WO2021255903A1 - Endoscope - Google Patents

Endoscope Download PDF

Info

Publication number
WO2021255903A1
WO2021255903A1 PCT/JP2020/023995 JP2020023995W WO2021255903A1 WO 2021255903 A1 WO2021255903 A1 WO 2021255903A1 JP 2020023995 W JP2020023995 W JP 2020023995W WO 2021255903 A1 WO2021255903 A1 WO 2021255903A1
Authority
WO
WIPO (PCT)
Prior art keywords
end side
channel tube
main body
endoscope
base end
Prior art date
Application number
PCT/JP2020/023995
Other languages
French (fr)
Japanese (ja)
Inventor
洋佑 磯部
Original Assignee
オリンパス株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by オリンパス株式会社 filed Critical オリンパス株式会社
Priority to PCT/JP2020/023995 priority Critical patent/WO2021255903A1/en
Publication of WO2021255903A1 publication Critical patent/WO2021255903A1/en

Links

Images

Classifications

    • 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
    • A61B1/012Instruments 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 characterised by internal passages or accessories therefor
    • A61B1/018Instruments 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 characterised by internal passages or accessories therefor for receiving instruments

Definitions

  • an endoscope has an insertion part inserted into a subject such as a patient to acquire image data in the subject by an imaging device and to perform treatment with a treatment tool or the like.
  • the insertion passage for the treatment tool through which the treatment tool is inserted is such that a resin channel tube is attached to the opening of the tip member of the endoscope insertion portion via a mouthpiece, and the channel tube is attached to the base end side of the mouthpiece.
  • the channel tube is prevented from falling off by covering it with resin or tying it with a thread.
  • Patent Document 1 a step is required in which the first region has a higher pressure-resistant crushing property than the second region formed on the proximal end side, and the first region has a higher pressure-resistant crushing property. It has a problem that it becomes difficult to connect to a pipe member.
  • the present invention has been made in view of the above, and an object of the present invention is to provide an endoscope having a simple structure and capable of preventing the sheath from being caught in the mouthpiece.
  • the endoscope according to the present invention has a distal end side and a proximal end side in the longitudinal direction of an insertion portion inserted into a subject and having a distal end member on the distal end side.
  • the channel tube through which the treatment tool is inserted and the channel tube are aligned with the proximal end side of the opening of the distal end member, the proximal end side is covered with the channel tube, and the treatment instrument is inserted together with the opening and the channel tube.
  • a mouthpiece having a through hole constituting a passage, a first main body portion arranged around the outer periphery of the mouthpiece covered with the channel tube, and a base portion protruding from the base end side of the mouthpiece in the longitudinal direction are arranged.
  • a tubular holding member having a second main body portion is provided, and the outer diameter of the channel tube extending toward the proximal end side is set on the inner circumference of the second main body portion of the holding member.
  • a protrusion is formed to press the channel tube so as to be smaller than the outer diameter of the channel tube in contact with the main body, and the base end side of the protrusion forms a tapered surface that guides the outer diameter of the channel tube to gradually expand.
  • an index indicating the mounting position with the mouthpiece is arranged on the outer surface of the holding member.
  • the holding member has a notch across the index.
  • the difference between the inner diameter of the first main body and the outer diameter of the base end side of the mouthpiece is twice the wall thickness of the channel tube in the natural state. It is as follows.
  • the mouthpiece has an abutting surface for contacting with the channel tube.
  • the maximum bending angle of the curved portion is 130 ° or more in the above invention.
  • the curved portion is configured by connecting a plurality of curved pieces, and the distance between the curved pieces arranged on the tip end side is that of the curved piece arranged on the proximal end side. Less than the interval.
  • an endoscope having a simple configuration and capable of preventing the sheath having a built-in treatment tool from being caught in the mouthpiece.
  • FIG. 1 is a diagram schematically showing an endoscope system according to an embodiment of the present invention.
  • FIG. 2 is a perspective view schematically showing the tip configuration of the insertion portion of the ultrasonic endoscope according to the embodiment of the present invention.
  • FIG. 3 is a cross-sectional view of the ultrasonic endoscope of FIG.
  • FIG. 4 is an enlarged view of A in FIG.
  • FIG. 5 is a cross-sectional view of FIG. 4 in a state where the holding member is removed.
  • FIG. 6 is a cross-sectional view of an ultrasonic endoscope that does not correspond to the embodiment of the present invention.
  • FIG. 7 is a diagram illustrating the curvature of the curved portion of the endoscope of FIG. FIG.
  • FIG. 8 is a top view illustrating a modification 1 of the endoscope according to the embodiment of the present invention.
  • FIG. 9 is a cross-sectional view of FIG.
  • FIG. 10 is a top view of the endoscope according to the second modification of the present embodiment.
  • FIG. 11 is a top view of the endoscope according to the third modification of the present embodiment.
  • FIG. 12 is a top view of the endoscope according to the modified example 4 of the present embodiment.
  • FIG. 13 is a cross-sectional view illustrating the curvature of the endoscope according to the prior art.
  • FIG. 14 is a cross-sectional view illustrating the curvature of the endoscope according to the prior art.
  • FIG. 1 is a diagram schematically showing an endoscope system 1 according to an embodiment of the present invention.
  • the endoscope system 1 is a system for performing ultrasonic diagnosis in a subject such as a cavity of a living body using an ultrasonic endoscope.
  • the endoscope system 1 includes an ultrasonic endoscope 2, an ultrasonic observation device 3, an endoscope observation device 4, a display device 5, and a light source device 6.
  • the ultrasonic endoscope 2 converts an electrical pulse signal received from the ultrasonic observation device 3 into an ultrasonic pulse (acoustic pulse) by an ultrasonic vibrator provided at the tip thereof and irradiates the subject. At the same time, the ultrasonic echo reflected by the subject is converted into an electrical echo signal expressed by a voltage change and output.
  • the ultrasonic endoscope 2 has an imaging optical system and an imaging element, and is inserted into the digestive tract (esophagus, stomach, duodenum, large intestine) or respiratory organs (trachea, bronchus) of the subject, and is inserted into the digestive tract or the digestive tract. , It is possible to perform either respiratory imaging.
  • the ultrasonic endoscope 2 has a light guide that guides the illumination light to irradiate the subject at the time of imaging. The tip of the light guide reaches the tip of the insertion portion of the ultrasonic endoscope 2 into the subject, while the proximal end is connected to the light source device 6 that generates illumination light.
  • the ultrasonic endoscope 2 transmits ultrasonic waves to the gastrointestinal tract and organs around the respiratory organs (pancreatic duct, gallbladder, bile duct, biliary tract, lymph node, mediastinal organ, blood vessel, etc.), and the periphery thereof. Receives ultrasonic waves reflected by the organ.
  • the curved portion 212 can bend the longitudinal axis of the tip portion 211 in two different directions from each other.
  • the curved portion 212 can be curved on the XY plane shown in FIG. 1 to change the direction of the tip portion 211, and can be curved on the XY plane orthogonal to the XY plane to change the direction of the tip portion 211. Is.
