation control unit 21A, the determination unit 21B, and the light quantity change unit 21C, the system controller 21 preferably includes a fluid operation control unit 21D that controls the operation of the fluid delivery mechanism. When the light quantity changing unit 21C changes the light quantity of the light quantity control target light, it is preferable that the fluid operation control unit 21D perform the control of the operation of the fluid delivery mechanism 70 from the point of removing blood adhering early.
 図11は、さらに他の一実施形態のシステムコントローラ21の構成の一例を示す図である。一実施形態によれば、システムコントローラ(制御部)21は、システム動作制御部21A、判定部21B、光量変更部21Cの他に、撮像画像の輝度成分の平均値の低下に応じて、光源装置300が出射する照明光全体の光量が増加するように(光量が波長帯域全体で一律に増加するように)光源装置300の光源駆動回路340を制御する自動光量調整部21Eを備えてもよい。自動光量調整部21Eは、通常、被写体である生体組織と先端面57との間の距離(撮像距離)の長短によって撮像画像の輝度が変動することを抑えるために用いられる。しかし、自動光量調整部21Eは、判定部21Bにおける判定の際にも有効に用いることができる。すなわち、判定部21Bは、上記判定条件を用いた判定に加えて、さらに、増加した照明光全体の光量(単位時間当たりの光量)が予め定めた量を超えたか否かを判定し、増加した照明光全体の光量が予め定めた量を超えた場合に、光量制御対象光の光量を変更するように光源装置300を制御することが好ましい。血液が照明窓12に付着した場合、照明光Lの一部を吸収して照明光が急激に暗くなるので、自動光量調整部21Eは、照明光の明るさが一定となるように光量を増加する。しかし、この自動光量調整部21Eが照明光の光量を上げても、撮像画像の輝度成分の平均値の向上が十分でなく、依然として平均値が小さい場合、照明窓12に血液が付着した可能性が高い。この場合、照明光全体の光量は、通常に比べて大きくなる。したがって、上述の判定条件を満足し、かつ照明光における増加した照明光全体の光量が予め定めた量、例えば、血液が照明窓12に付着していない場合に上昇する光量の上限を超えた場合に、光量制御対象光の光量を変更するように光源装置300を制御することが、照明窓12に血液が付着したことをより確実に判定して、血液が照明窓12へ固着することを抑制することができる点から好ましい。
 自動光量調整部21Eは、光源装置300の射出する現在の照明光Lの光量の情報を、自動光量調整部21Eが光源駆動回路340に送る制御信号から取得することができる。
 さらに、他の一実施形態では、図11に示すシステムコントローラ21に、図10に示す流体動作制御部21Dを設けてもよい。この場合、判定部21Bが、照明光における増加した照明光全体の光量が予め定めた量を超えたか否かを判定する前に、流体動作制御部21Dが送気送水ポート64から空気や水(流体)を吐出させる動作の制御を行うことが好ましい。判定部21Bにおける照明光の光量の判定の前に照明窓12を洗浄するので、洗浄した照明窓12を判定の対象とすることができる。
FIG. 11 is a diagram showing an example of the configuration of a system controller 21 according to still another embodiment. According to one embodiment, in addition to the system operation control unit 21A, the determination unit 21B, and the light amount change unit 21C, the system controller (control unit) 21 determines the light source device according to the decrease in the average value of the luminance components of the captured image. The automatic light amount adjustment unit 21E may be provided to control the light source drive circuit 340 of the light source device 300 such that the light amount of the entire illumination light emitted by the light source 300 increases (so that the light amount increases uniformly in the entire wavelength band). The automatic light quantity adjustment unit 21E is generally used to suppress fluctuations in the luminance of a captured image due to the length (short distance) of the distance (imaging distance) between the living tissue as the subject and the distal end surface 57. However, the automatic light amount adjustment unit 21E can be effectively used also in the determination by the determination unit 21B. That is, in addition to the determination using the determination condition, the determination unit 21B further determines whether the increased light amount of the entire illumination light (light amount per unit time) exceeds a predetermined amount. It is preferable to control the light source device 300 so as to change the light quantity of the light quantity control target light when the light quantity of the entire illumination light exceeds a predetermined quantity. When blood adheres to the illumination window 12, it absorbs part of the illumination light L and the illumination light becomes dark rapidly, so the automatic light amount adjustment unit 21E increases the light amount so that the brightness of the illumination light becomes constant. Do. However, even if the automatic light quantity adjustment unit 21E increases the light quantity of the illumination light, the improvement of the average value of the luminance components of the captured image is not sufficient, and if the average value is still small, the possibility of blood adhering to the illumination window 12 Is high. In this case, the light quantity of the entire illumination light is larger than usual. Therefore, when the above-described determination condition is satisfied, and the light amount of the increased total illumination light in the illumination light exceeds a predetermined amount, for example, the upper limit of the light amount that increases when blood is not attached to the illumination window 12 In addition, controlling the light source device 300 to change the light amount of the light amount control target light more reliably determines that the blood adheres to the illumination window 12 and suppresses the blood from adhering to the illumination window 12 It is preferable from the point which can be done.