  • the ultrasonic vibrator 7 is a convex type in which a plurality of piezoelectric elements are provided in an array, the piezoelectric elements involved in transmission / reception are electronically switched, and the transmission / reception of each piezoelectric element is delayed to electronically scan. It is an ultrasonic transducer of.
  • FIG. 2 is a perspective view schematically showing the tip configuration of the insertion portion of the ultrasonic endoscope according to the first embodiment.
  • the tip portion 211 includes an ultrasonic oscillator module 214 holding an ultrasonic oscillator 7, and an endoscope module 215 having an illumination lens 218 that collects illumination light and emits it to the outside.
  • the endoscope module 215 is provided in the tip member 216, forms a part of the image pickup optical system, and collects the objective lens 217, the image pickup element, and the illumination light that captures the light from the outside and emits the illumination light to the outside. It has an illumination lens 218.
  • the tip member 216 is formed with a treatment tool protrusion 219 that communicates with the treatment tool insertion passage formed in the insertion portion 21 and projects the treatment tool from the tip of the insertion portion 21.
  • the universal cord 23 is a cable extending from the operation unit 22 and having a plurality of signal cables for transmitting various signals, an optical fiber for transmitting illumination light supplied from the light source device 6, and the like.
  • the connector 24 is provided at the tip of the universal cord 23.
  • the connector 24 includes first to third connector portions 241 to 243 to which the ultrasonic cable 31, the video cable 41, and the optical fiber cable 61 are connected, respectively.
  • the ultrasonic observation device 3 is electrically connected to the ultrasonic endoscope 2 via the ultrasonic cable 31 (FIG. 1), and sends a pulse signal to the ultrasonic endoscope 2 via the ultrasonic cable 31. At the same time as outputting, an echo signal is input from the ultrasonic endoscope 2. Then, the ultrasonic observation device 3 performs a predetermined process on the echo signal to generate ultrasonic image data.
  • the display device 5 is configured by using a liquid crystal display or an organic EL (Electro Luminescence), a projector, a CRT (Cathode Ray Tube), or the like, and an ultrasonic image generated by the ultrasonic observation device 3 or an endoscopic observation device 4 Display the endoscopic image etc. generated in.
  • a liquid crystal display or an organic EL (Electro Luminescence), a projector, a CRT (Cathode Ray Tube), or the like and an ultrasonic image generated by the ultrasonic observation device 3 or an endoscopic observation device 4 Display the endoscopic image etc. generated in.
  • the light source device 6 is connected to the ultrasonic endoscope 2 via the optical fiber cable 61 (see FIG. 1), and the illumination light that illuminates the inside of the subject via the optical fiber cable 61 is the ultrasonic endoscope. Supply to 2.
  • FIG. 3 is a cross-sectional view of the ultrasonic endoscope 2 of FIG. 2 in the longitudinal axis direction
  • FIG. 4 is an enlarged view of part A of FIG.
  • the longitudinal axis referred to here is an axis along the longitudinal direction of the insertion portion 21.
  • the insertion passage for the treatment tool is composed of a through hole 220 of the tip member 216, a through hole 153 of the base 150, a through hole 154, and a through hole 171 of the channel tube 170.
  • the vicinity of the end portion connected to the treatment tool protrusion 219 is inclined with respect to the longitudinal axis of the insertion portion 21, and the treatment tool is inclined from the treatment tool protrusion 219 with respect to the longitudinal axis. It is provided so as to protrude from the surface. Further, a treatment tool entry port 224 parallel to the longitudinal axis is provided at the end portion of the through hole 220 on the base end side.
  • the tip side referred to here is the ultrasonic module 214 side of the insertion portion 21, and the base end side is the operation portion 22 side.
  • the base 150 has a first base portion 151 and a second base portion 152.
  • the first mouthpiece portion 151 is arranged on the tip end side and is fitted to the treatment tool entrance 224.
  • the through hole 153 in the first base portion 151 is inclined with respect to the longitudinal axis.
  • the second base portion 152 is arranged on the base end side and has a smaller outer diameter than the first base portion 151.
  • the through hole 154 in the second base portion 152 and the second base portion 152 is parallel to the longitudinal axis.
  • a stepped portion 152a is provided over the entire circumference on the tip end side of the second cap portion 152, that is, on the outer periphery of the first cap portion 151 side, and the end portion on the tip side of the channel tube 170 outerly placed on the second cap portion 152. Is wound and fixed to the step portion 152a with a thread 160.
  • the base end side region 152b of the second base portion 152 has a tapered shape in which the diameter of the through hole 154 is large on the base end side.
  • the first base portion 151 is fixedly bonded to the treatment tool entrance 224 with an adhesive in a state of being fixed by the screw 225.
  • the screw 225 contact surface of the first base portion 151 is provided with a recessed portion 151x that is one step recessed from the other outer peripheral surface so that the base 150 does not come off with respect to the tip member 216 when temporarily fixed by the screw 225. May be.
  • the pressing member 100 protrudes in the longitudinal axis direction from the first main body portion 101 arranged on the outer periphery of the proximal end side region 152b of the second cap portion 152 covered by the channel tube 170 and the proximal end side of the cap 150. It has a second main body portion 102 to be arranged, and has a tubular shape. On the inner circumference of the second main body 102 of the pressing member 100, the outer diameter D 2 of the channel tube 170 near the base end side of the base 150 is smaller than the outer diameter D 7 of the channel tube 170 in contact with the first main body 101. A protrusion 103 is formed (see FIG. 5).
  • the base end side of the protrusion 103 forms a tapered surface 105 that guides the outer diameter of the channel tube 170 to gradually expand.
  • the first main body portion 101 and the second main body portion 102 may be integrally molded, but the first main body portion 101 and the second main body portion 102 manufactured as separate bodies may be joined to each other. ..
  • FIG. 6 is a cross-sectional view of, for example, a conventional ultrasonic endoscope that does not correspond to the embodiment of the present invention.
  • the pressing member 100F of FIG. 6 is different from the pressing member 100 used in the present invention in that a tapered surface is not formed on the base end side of the protrusion 103.
  • the holding member 100F is used, the swelling of the channel tube 170 by the sheath 180 near the base end side of the base 150 of the channel tube 170 can be prevented, but the swelling of the channel tube 170 extending from the base end side of the holding member 100F is caused by the sheath 180. As shown in FIG.
  • the tip of the sheath 180 may be caught by the end of the holding member 100F instead of the end of the base 150.
  • the proximal end side of the protrusion 103 is the tapered surface 105, the channel tube 170 extending from the proximal end side of the pressing member 100 is pressed by the tip of the sheath 180. Even when the sheath 180 is inflated, it is possible to effectively prevent the stack in which the tip of the sheath 180 is caught in the end of the pressing member 100.
  • the inner diameter D 3 of the protrusion 103 portion of the pressing member 100 is about the same as the outer diameter D 0 of the channel tube 170.
  • the channel tube 170 is expanded even at the portion in contact with the protrusion 103 by inserting the sheath 180, and the end portion of the base 150 is expanded. Is exposed, and there is a high possibility that the tip of the sheath 170 will get stuck.
  • the inner diameter D 3 at the protrusion 103 portion is smaller than the outer diameter D 0 of the channel tube 170, the inner diameter D 4 at the portion of the channel tube 170 in contact with the protrusion 103 becomes smaller, and the insertion of the sheath 180 deteriorates.
  • the assembleability for inserting the pressing member 100 is also reduced.
  • the inner diameter D 5 of the end portion of the base end side region 152b of the base 150 is the inner diameter D 4 at the portion in contact with the protrusion 103 of the channel tube 170.
  • the inner diameter D 4 at the portion of the channel tube 170 in contact with the protrusion 103 is the original diameter of the channel tube 170 due to the relationship between the inner diameter D 3 of the protrusion 103 of the pressing member 100 and the outer diameter D 0 of the channel tube 170. Since it may be different from the inner diameter D 1 , it is preferable to set the inner diameter D 5 and the inner diameter D 4 in consideration of the relevant values.
  • an adhesive is used when fixing the channel tube 170 to the base 150, it is preferable to consider the thickness of the adhesive.
  • the inner diameter D 6 of the first main body portion 101 of the pressing member 100 is about the same as the outer diameter D 7 of the channel tube 170 covering the base end side region 152b of the base 150. If the inner diameter D 6 of the first main body 101 is larger than the outer diameter D 7 of the channel tube 170, a gap is generated between the channel tube 170 and the holding member 100, so that the holding member 100 is eccentric from the base 150. There is a risk of tilting and assembling. In such a case, the holding of the channel tube 170 by the pressing member 100 may not be successful, resulting in poor insertion of the sheath 180. Further, if the inner diameter D 6 of the first main body portion 101 is smaller than the outer diameter D 7 of the channel tube 170, it is necessary to compress the channel tube 170 when assembling the holding member 100 to the base 150, which makes assembly difficult. Become.
  • the difference between the inner diameter D 6 of the first main body portion 101 of the pressing member 100 and the outer diameter D 8 of the base end side region 152b of the base 150 is not more than twice the wall thickness t of the channel tube 170 in the natural state. Is preferable.
  • FIG. 7 is a diagram illustrating the curvature of the curved portion 212 of the ultrasonic endoscope 2 of FIG.
  • the curved portion 212 is configured by connecting a plurality of curved pieces (not shown), and is curved in the vertical and horizontal directions by operating the curved knob 221 (see FIG. 1).
  • the curved portion is configured by connecting a plurality of curved pieces having the same shape, but in the curved portion 212 of the ultrasonic endoscope 2 of the present invention, the distance between the curved pieces arranged on the tip side is the base end. Use one that is smaller than the distance between the curved pieces placed on the side. As shown in FIG.
  • the diameter of the curved portion 212 is about 15 mm, which is 13 mm.
  • the length of the curved portion 212 is about 40 mm in the conventional one, which was about 50 mm, and the maximum bending angle is 130 ° or more, and further 150 ° from the one in which the conventional one was about 90 °.
  • the ultrasonic endoscope 2 modified to the above degree has come to be used.
  • the angle formed between the adjacent curved pieces in the curved state is also significantly increased.
  • the diameter of the curved portion 212 has been reduced, and even when the bending angle is small, the tip portion of the sheath 180 is likely to be caught on the end portion of the pressing member 100.
  • the angle formed between the adjacent curved pieces in the curved state becomes smaller. It is possible to prevent the tip portion of the sheath 180 from being caught on the end portion of the pressing member 100.
  • the diameter of the curved portion 212 is reduced, the diameter of a plurality of signal cables for supplying power to the ultrasonic module 214 and the image pickup module 215 and transmitting various signals is also reduced, but the cable is less elastic due to the reduction in diameter. It may be a structure. Such a signal cable is more likely to buckle and break due to the bending operation of the bending portion 212 which is shortened and the bending angle is increased. From the viewpoint of preventing disconnection of the signal cable, it is preferable to cover the periphery of the signal cable arranged in the curved portion 212 with a heat-shrinkable tube that can be curved but is hard.
  • FIG. 8 is a top view illustrating a modification 1 of the endoscope according to the embodiment of the present invention
  • FIG. 9 is a cross-sectional view of FIG.
  • the holding member 100A according to the first modification has an index indicating the mounting position on the outer surface.
  • the pressing member 100A has a first main body portion 101A and a second main body portion 102, and the second main body portion 102A is configured to have a larger outer diameter than the first main body portion.
  • the boundary line between the first main body portion 101A and the second main body portion 102A serves as an index indicating the mounting position of the pressing member 100A.
  • the pressing member 100A has an index, that is, a notch 106 that crosses the first main body portion 101A and the second main body portion 102A. As shown in FIG. 8, the notch 106 is a notch that penetrates from the outer surface to the inner surface of the pressing member 106A.
  • the pressing member 100A is assembled to the proximal end side region 152b of the base 150 covered with the channel tube 170, the proximal end side region 152b visible through the transparent channel tube 170 from the notch 106 is confirmed, and the proximal end and the index are confirmed. Assemble the pressing member 100A so that the index is located on the tip side from the base end. This makes it possible to easily attach the holding member 100A to the base 150 at an accurate position.
  • the first main body portion 101A and the second main body portion 102A are used as indexes as different outer diameters, but the index is not limited to this.
  • a groove formed by a laser or the like or an index may be formed by printing or the like at the boundary between the first main body portion and the second main body portion formed to have the same diameter.
  • the notch 106 is preferably arranged on the UP side having the largest bending angle in order to prevent the tip portion of the sheath 180 from being caught in the notch 106.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Biomedical Technology (AREA)
  • Medical Informatics (AREA)
  • Optics & Photonics (AREA)
  • Pathology (AREA)
  • Radiology & Medical Imaging (AREA)
  • Biophysics (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Molecular Biology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Ultra Sonic Daignosis Equipment (AREA)
  • Endoscopes (AREA)

Abstract

Provided is an endoscope in which snagging of a sheath on a cap can be prevented by a simple configuration. An endoscope according to the present invention is provided with: a channel tube which is inserted through a treatment tool; a cap that has the leading end side thereof fitted to the base end side of an opening in a leading end member of an insertion part, that has the base end side covered by the channel tube, and that has a through-hole that, along with the opening and the channel tube, constitutes an insertion channel for the treatment tool; and a cylindrical pressing member which comprises a first body part that is disposed around the outer circumference of the cap being covered by the channel tube and a second body part that is disposed so as to protrude beyond the base end side of the cap in a longitudinal direction. The pressing member has formed on an inner circumference of the second body part a protrusion that performs pressing so as to cause the outer diameter of the channel tube extending toward the base end side to become smaller than the outer diameter of the channel tube that is in contact with the first body part. The base end side of the protrusion is configured to have a tapered surface that works to guide the channel tube in such a manner as to gradually increase the outer diameter thereof.