The automatic light quantity adjustment unit 21E can acquire information on the light quantity of the present illumination light L emitted from the light source device 300 from the control signal that the automatic light quantity adjustment unit 21E sends to the light source drive circuit 340.
Furthermore, in another embodiment, the system controller 21 shown in FIG. 11 may be provided with a fluid operation control unit 21D shown in FIG. In this case, before the determination unit 21B determines whether the light amount of the increased total illumination light in the illumination light exceeds a predetermined amount, the fluid operation control unit 21D receives air or water from the air / water supply port 64 ( It is preferable to control the operation of discharging the fluid. Since the illumination window 12 is cleaned before the determination of the light amount of the illumination light in the determination unit 21B, the cleaned illumination window 12 can be used as the determination target.
 図2に示すように、プロセッサ200は、撮像画像を画像処理する前段処理回路26(画像処理部)を備える。前段処理回路26は、撮像画像の画像信号のゲイン調整を行う。この場合、前段処理回路26は、光量制御対象光の光量の変更後に固体撮像素子14で撮像した撮像画像中の、光量制御対象光の波長帯域を含む波長帯域の画像色成分、すなわち、注目画像色成分に対するゲイン調整量を光量制御対象光の光量の変化量に応じて変更することが好ましい。上述の例では、光量制御対象光は紫色の光Lvであり、この紫色の光Lvは、図8に示すように、青色(B)の波長帯域に含まれるので、青色の画像色成分のゲインを、紫色の光Lvの光量の変化量に応じて変更する。具体的には、紫色の光Lvの光量を低くする場合、紫色の光Lvの光量を低くするほど、青色の画像色成分の値を増加するためのゲインを高くする。
 これにより、光量制御対象光の光量を低下させた場合でも、モニタ400に表示される撮像画像の色バランスは、光量の変更の前後で維持され、術者は、生体組織の撮像画像をストレス無く観察することができる。
As shown in FIG. 2, the processor 200 includes a pre-processing circuit 26 (image processing unit) that performs image processing on a captured image. The pre-processing circuit 26 adjusts the gain of the image signal of the captured image. In this case, the pre-processing circuit 26 generates an image color component of a wavelength band including the wavelength band of the light amount control target light in the captured image captured by the solid-state imaging device 14 after changing the light amount of the light amount control target light It is preferable to change the gain adjustment amount for the color component in accordance with the change amount of the light quantity of the light quantity control target light. In the above-mentioned example, the light quantity control target light is purple light Lv, and this purple light Lv is included in the blue (B) wavelength band as shown in FIG. , According to the amount of change of the light quantity of the purple light Lv. Specifically, when the light amount of the purple light Lv is reduced, the gain for increasing the value of the blue image color component is increased as the light amount of the purple light Lv is decreased.
Thereby, even when the light amount of the light to be controlled is reduced, the color balance of the captured image displayed on the monitor 400 is maintained before and after the change of the light amount, and the operator does not stress the captured image of the living tissue. It can be observed.