Description

内視鏡Endoscope
 本発明は、内視鏡に関する。 The present invention relates to an endoscope.
 従来、内視鏡は、挿入部を患者等の被検体内に挿入することによって、撮像装置による被検体内の画像データの取得や、処置具等による治療を行っている。処置具を挿通する処置具用挿通路は、内視鏡挿入部の先端部材の開口に口金を介して、樹脂製のチャンネルチューブが組み付けられるものであるが、口金の基端側にチャンネルチューブを被せて、樹脂による接着や糸で縛ることでチャンネルチューブの脱落を防止している。 Conventionally, an endoscope has an insertion part inserted into a subject such as a patient to acquire image data in the subject by an imaging device and to perform treatment with a treatment tool or the like. The insertion passage for the treatment tool through which the treatment tool is inserted is such that a resin channel tube is attached to the opening of the tip member of the endoscope insertion portion via a mouthpiece, and the channel tube is attached to the base end side of the mouthpiece. The channel tube is prevented from falling off by covering it with resin or tying it with a thread.
 近年、被検体への影響をより小さくし、かつ撮像装置や処置具の患部へのコンタクトの容易さの観点から、湾曲部の短小化、細径化、および湾曲角度の増大が求められている。湾曲部の短小化、細径化、および湾曲角度が増大した結果、湾曲部を湾曲させた状態で処置具を処置具用挿通路に挿通すると、図13に示すように、処置具を内蔵したシース180の先端により、チャンネルチューブ170が押し広げられて湾曲方向と反対側に膨らみ、さらにシース180を先端側に挿通すると、図14に示すように、口金150の基端側にシース180の先端部が引っかかるスタックが発生するおそれがあり、その場合シース180の挿脱がし難いという問題を有していた。 In recent years, from the viewpoint of reducing the influence on the subject and facilitating contact of the imaging device or treatment tool with the affected area, it has been required to shorten the curved portion, reduce the diameter, and increase the bending angle. .. As a result of shortening the bending portion, reducing the diameter, and increasing the bending angle, when the treatment tool is inserted into the insertion passage for the treatment tool with the curved portion curved, the treatment tool is built in as shown in FIG. When the channel tube 170 is expanded and swells in the direction opposite to the bending direction by the tip of the sheath 180 and the sheath 180 is further inserted toward the tip side, the tip of the sheath 180 is on the base end side of the base 150 as shown in FIG. There is a possibility that a stack in which the portion is caught may occur, and in that case, there is a problem that it is difficult to insert or remove the sheath 180.
 これに対し、先端部本体に設けられた処置具導出口に連通されるパイプ部材と、前記パイプ部材に接続される処置具挿通用チューブと、を備え、前記パイプ部材の先端側に形成される第1領域を、基端側に形成される第2領域よりも耐圧潰性が高い領域とした内視鏡が提案されている(例えば、特許文献1参照)。特許文献1では、処置具を内蔵するシースを処置具挿通用チューブに挿通した際の第1領域の変形を抑制することができるため、シースのパイプ部材への引っかかりを防止することができる。 On the other hand, a pipe member communicating with the treatment tool outlet provided in the tip body and a treatment tool insertion tube connected to the pipe member are provided and formed on the tip side of the pipe member. An endoscope has been proposed in which the first region is a region having a higher pressure resistance than the second region formed on the proximal end side (see, for example, Patent Document 1). In Patent Document 1, since deformation of the first region when the sheath containing the treatment tool is inserted into the treatment tool insertion tube can be suppressed, it is possible to prevent the sheath from being caught in the pipe member.
特開2018-134276号公報Japanese Unexamined Patent Publication No. 2018-134276
 しかしながら、特許文献1では、第1領域を、基端側に形成される第2領域よりも耐圧潰性が高い領域とする工程が必要となり、また、第1領域は耐圧潰性が高いため、パイプ部材への接続が困難になるという問題を有している。 However, in Patent Document 1, a step is required in which the first region has a higher pressure-resistant crushing property than the second region formed on the proximal end side, and the first region has a higher pressure-resistant crushing property. It has a problem that it becomes difficult to connect to a pipe member.
 本発明は、上記に鑑みてなされたものであって、簡易な構成で、口金へのシースの引っかかりを防止しうる内視鏡を提供することを目的とする。 The present invention has been made in view of the above, and an object of the present invention is to provide an endoscope having a simple structure and capable of preventing the sheath from being caught in the mouthpiece.
 上述した課題を解決し、目的を達成するために、本発明に係る内視鏡は、被検体内に挿入され先端側に先端部材を有する挿入部の長手方向の先端側と基端側とを連通し、処置具を挿通するチャンネルチューブと、先端側が前記先端部材の開口の基端側に篏合され、基端側が前記チャンネルチューブに被覆され、前記開口および前記チャンネルチューブとともに前記処置具の挿通路を構成する貫通孔を有する口金と、前記チャンネルチューブにより被覆された前記口金の外周の周囲に配置される第1本体部と、前記口金の基端側よりも前記長手方向に突出して配置される第2本体部とを有する、筒状の押さえ部材と、を備え、前記押さえ部材の第2本体部の内周には、基端側に延出する前記チャンネルチューブの外径を、前記第1本体部と接する前記チャンネルチューブの外径より小さくするように押圧する突起が形成され、前記突起の基端側は、前記チャンネルチューブの外径が徐々に広がるように案内するテーパ面をなす。 In order to solve the above-mentioned problems and achieve the object, the endoscope according to the present invention has a distal end side and a proximal end side in the longitudinal direction of an insertion portion inserted into a subject and having a distal end member on the distal end side. The channel tube through which the treatment tool is inserted and the channel tube are aligned with the proximal end side of the opening of the distal end member, the proximal end side is covered with the channel tube, and the treatment instrument is inserted together with the opening and the channel tube. A mouthpiece having a through hole constituting a passage, a first main body portion arranged around the outer periphery of the mouthpiece covered with the channel tube, and a base portion protruding from the base end side of the mouthpiece in the longitudinal direction are arranged. A tubular holding member having a second main body portion is provided, and the outer diameter of the channel tube extending toward the proximal end side is set on the inner circumference of the second main body portion of the holding member. 1 A protrusion is formed to press the channel tube so as to be smaller than the outer diameter of the channel tube in contact with the main body, and the base end side of the protrusion forms a tapered surface that guides the outer diameter of the channel tube to gradually expand.
 また、本発明に係る内視鏡は、上記発明において、前記押さえ部材は、前記第1本体部と前記第2本体部とを接合してなる。 Further, in the endoscope according to the present invention, in the above invention, the holding member is formed by joining the first main body portion and the second main body portion.
 また、本発明に係る内視鏡は、上記発明において、前記押さえ部材の外表面に、前記口金との取付位置を示す指標が配設されている。 Further, in the endoscope according to the present invention, in the above invention, an index indicating the mounting position with the mouthpiece is arranged on the outer surface of the holding member.
 また、本発明に係る内視鏡は、上記発明において、前記押さえ部材は、前記指標を横断した切り欠きを有する。 Further, in the endoscope according to the present invention, in the above invention, the holding member has a notch across the index.
 また、本発明に係る内視鏡は、上記発明において、前記第1本体部の内径と前記口金の基端側の外径との差は、自然状態での前記チャンネルチューブの肉厚の2倍以下である。 Further, in the endoscope according to the present invention, in the above invention, the difference between the inner diameter of the first main body and the outer diameter of the base end side of the mouthpiece is twice the wall thickness of the channel tube in the natural state. It is as follows.
 また、本発明に係る内視鏡は、上記発明において、前記口金は、前記チャンネルチューブと接触するための突き当て面を有する。 Further, in the endoscope according to the present invention, in the above invention, the mouthpiece has an abutting surface for contacting with the channel tube.
 また、本発明に係る内視鏡は、上記発明において、湾曲部の最大湾曲角度が130°以上である。 Further, in the endoscope according to the present invention, the maximum bending angle of the curved portion is 130 ° or more in the above invention.
 また、本発明に係る内視鏡は、上記発明において、前記湾曲部は複数の湾曲駒を連結して構成され、先端側に配置される湾曲駒の間隔は、基端側に配置される湾曲駒の間隔より小さい。 Further, in the endoscope according to the present invention, in the above invention, the curved portion is configured by connecting a plurality of curved pieces, and the distance between the curved pieces arranged on the tip end side is that of the curved piece arranged on the proximal end side. Less than the interval.
 本発明によれば、簡易な構成で、処置具を内蔵したシースの口金への引っかかりを防止しうる内視鏡を実現することができる。 According to the present invention, it is possible to realize an endoscope having a simple configuration and capable of preventing the sheath having a built-in treatment tool from being caught in the mouthpiece.
図1は、本発明の実施の形態に係る内視鏡システムを模式的に示す図である。FIG. 1 is a diagram schematically showing an endoscope system according to an embodiment of the present invention. 図2は、本発明の実施の形態に係る超音波内視鏡の挿入部の先端構成を模式的に示す斜視図である。FIG. 2 is a perspective view schematically showing the tip configuration of the insertion portion of the ultrasonic endoscope according to the embodiment of the present invention. 図3は、図2の超音波内視鏡の断面図である。FIG. 3 is a cross-sectional view of the ultrasonic endoscope of FIG. 図4は、図3のAの拡大図である。FIG. 4 is an enlarged view of A in FIG. 図5は、図4において押さえ部材を取り外した状態の断面図である。FIG. 5 is a cross-sectional view of FIG. 4 in a state where the holding member is removed. 図6は、本発明の実施の形態に該当しない超音波内視鏡の断面図である。FIG. 6 is a cross-sectional view of an ultrasonic endoscope that does not correspond to the embodiment of the present invention. 図7は、図2の内視鏡の湾曲部の湾曲を説明する図である。FIG. 7 is a diagram illustrating the curvature of the curved portion of the endoscope of FIG. 図8は、本発明の実施の形態に係る内視鏡の変形例1を説明する上面図である。FIG. 8 is a top view illustrating a modification 1 of the endoscope according to the embodiment of the present invention. 図9は、図8の断面図である。FIG. 9 is a cross-sectional view of FIG. 図10は、本実施の形態の変形例2に係る内視鏡の上面図である。FIG. 10 is a top view of the endoscope according to the second modification of the present embodiment. 図11は、本実施の形態の変形例3に係る内視鏡の上面図である。FIG. 11 is a top view of the endoscope according to the third modification of the present embodiment. 図12は、本実施の形態の変形例4に係る内視鏡の上面図である。FIG. 12 is a top view of the endoscope according to the modified example 4 of the present embodiment. 図13は、従来技術に係る内視鏡の湾曲を説明する断面図である。FIG. 13 is a cross-sectional view illustrating the curvature of the endoscope according to the prior art. 図14は、従来技術に係る内視鏡の湾曲を説明する断面図である。FIG. 14 is a cross-sectional view illustrating the curvature of the endoscope according to the prior art.
 以下に、図面を参照して本発明に係る内視鏡の実施の形態を説明する。なお、これらの実施の形態により本発明が限定されるものではない。また、図面の記載において、同一又は対応する要素には適宜同一の符号を付している。また、図面は模式的なものであり、各要素の寸法の関係、各要素の比率等は、現実と異なる場合があることに留意する必要がある。図面の相互間においても、互いの寸法の関係や比率が異なる部分が含まれている場合がある。 Hereinafter, embodiments of the endoscope according to the present invention will be described with reference to the drawings. The present invention is not limited to these embodiments. Further, in the description of the drawings, the same or corresponding elements are appropriately designated by the same reference numerals. In addition, it should be noted that the drawings are schematic, and the relationship between the dimensions of each element, the ratio of each element, etc. may differ from the reality. Even between the drawings, there may be parts where the relationship and ratio of the dimensions are different from each other.
(実施の形態)
 図1は、本発明の実施の形態に係る内視鏡システム1を模式的に示す図である。内視鏡システム1は、超音波内視鏡を用いて生体の管腔等の被検体内の超音波診断を行うシステムである。この内視鏡システム1は、図1に示すように、超音波内視鏡2と、超音波観測装置3と、内視鏡観察装置4と、表示装置5と、光源装置6とを備える。
(Embodiment)
FIG. 1 is a diagram schematically showing an endoscope system 1 according to an embodiment of the present invention. The endoscope system 1 is a system for performing ultrasonic diagnosis in a subject such as a cavity of a living body using an ultrasonic endoscope. As shown in FIG. 1, the endoscope system 1 includes an ultrasonic endoscope 2, an ultrasonic observation device 3, an endoscope observation device 4, a display device 5, and a light source device 6.
 超音波内視鏡2は、その先端部に設けられた超音波振動子によって、超音波観測装置3から受信した電気的なパルス信号を超音波パルス(音響パルス)に変換して被検体へ照射するとともに、被検体で反射された超音波エコーを電圧変化で表現する電気的なエコー信号に変換して出力する。 The ultrasonic endoscope 2 converts an electrical pulse signal received from the ultrasonic observation device 3 into an ultrasonic pulse (acoustic pulse) by an ultrasonic vibrator provided at the tip thereof and irradiates the subject. At the same time, the ultrasonic echo reflected by the subject is converted into an electrical echo signal expressed by a voltage change and output.