 一実施形態によれば、図5、8に示すように、青色(B)の波長帯域には、光源ユニット314から出射される青色の光Lbの波長帯域も含まれる。このため、紫色の光Lvの光量を低下させた場合、青色の光Lbの光量を増加させて、光量の変化前後の、モニタ400に表示される撮像画像の色バランスを維持することも好ましい。すなわち、撮像画像の画像色成分の1つである画像色成分A(例えば、青色の画像色成分)は、光源装置300から出射する複数の光のうち、光量制御対象光(例えば、紫色の光Lv)の波長帯域の他に、少なくとも1つの別の光(例えば、青色の光Lb)の波長帯域を画像色成分Aの波長帯域として含む。このとき、光量変更部21Cは、光量制御対象光(例えば、紫色の光Lv)の光量を変更した(例えば低下させた)とき、画像色成分A(青色の画像色成分)の値の変化を抑制するために、別の光(例えば、青色の光Lb)の単位時間当たりの光量を変更する(増加させる)、ことが好ましい。このような実施形態は、上述のゲイン調整量の変更と組み合わせて行ってもよい。これにより、光量制御対象光の光量を低下させた場合でも、モニタ400に表示される撮像画像の色バランスは、光量の変更の前後で維持され、術者は生体組織の撮像画像をストレス無く観察することができる。 According to one embodiment, as shown in FIGS. 5 and 8, the wavelength band of blue (B) also includes the wavelength band of blue light Lb emitted from the light source unit 314. Therefore, when the light amount of the purple light Lv is decreased, it is also preferable to increase the light amount of the blue light Lb and maintain the color balance of the captured image displayed on the monitor 400 before and after the change of the light amount. That is, an image color component A (for example, a blue image color component) which is one of the image color components of the captured image is a light quantity control target light (for example, violet light) among a plurality of lights emitted from the light source device 300 In addition to the wavelength band of Lv), the wavelength band of at least one other light (for example, blue light Lb) is included as the wavelength band of the image color component A. At this time, when the light quantity changing unit 21C changes (for example, reduces) the light quantity of the light quantity control target light (for example, purple light Lv), the change of the value of the image color component A (blue image color component) In order to suppress, it is preferable to change (increase) the light amount per unit time of another light (for example, blue light Lb). Such an embodiment may be performed in combination with the above-described change in gain adjustment amount. Thereby, even when the light amount of the light to be controlled is reduced, the color balance of the captured image displayed on the monitor 400 is maintained before and after the change of the light amount, and the operator observes the captured image of the living tissue without stress. can do.
 また、システムコントローラ21(制御部)は、撮像画像の画像色成分が判定条件を満足する場合、照明光を生体組織に向けて照明する照明窓12に血液が付着した可能性がある旨の情報を報知するために、図11に示すように、モニタ400に上記情報を送信する報知制御部21Fを備えることも好ましい。これにより、術者は、照明窓12の洗浄をマニュアルで早期に行うことができる。このため、照明窓12に血液が固着することを抑制することができる。また、報知制御部21Fは、特殊観察モードによる体腔内の観察を続行して行える旨の情報をモニタ400が報知させるように送信することも好ましい。
 この場合、照明窓12に血液が付着した可能性がある旨の情報の報知から所定時間が経過した後、例えば、10秒経過後、光量変更部21Cは、光量制御対象光の光量の変更を行うことが好ましい。術者に対して情報を送信して事前に報知することで、術者は撮像画像の色変化が生じるかもしれない心構えができ、安定した観察、診断、あるいは処置を続けることができる。
 照明窓12の洗浄により、血液が取り除かれた場合、例えば、撮像画像の輝度成分の平均値が回復した場合、光量制御対象光の光強度を元の光強度に戻してもよい。
In addition, when the image color component of the captured image satisfies the determination condition, the system controller 21 (control unit) information that blood may be attached to the illumination window 12 for illuminating the illumination light toward the living tissue. It is also preferable to include a notification control unit 21F that transmits the above information to the monitor 400, as shown in FIG. Thus, the operator can manually clean the illumination window 12 at an early stage. For this reason, it can suppress that blood adheres to the illumination window 12. Furthermore, it is preferable that the notification control unit 21F transmit information so that the monitor 400 can notify that the observation in the body cavity in the special observation mode can be continued.