 超音波内視鏡2は、撮像光学系および撮像素子を有しており、被検体の消化管(食道、胃、十二指腸、大腸)、または呼吸器(気管、気管支)へ挿入され、消化管や、呼吸器のいずれかの撮像を行うことが可能である。超音波内視鏡2は、撮像時に被検体へ照射する照明光を導くライトガイドを有する。このライトガイドは、先端部が超音波内視鏡2の被検体への挿入部の先端まで達している一方、基端部が照明光を発生する光源装置6に接続されている。また、超音波内視鏡2は、消化管や、呼吸器の周囲臓器(膵臓、胆嚢、胆管、胆道、リンパ節、縦隔臓器、血管等)に対して、超音波を送信し、該周辺臓器で反射した超音波を受信する。 The ultrasonic endoscope 2 has an imaging optical system and an imaging element, and is inserted into the digestive tract (esophagus, stomach, duodenum, large intestine) or respiratory organs (trachea, bronchus) of the subject, and is inserted into the digestive tract or the digestive tract. , It is possible to perform either respiratory imaging. The ultrasonic endoscope 2 has a light guide that guides the illumination light to irradiate the subject at the time of imaging. The tip of the light guide reaches the tip of the insertion portion of the ultrasonic endoscope 2 into the subject, while the proximal end is connected to the light source device 6 that generates illumination light. Further, the ultrasonic endoscope 2 transmits ultrasonic waves to the gastrointestinal tract and organs around the respiratory organs (pancreatic duct, gallbladder, bile duct, biliary tract, lymph node, mediastinal organ, blood vessel, etc.), and the periphery thereof. Receives ultrasonic waves reflected by the organ.
 超音波内視鏡2は、図1に示すように、挿入部21と、操作部22と、ユニバーサルコード23と、コネクタ24とを備える。挿入部21は、被検体内に挿入される部分である。この挿入部21は、図1に示すように、先端側に設けられ、超音波振動子7を含む硬性の先端部211と、先端部211の基端側に連結され湾曲可能とする湾曲部212と、湾曲部212の基端側に連結され可撓性を有する可撓管部213とを備える。ここで、挿入部21の内部には、光源装置6から供給された照明光を伝送するライトガイド、各種信号を伝送する複数の信号線が引き回されているとともに、処置具を挿通するための処置具用チャンネルなどが形成されている。湾曲部212は、先端部211の長手軸を互いに異なる二方向に湾曲可能である。湾曲部212は、例えば図1に示すXY平面上で湾曲して先端部211の向きを変更可能であるとともに、このXY平面と直交するXZ平面上で湾曲して先端部211の向きを変更可能である。 As shown in FIG. 1, the ultrasonic endoscope 2 includes an insertion unit 21, an operation unit 22, a universal cord 23, and a connector 24. The insertion portion 21 is a portion to be inserted into the subject. As shown in FIG. 1, the insertion portion 21 is provided on the tip end side, and is connected to the rigid tip portion 211 including the ultrasonic vibrator 7 and the base end side of the tip portion 211 so as to be bendable. And a flexible tube portion 213 connected to the base end side of the curved portion 212 and having flexibility. Here, inside the insertion portion 21, a light guide for transmitting the illumination light supplied from the light source device 6 and a plurality of signal lines for transmitting various signals are routed, and for inserting a treatment tool. Channels for treatment tools and the like are formed. The curved portion 212 can bend the longitudinal axis of the tip portion 211 in two different directions from each other. For example, the curved portion 212 can be curved on the XY plane shown in FIG. 1 to change the direction of the tip portion 211, and can be curved on the XY plane orthogonal to the XY plane to change the direction of the tip portion 211. Is.
 超音波振動子7は、複数の圧電素子をアレイ状に設け、送受信にかかわる圧電素子を電子的に切り替えたり、各圧電素子の送受信に遅延をかけたりすることで、電子的に走査させるコンベックス型の超音波振動子である。 The ultrasonic vibrator 7 is a convex type in which a plurality of piezoelectric elements are provided in an array, the piezoelectric elements involved in transmission / reception are electronically switched, and the transmission / reception of each piezoelectric element is delayed to electronically scan. It is an ultrasonic transducer of.
 図2は、本実施の形態1に係る超音波内視鏡の挿入部の先端構成を模式的に示す斜視図である。図2に示すように、先端部211は、超音波振動子7を保持する超音波振動子モジュール214と、照明光を集光して外部に出射する照明レンズ218を有する内視鏡モジュール215と、を備える。内視鏡モジュール215は、先端部材216内に設けられ、撮像光学系の一部をなし、外部からの光を取り込む対物レンズ217、撮像素子、および、照明光を集光して外部に出射する照明レンズ218を有する。また、先端部材216には、挿入部21内に形成された処置具用挿通路に連通し、挿入部21の先端から処置具を突出させる処置具突出口219が形成されている。 FIG. 2 is a perspective view schematically showing the tip configuration of the insertion portion of the ultrasonic endoscope according to the first embodiment. As shown in FIG. 2, the tip portion 211 includes an ultrasonic oscillator module 214 holding an ultrasonic oscillator 7, and an endoscope module 215 having an illumination lens 218 that collects illumination light and emits it to the outside. , Equipped with. The endoscope module 215 is provided in the tip member 216, forms a part of the image pickup optical system, and collects the objective lens 217, the image pickup element, and the illumination light that captures the light from the outside and emits the illumination light to the outside. It has an illumination lens 218. Further, the tip member 216 is formed with a treatment tool protrusion 219 that communicates with the treatment tool insertion passage formed in the insertion portion 21 and projects the treatment tool from the tip of the insertion portion 21.
 図1に戻り、操作部22は、挿入部21の基端側に連結され、医師等のユーザからの各種操作を受け付ける部分である。この操作部22は、図1に示すように、湾曲部212を湾曲操作するための湾曲ノブ221と、各種操作を行うための複数の操作部材222とを備える。また、操作部22には、処置具用挿通路に連通し、当該処置具用挿通路に処置具を挿通するための処置具挿入口223が形成されている。 Returning to FIG. 1, the operation unit 22 is connected to the base end side of the insertion unit 21 and is a part that receives various operations from users such as doctors. As shown in FIG. 1, the operation unit 22 includes a bending knob 221 for performing a bending operation on the bending portion 212, and a plurality of operating members 222 for performing various operations. Further, the operation unit 22 is formed with a treatment tool insertion port 223 that communicates with the treatment tool insertion passage and inserts the treatment tool into the treatment tool insertion passage.
 ユニバーサルコード23は、操作部22から延在し、各種信号を伝送する複数の信号ケーブル、および光源装置6から供給された照明光を伝送する光ファイバ等が配設されたケーブルである。 The universal cord 23 is a cable extending from the operation unit 22 and having a plurality of signal cables for transmitting various signals, an optical fiber for transmitting illumination light supplied from the light source device 6, and the like.
 コネクタ24は、ユニバーサルコード23の先端に設けられている。そして、コネクタ24は、超音波ケーブル31、ビデオケーブル41、および光ファイバケーブル61がそれぞれ接続される第1~第3コネクタ部241~243を備える。 The connector 24 is provided at the tip of the universal cord 23. The connector 24 includes first to third connector portions 241 to 243 to which the ultrasonic cable 31, the video cable 41, and the optical fiber cable 61 are connected, respectively.
 超音波観測装置3は、超音波ケーブル31(図1)を経由して超音波内視鏡2に電気的に接続し、超音波ケーブル31を経由して超音波内視鏡2にパルス信号を出力するとともに超音波内視鏡2からエコー信号を入力する。そして、超音波観測装置3は、当該エコー信号に所定の処理を施して超音波画像データを生成する。 The ultrasonic observation device 3 is electrically connected to the ultrasonic endoscope 2 via the ultrasonic cable 31 (FIG. 1), and sends a pulse signal to the ultrasonic endoscope 2 via the ultrasonic cable 31. At the same time as outputting, an echo signal is input from the ultrasonic endoscope 2. Then, the ultrasonic observation device 3 performs a predetermined process on the echo signal to generate ultrasonic image data.