In this case, after a predetermined time has elapsed from notification of information indicating that blood may be attached to the illumination window 12, for example, after 10 seconds, the light quantity change unit 21C changes the light quantity of the light quantity control target light It is preferred to do. By transmitting information to the operator and notifying in advance, the operator can prepare for the possibility of color change of the captured image, and can continue stable observation, diagnosis or treatment.
When blood is removed by cleaning the illumination window 12, for example, when the average value of the luminance components of the captured image is recovered, the light intensity of the light quantity control target light may be returned to the original light intensity.
 上述の実施形態では、体腔内物質として、体腔内に流出した血液を対象に説明したが、体腔内物質は、生体組織から分泌する生体物質、及び生体外から体腔内に導入され体腔内に残る外部物質(食物)の残渣等の体腔内物質を含む。この場合、光量制御対象光は紫色の光に限定されず、体腔内物質の吸光率に応じて変わる。また、体腔内物質の反射特性に応じて、判定条件に用いる撮像画像の注目画像色成分の種類も変わる。
 なお、光量変更部21Cは、上述したように、判定部21Bにより判定した結果に応じて、体腔内物質の吸光が低減するように、体腔内物質の吸光率に応じて照明光の少なくとも1つの光成分を光量制御対象光として光量を変更するように構成される。具体的には、体腔内物質の吸光率の高い光の光量が低下するように構成される。しかし、光量制御対象光は、吸光率が低い光の光量を大きくしてもよい。
In the above-described embodiment, the body cavity material is described for blood that has flowed into the body cavity, but the body cavity material is a biological material that is secreted from living tissue and is introduced from outside the body into the body cavity and remains in the body cavity. It contains substances in the body cavity such as residues of external substances (food). In this case, the light quantity control target light is not limited to purple light and changes according to the absorptivity of the substance in the body cavity. In addition, the type of the target image color component of the captured image used for the determination condition also changes according to the reflection characteristic of the substance in the body cavity.
Note that, as described above, the light amount changing unit 21C causes at least one of the illumination light to be reduced according to the absorptivity of the body cavity material so that the light absorption of the body cavity material is reduced according to the result determined by the determining unit 21B. The light component is configured to change the light quantity as the light quantity control target light. Specifically, the light quantity of light having a high absorptivity of the substance in the body cavity is configured to be reduced. However, the light quantity control target light may increase the light quantity of light having a low absorptivity.
 以上、本発明の電子内視鏡システムについて詳細に説明したが、本発明の電子内視鏡システムは上記実施形態に限定されず、本発明の主旨を逸脱しない範囲において、種々の改良や変更をしてもよいのはもちろんである。 As mentioned above, although the electronic endoscope system of the present invention was explained in detail, the electronic endoscope system of the present invention is not limited to the above-mentioned embodiment, In the range which does not deviate from the main point of the present invention, various improvement or change Of course it is good.
1 電子内視鏡システム
11 LCB(Light Carrying Bundle)
12 照明窓
13 観察窓
14 固体撮像素子
15 ドライバ信号処理回路
21 システムコントローラ
21A システム動作制御部
21B 判定部
21C 光量変更部
21D 流体動作制御部
21E 自動光量調整部
21F 報知制御部
22 タイミングコントローラ
23,16 メモリ
24 操作パネル
26 前段信号処理回路
27 画像メモリ
28 後段信号処理回路
50 コネクタ部
51 ケーブル
52 操作部
54 挿入部
56 先端部
57 先端面
58 可撓管
60 屈曲部
62 処置具用開口
64 送気送水ポート
70 流体送出機構
100 電子スコープ
200 プロセッサ
300 光源装置
310 光源部
312,313,314,315 光源ユニット
322,323,324,325 コリメートレンズ
333,334,335 光学素子
340 光源駆動回路
350 集光レンズ
1 Electronic Endoscope System 11 LCB (Light Carrying Bundle)
12 illumination window 13 observation window 14 solid-state imaging device 15 driver signal processing circuit 21 system controller 21A system operation control unit 21B determination unit 21C light amount change unit 21D fluid operation control unit 21E automatic light amount adjustment unit 21F notification control unit 22 timing controller 23, 16 Memory 24 Operation panel 26 Pre-stage signal processing circuit 27 Image memory 28 Post-stage signal processing circuit 50 Connector part 51 Cable 52 Operation part 54 Insertion part 56 Tip part 57 Tip surface 58 Flexible tube 60 Bend part 62 Treatment tool opening 64 Air supply water Port 70 Fluid delivery mechanism 100 Electronic scope 200 Processor 300 Light source device 310 Light source units 312, 313, 314, 315 Light source units 322, 323, 324, 325 Collimating lenses 333, 334, 335 Optical element 340 Light source drive circuit 350 collection Light lens

Claims (17)

  1.  体腔内の生体組織を撮像するように構成された電子内視鏡及びプロセッサを備える電子内視鏡システムであって、
     照明光を出射するように構成された光源部と、
     前記電子内視鏡に設けられ、前記照明光で照明された前記生体組織を撮像するように構成された撮像素子と、
     前記プロセッサに設けられ、前記撮像素子で撮像された前記生体組織の撮像画像が、前記撮像画像の画素における異なる画像色成分の値同士の比率を用いた判定条件を満足するか否かの判定を行うように構成された判定部と、前記判定の結果に応じて、前記照明光が含む光成分のうち一部の光成分の単位時間当たりの光量を変更するように前記光源部を制御するように構成された光量変更部と、を備える制御部と、を備え、
     前記判定は、前記撮像素子で撮像された撮像画像が、体腔内の前記生体組織とは別の体腔内物質の像を含む撮像画像であるか否かを前記比率によって行う判定であり、
     前記判定条件に用いる前記比率は、前記撮像素子の感度波長帯域の中で前記体腔内物質の光反射率が最も高い波長を含む前記撮像画像の注目画像色成分の値に対する、前記注目画像色成分以外の画像色成分の値の比率であり、
     前記光量変更部は、前記体腔内物質の吸光率に応じて定められる前記照明光の光成分を光量制御対象光として前記光成分の光量を変更するように構成されている、ことを特徴とする電子内視鏡システム。
    An electronic endoscope system comprising an electronic endoscope and a processor configured to image living tissue in a body cavity, the electronic endoscope system comprising:
    A light source configured to emit illumination light;
    An imaging device provided in the electronic endoscope and configured to image the living tissue illuminated by the illumination light;
    It is provided in the processor, and it is determined whether a captured image of the living tissue captured by the imaging device satisfies a determination condition using a ratio of values of different image color components in pixels of the captured image. The light source unit is controlled to change a light amount per unit time of a light component of a part of the light components included in the illumination light according to a determination unit configured to perform and a result of the determination. A control unit including the light amount change unit configured in
    The determination is determination based on the ratio as to whether or not the captured image captured by the imaging element is a captured image including an image of a body cavity material different from the living tissue in the body cavity.
    The ratio used for the determination condition is the image color component of interest with respect to the value of the image color component of interest of the captured image including the wavelength at which the light reflectance of the body cavity material is highest in the sensitivity wavelength band of the imaging element. It is a ratio of values of image color components other than
    The light amount changing unit is configured to change the light amount of the light component, with the light component of the illumination light determined according to the absorptivity of the substance in the body cavity as a light amount control target light. Electronic endoscope system.
  2.  前記照明光は、複数の光を前記光成分として合成した合成光であり、
     前記光量変更部は、前記光量制御対象光として前記照明光のうち光量を低減する第1光成分と、光量を低減しない第2光成分とに分けて前記第1光成分の光量を低減するように構成され、前記第1光成分を吸光する前記体腔内物質の前記吸光率は、前記第2光成分を吸光する前記体腔内物質の前記吸光率より大きい、請求項1に記載の電子内視鏡システム。
    The illumination light is combined light obtained by combining a plurality of lights as the light component,
    The light amount changing unit is configured to reduce the light amount of the first light component by dividing it into a first light component for reducing the light amount among the illumination light as the light amount control target light and a second light component for which the light amount is not reduced. The electronic endoscopy according to claim 1, wherein the absorptivity of the body cavity substance configured to absorb the first light component is greater than the absorptivity of the body cavity substance absorbing the second light component. Mirror system.