 内視鏡観察装置4は、ビデオケーブル41(図1参照)を経由して超音波内視鏡2に電気的に接続し、ビデオケーブル41を経由して超音波内視鏡2からの画像信号を入力する。そして、内視鏡観察装置4は、当該画像信号に所定の処理を施して内視鏡画像データを生成する。 The endoscope observation device 4 is electrically connected to the ultrasonic endoscope 2 via a video cable 41 (see FIG. 1), and an image signal from the ultrasonic endoscope 2 via the video cable 41. Enter. Then, the endoscope observation device 4 performs a predetermined process on the image signal to generate endoscopic image data.
 表示装置5は、液晶または有機EL(Electro Luminescence)、プロジェクタ、CRT(Cathode Ray Tube)などを用いて構成され、超音波観測装置3にて生成された超音波画像や、内視鏡観察装置4にて生成された内視鏡画像等を表示する。 The display device 5 is configured by using a liquid crystal display or an organic EL (Electro Luminescence), a projector, a CRT (Cathode Ray Tube), or the like, and an ultrasonic image generated by the ultrasonic observation device 3 or an endoscopic observation device 4 Display the endoscopic image etc. generated in.
 光源装置6は、光ファイバケーブル61(図1参照)を経由して超音波内視鏡2に接続し、光ファイバケーブル61を経由して被検体内を照明する照明光を超音波内視鏡2に供給する。 The light source device 6 is connected to the ultrasonic endoscope 2 via the optical fiber cable 61 (see FIG. 1), and the illumination light that illuminates the inside of the subject via the optical fiber cable 61 is the ultrasonic endoscope. Supply to 2.
 図3は、図2の超音波内視鏡2の長手軸方向の断面図であり、図4は、図3のA部の拡大図である。なお、ここでいう長手軸とは、挿入部21の長手方向に沿った軸である。処置具用挿通路は、先端部材216の貫通孔220と、口金150の貫通孔153、貫通孔154と、チャンネルチューブ170の貫通孔171によって構成されている。 FIG. 3 is a cross-sectional view of the ultrasonic endoscope 2 of FIG. 2 in the longitudinal axis direction, and FIG. 4 is an enlarged view of part A of FIG. The longitudinal axis referred to here is an axis along the longitudinal direction of the insertion portion 21. The insertion passage for the treatment tool is composed of a through hole 220 of the tip member 216, a through hole 153 of the base 150, a through hole 154, and a through hole 171 of the channel tube 170.
 先端部材216の貫通孔220は、処置具突出口219に連なる端部近傍が、挿入部21の長手軸に対して傾斜し、処置具が処置具突出口219から長手軸に対して傾斜した方向に突出するように設けられている。また、貫通孔220の基端側の端部には、長手軸に対して平行な処置具突入口224が設けられている。なお、ここでいう先端側とは、挿入部21の超音波モジュール214側であり、基端側は操作部22側である。 In the through hole 220 of the tip member 216, the vicinity of the end portion connected to the treatment tool protrusion 219 is inclined with respect to the longitudinal axis of the insertion portion 21, and the treatment tool is inclined from the treatment tool protrusion 219 with respect to the longitudinal axis. It is provided so as to protrude from the surface. Further, a treatment tool entry port 224 parallel to the longitudinal axis is provided at the end portion of the through hole 220 on the base end side. The tip side referred to here is the ultrasonic module 214 side of the insertion portion 21, and the base end side is the operation portion 22 side.
 口金150は、第1口金部151と、第2口金部152とを有する。第1口金部151は、先端側に配置されて処置具突入口224に篏合される。第1口金部151内の貫通孔153は、長手軸に対して傾斜している。第2口金部152は、基端側に配置され、第1口金部151より外径が細径である。第2口金部152および第2口金部152内の貫通孔154は、長手軸に対して平行である。 The base 150 has a first base portion 151 and a second base portion 152. The first mouthpiece portion 151 is arranged on the tip end side and is fitted to the treatment tool entrance 224. The through hole 153 in the first base portion 151 is inclined with respect to the longitudinal axis. The second base portion 152 is arranged on the base end side and has a smaller outer diameter than the first base portion 151. The through hole 154 in the second base portion 152 and the second base portion 152 is parallel to the longitudinal axis.
 第2口金部152の先端側、すなわち第1口金部151側の外周には、全周にわたって段部152aが設けられ、第2口金部152に外篏されたチャンネルチューブ170の先端側の端部が糸160で段部152aに糸巻き固定されている。第2口金部152の基端側領域152bは、貫通孔154の径が基端側が大きいテーパ状をなしている。第1口金部151は、ビス225により固定された状態で、接着剤により処置具突入口224に篏合接着される。第1口金部151をビス225により仮固定した状態で、接着剤により篏合接着するため、位置ずれを防止するとともに、組み立て性を向上することができる。なお、第1口金部151のビス225当接面は他の外周面より一段凹んだ窪み部151xを設けて、ビス225による仮固定時に口金150が先端部材216に対して確実に抜けないようにしてもよい。 A stepped portion 152a is provided over the entire circumference on the tip end side of the second cap portion 152, that is, on the outer periphery of the first cap portion 151 side, and the end portion on the tip side of the channel tube 170 outerly placed on the second cap portion 152. Is wound and fixed to the step portion 152a with a thread 160. The base end side region 152b of the second base portion 152 has a tapered shape in which the diameter of the through hole 154 is large on the base end side. The first base portion 151 is fixedly bonded to the treatment tool entrance 224 with an adhesive in a state of being fixed by the screw 225. Since the first base portion 151 is temporarily fixed by the screw 225 and then bonded together with an adhesive, it is possible to prevent misalignment and improve assembleability. The screw 225 contact surface of the first base portion 151 is provided with a recessed portion 151x that is one step recessed from the other outer peripheral surface so that the base 150 does not come off with respect to the tip member 216 when temporarily fixed by the screw 225. May be.