  3.  前記光量制御対象光の波長は、前記体腔内物質の前記吸光率が最大となる波長を含む、請求項1または2に記載の電子内視鏡システム。
    The electronic endoscope system according to claim 1, wherein a wavelength of the light quantity control target light includes a wavelength at which the absorptivity of the substance in the body cavity is maximum.
  4.  前記判定条件は、前記撮像画像内において、前記比率が所定の閾値より小さい画素数が、許容限界値として予め定めた数より大きいか否かの条件を含む、請求項1~3のいずれか1項に記載の電子内視鏡システム。 The method according to any one of claims 1 to 3, wherein the determination condition includes a condition as to whether or not the number of pixels whose ratio is smaller than a predetermined threshold value is larger than a predetermined number as an allowable limit value in the captured image. The electronic endoscope system according to the item.
  5.  前記撮像素子は、前記生体組織を時系列で撮像するように構成され、
     前記判定条件は、前記撮像画像において、前記比率の時間変化が所定の範囲を超えて大きくなった画素数が、許容限界値として予め定めた数より大きいか否かの条件を含む、請求項1~4のいずれか1項に記載の電子内視鏡システム。
    The imaging device is configured to image the biological tissue in time series;
    The determination condition includes a condition as to whether or not the number of pixels of the captured image where the temporal change of the ratio has increased beyond a predetermined range is larger than a predetermined number as an allowable limit value. The electronic endoscope system according to any one of to 4.
  6.  前記撮像素子は、前記生体組織を時系列で撮像するように構成され、
     前記判定条件は、前記撮像画像において、前記比率が所定の閾値より小さい画素数が、予め定めた数より大きい状態が続く継続時間が、許容限界値として予め定めた時間より長いか否かの条件を含む、請求項1~5のいずれか1項に記載の電子内視鏡システム。
    The imaging device is configured to image the biological tissue in time series;
    The determination condition is whether or not the duration in which the number of pixels whose ratio is smaller than a predetermined threshold value is larger than a predetermined number is longer than the predetermined time as the allowable limit value in the captured image. The electronic endoscope system according to any one of claims 1 to 5, which comprises
  7.  前記撮像素子は、前記生体組織を時系列で撮像するように構成され、
     前記判定条件は、前記撮像画像において、前記比率の時間変化が所定の範囲を超えて大きくなった画素数が、予め定めた数より大きい状態が続く継続時間が許容限界値として予め定めた時間より長いか否かの条件を含む、請求項1~6のいずれか1項に記載の電子内視鏡システム。
    The imaging device is configured to image the biological tissue in time series;
    The determination condition is that, in the captured image, the duration time in which the number of pixels whose temporal change of the ratio is increased beyond a predetermined range is larger than a predetermined number continues as an allowable limit value. The electronic endoscope system according to any one of claims 1 to 6, which includes a long or not long condition.
  8.  前記光量変更部は、前記光量制御対象光の光量を複数の光量レベルに分けて順次段階的に変更し、
     前記判定部は、前記光量制御対象光の変更後の光量に応じて、前記判定条件で用いる前記許容限界値を変更するために、前記光量と前記許容限界値とを対応させた参照テーブルを備える、請求項4~7のいずれか1項に記載の電子内視鏡システム。
    The light quantity changer divides the light quantity of the light quantity control target light into a plurality of light quantity levels and sequentially changes them in stages.
    The determination unit includes a reference table in which the light amount is associated with the allowable limit value in order to change the allowable limit value used in the determination condition according to the light amount after the change of the light amount control target light. The electronic endoscope system according to any one of claims 4 to 7.
  9.  前記判定条件を満足する場合、前記光量変更部は、前記照明光の全光量に対する前記光量制御対象光の光量の相対比を低くするように前記光源部を制御するように構成されている、請求項1~8のいずれか1項に記載の電子内視鏡システム。 When the determination condition is satisfied, the light amount changing unit is configured to control the light source unit so as to reduce a relative ratio of the light amount of the light amount control target light to the total light amount of the illumination light. Item 9. The electronic endoscope system according to any one of Items 1 to 8.
  10.  前記制御部は、前記撮像画像の輝度成分の平均値の低下に応じて、前記光源部が出射する前記照明光全体の光量が増加するように前記光源部を制御するように構成された自動光量調整部を備え、
     前記判定部は、さらに、前記自動光量調整部により増加した前記照明光全体の光量が予め定めた量を超えたか否かを判定するように構成され、
     前記光量変更部は、前記判定条件を満足し、かつ前記照明光全体の光量が予め定めた量を超えた場合に、前記光量制御対象光の光量を変更するように前記光源部を制御するように構成されている、請求項1~9のいずれか1項に記載の電子内視鏡システム。
    The control unit is configured to control the light source unit so as to increase the light amount of the entire illumination light emitted from the light source unit according to a decrease in an average value of luminance components of the captured image. Equipped with an adjustment unit,
    The determination unit is further configured to determine whether or not the light amount of the entire illumination light increased by the automatic light amount adjustment unit exceeds a predetermined amount.
    The light amount change unit controls the light source unit to change the light amount of the light amount control target light when the determination condition is satisfied and the light amount of the entire illumination light exceeds a predetermined amount. The electronic endoscope system according to any one of claims 1 to 9, which is configured as follows.
  11.  前記電子内視鏡は、前記照明光を前記生体組織に向けて照明するための照明窓、前記生体組織の像を取り込むための観察窓、及び、前記照明窓及び前記観察窓の表面に向けて流体が吐出するように構成された流体吐出ポートを備えた先端面を有し、
     前記電子内視鏡は、前記流体吐出ポートから前記流体を吐出させるために前記流体を供給するように構成された流体送出機構と接続され、
     前記制御部は、前記流体吐出ポートから前記流体を吐出させるように前記流体送出機構の動作の制御を行うように構成された流体動作制御部を備え、
     前記判定部は、前記自動光量調整部により増加した前記照明光全体の光量が予め定めた量を超えたか否かを判定する前に、前記流体動作制御部は、前記流体吐出ポートから前記流体を吐出させる動作の制御を行うように構成されている、請求項10に記載の電子内視鏡システム。
    The electronic endoscope includes an illumination window for illuminating the illumination light toward the living tissue, an observation window for capturing an image of the living tissue, and a surface of the illumination window and the observation window. Having a tip surface with a fluid discharge port configured to discharge fluid;
    The electronic endoscope is connected with a fluid delivery mechanism configured to supply the fluid to eject the fluid from the fluid ejection port;
    The control unit includes a fluid operation control unit configured to control the operation of the fluid delivery mechanism so as to discharge the fluid from the fluid discharge port;
    Before the determination unit determines whether the light amount of the entire illumination light increased by the automatic light amount adjustment unit exceeds a predetermined amount, the fluid operation control unit causes the fluid to be discharged from the fluid discharge port. 11. The electronic endoscope system according to claim 10, wherein the electronic endoscope system is configured to perform control of an ejection operation.
  12.  前記電子内視鏡は、前記照明光を前記生体組織に向けて照明するための照明窓、前記生体組織の像を取り込むための観察窓、及び、前記照明窓及び前記観察窓の表面に向けて流体が吐出するように構成された流体吐出ポートを備えた先端面を有し、
     前記電子内視鏡は、前記流体吐出ポートから前記流体を吐出させるために前記流体を供給するように構成された流体送出機構と接続され、
     前記制御部は、前記光量変更部が前記光量制御対象光の光量を変更する時に、前記流体吐出ポートから前記流体を吐出させるように前記流体送出機構の動作の制御を行うように構成された流体動作制御部を備える、請求項1~10のいずれか1項に記載の電子内視鏡システム。
    The electronic endoscope includes an illumination window for illuminating the illumination light toward the living tissue, an observation window for capturing an image of the living tissue, and a surface of the illumination window and the observation window. Having a tip surface with a fluid discharge port configured to discharge fluid;
    The electronic endoscope is connected with a fluid delivery mechanism configured to supply the fluid to eject the fluid from the fluid ejection port;
    The control unit is configured to control the operation of the fluid delivery mechanism so as to discharge the fluid from the fluid discharge port when the light amount changing unit changes the light amount of the light amount control target light The electronic endoscope system according to any one of claims 1 to 10, comprising an operation control unit.
  13.  前記制御部は、前記光量制御対象光の光強度を変更することにより、前記光量制御対象光の単位時間当たりの光量を変更するように構成されている、請求項1~12のいずれか1項に記載の電子内視鏡システム。 The controller according to any one of claims 1 to 12, wherein the control unit is configured to change the light amount per unit time of the light amount control target light by changing the light intensity of the light amount control target light. The electronic endoscope system according to claim 1.
  14.  前記プロセッサは、前記撮像画像を画像処理するように構成された画像処理部を備え、
     前記画像処理部は、前記光量制御対象光の光量の変更後に前記撮像素子で撮像した前記撮像画像中の、前記光量制御対象光の波長帯域を含む波長帯域の画像色成分に対するゲイン調整量を、前記光量制御対象光の光量の変化量に応じて変更するように構成されている、請求項1~13のいずれか1項に記載の電子内視鏡システム。
    The processor includes an image processing unit configured to perform image processing on the captured image;
    The image processing unit is configured to adjust a gain adjustment amount for an image color component of a wavelength band including the wavelength band of the light amount control target light in the captured image captured by the imaging device after changing the light amount of the light amount control target light. The electronic endoscope system according to any one of claims 1 to 13, wherein the electronic endoscope system is configured to change according to the amount of change of the light amount of the light to be controlled.
  15.  前記撮像画像の画像色成分の1つである画像色成分Aは、前記光源部から出射する複数の光のうち、前記光量制御対象光の波長帯域の他に、少なくとも1つの別の光の波長帯域を、前記画像色成分Aの波長帯域として含み、
     前記光量変更部は、前記光量制御対象光の光量を変更したとき、前記画像色成分Aの値の変化を抑制するために、前記別の光の単位時間当たりの光量を変更するように構成されている、請求項1~14に記載の電子内視鏡システム。
    The image color component A, which is one of the image color components of the captured image, is a wavelength of at least one other light in addition to the wavelength band of the light quantity control target light among the plurality of lights emitted from the light source unit A band is included as a wavelength band of the image color component A,
    The light quantity changing unit is configured to change the light quantity per unit time of the other light in order to suppress a change in the value of the image color component A when the light quantity of the light quantity control target light is changed. The electronic endoscope system according to any one of claims 1 to 14.
  16.  前記電子内視鏡システムは、前記プロセッサに接続された、前記撮像画像を表示するように構成されえたモニタを備え
     前記制御部は、前記撮像画像の前記画像色成分が前記判定条件を満足する場合、前記照明光を前記生体組織に向けて照明するための照明窓に前記体腔内物質が付着した可能性がある旨の情報を報知するために、前記モニタに前記情報を送信するように構成された報知制御部を備える、請求項1~15のいずれか1項に記載の電子内視鏡システム。
    The electronic endoscope system includes a monitor connected to the processor and configured to display the captured image. The control unit determines that the image color component of the captured image satisfies the determination condition. The monitor is configured to transmit the information to notify information indicating that the intracavitary substance may be attached to an illumination window for illuminating the illumination light toward the living tissue; The electronic endoscope system according to any one of claims 1 to 15, further comprising a notification control unit.
  17.  前記報知制御部による前記情報の報知から所定時間経過後、前記光量変更部は、前記光量制御対象光の光量の変更を行うように構成されている、請求項16に記載の電子内視鏡システム。 17. The electronic endoscope system according to claim 16, wherein the light amount change unit is configured to change the light amount of the light amount control target light after a predetermined time has elapsed from notification of the information by the notification control unit. .
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