 押さえ部材100は、チャンネルチューブ170により被覆された第2口金部152の基端側領域152bの外周に配置される第1本体部101と、口金150の基端側よりも長手軸方向に突出して配置される第2本体部102と、を有し、筒状をなしている。押さえ部材100の第2本体部102の内周には、口金150の基端側近傍のチャンネルチューブ170の外径Dを、第1本体部101と接するチャンネルチューブ170の外径Dより小さくするように押圧する突起103が形成される(図5参照)。口金150を被覆するために膨らんだチャンネルチューブ170を突起103により押圧することにより、シース180の挿入の際に、チャンネルチューブ170で口金150の端部をブロックでき、スタック抑制効果を向上することができる。突起103の基端側は、チャンネルチューブ170の外径が徐々に広がるように案内するテーパ面105をなす。第1本体部101と第2本体部102とは、一体成形されたものでもよいが、別体として製造した第1本体部101と第2本体部102とを、接合したものであってもよい。  The pressing member 100 protrudes in the longitudinal axis direction from the first main body portion 101 arranged on the outer periphery of the proximal end side region 152b of the second cap portion 152 covered by the channel tube 170 and the proximal end side of the cap 150. It has a second main body portion 102 to be arranged, and has a tubular shape. On the inner circumference of the second main body 102 of the pressing member 100, the outer diameter D 2 of the channel tube 170 near the base end side of the base 150 is smaller than the outer diameter D 7 of the channel tube 170 in contact with the first main body 101. A protrusion 103 is formed (see FIG. 5). By pressing the channel tube 170 inflated to cover the base 150 with the protrusion 103, the end of the base 150 can be blocked by the channel tube 170 when the sheath 180 is inserted, and the stack suppressing effect can be improved. can. The base end side of the protrusion 103 forms a tapered surface 105 that guides the outer diameter of the channel tube 170 to gradually expand. The first main body portion 101 and the second main body portion 102 may be integrally molded, but the first main body portion 101 and the second main body portion 102 manufactured as separate bodies may be joined to each other. ..
 図6は、本発明の実施の形態に該当しない例えば従来の超音波内視鏡の断面図である。図6の押さえ部材100Fは、突起103の基端側にテーパ面が形成されていない点で本発明で使用する押さえ部材100と異なる。押さえ部材100Fを使用した場合、チャンネルチューブ170の口金150の基端側近傍のシース180による膨らみは防止できるものの、押さえ部材100Fの基端側から延出するチャンネルチューブ170のシース180による膨らみは、図6に示すように抑制することができず、口金150の端部ではなく、押さえ部材100Fの端部にシース180の先端部が引っかかってしまうおそれがある。本発明の実施の形態で使用する押さえ部材100では、突起103の基端側はテーパ面105であるため、押さえ部材100の基端側から延出するチャンネルチューブ170が、シース180の先端により押圧されて膨らんだ場合でも、押さえ部材100の端部にシース180の先端部が引っかかるスタックを効果的に防止することができる。 FIG. 6 is a cross-sectional view of, for example, a conventional ultrasonic endoscope that does not correspond to the embodiment of the present invention. The pressing member 100F of FIG. 6 is different from the pressing member 100 used in the present invention in that a tapered surface is not formed on the base end side of the protrusion 103. When the holding member 100F is used, the swelling of the channel tube 170 by the sheath 180 near the base end side of the base 150 of the channel tube 170 can be prevented, but the swelling of the channel tube 170 extending from the base end side of the holding member 100F is caused by the sheath 180. As shown in FIG. 6, it cannot be suppressed, and the tip of the sheath 180 may be caught by the end of the holding member 100F instead of the end of the base 150. In the pressing member 100 used in the embodiment of the present invention, since the proximal end side of the protrusion 103 is the tapered surface 105, the channel tube 170 extending from the proximal end side of the pressing member 100 is pressed by the tip of the sheath 180. Even when the sheath 180 is inflated, it is possible to effectively prevent the stack in which the tip of the sheath 180 is caught in the end of the pressing member 100.
 本実施の形態において、押さえ部材100の突起103部分での内径Dは、チャンネルチューブ170の外径Dと同程度であることが好ましい。突起103部分での内径Dが、チャンネルチューブ170の外径Dより大きいと、チャンネルチューブ170は、突起103と接している部分においてもシース180の挿通により押し広げられ、口金150の端部が露出し、シース170の先端部がスタックするおそれが高くなる。また、突起103部分での内径Dが、チャンネルチューブ170の外径Dより小さいと、チャンネルチューブ170の突起103と接する部分での内径Dが小さくなり、シース180の挿通が悪化するとともに、押さえ部材100を挿入する組み立て性も低下する。 In the present embodiment, it is preferable that the inner diameter D 3 of the protrusion 103 portion of the pressing member 100 is about the same as the outer diameter D 0 of the channel tube 170. When the inner diameter D 3 at the protrusion 103 portion is larger than the outer diameter D 0 of the channel tube 170, the channel tube 170 is expanded even at the portion in contact with the protrusion 103 by inserting the sheath 180, and the end portion of the base 150 is expanded. Is exposed, and there is a high possibility that the tip of the sheath 170 will get stuck. Further, when the inner diameter D 3 at the protrusion 103 portion is smaller than the outer diameter D 0 of the channel tube 170, the inner diameter D 4 at the portion of the channel tube 170 in contact with the protrusion 103 becomes smaller, and the insertion of the sheath 180 deteriorates. The assembleability for inserting the pressing member 100 is also reduced.
 また、口金150の端部へのシース180のスタックを防止する観点から、口金150の基端側領域152bの端部の内径Dは、チャンネルチューブ170の突起103と接する部分での内径D以上とすることが好ましい。チャンネルチューブ170の突起103と接する部分での内径Dは、押さえ部材100の突起103部分での内径Dと、チャンネルチューブ170の外径Dとの関係等により、チャンネルチューブ170の本来の内径Dと異なるものとなりうるため、当該数値を考慮したうえで内径Dおよび内径Dを設定することが好ましい。なお、チャンネルチューブ170の口金150への固定の際に接着剤を使用する場合には、接着剤の厚みも考慮することが好ましい。  Further, from the viewpoint of preventing the sheath 180 from being stacked on the end portion of the base 150, the inner diameter D 5 of the end portion of the base end side region 152b of the base 150 is the inner diameter D 4 at the portion in contact with the protrusion 103 of the channel tube 170. The above is preferable. The inner diameter D 4 at the portion of the channel tube 170 in contact with the protrusion 103 is the original diameter of the channel tube 170 due to the relationship between the inner diameter D 3 of the protrusion 103 of the pressing member 100 and the outer diameter D 0 of the channel tube 170. Since it may be different from the inner diameter D 1 , it is preferable to set the inner diameter D 5 and the inner diameter D 4 in consideration of the relevant values. When an adhesive is used when fixing the channel tube 170 to the base 150, it is preferable to consider the thickness of the adhesive.
 一方、押さえ部材100の第1本体部101の内径Dは、口金150の基端側領域152bを被覆したチャンネルチューブ170の外径Dと同程度であることが好ましい。第1本体部101の内径Dが、チャンネルチューブ170の外径Dより大きいと、チャンネルチューブ170と押さえ部材100との間に隙間が生じるため、押さえ部材100が口金150から偏心したり、傾いて組み付いたりするおそれがある。係る場合、押さえ部材100によるチャンネルチューブ170の保持がうまくいかず、シース180の挿通不良が生じる場合がある。また、第1本体部101の内径Dが、チャンネルチューブ170の外径Dより小さいと、押さえ部材100を口金150に組み付ける際に、チャンネルチューブ170を圧縮する必要があり、組み付けが困難となる。 On the other hand, it is preferable that the inner diameter D 6 of the first main body portion 101 of the pressing member 100 is about the same as the outer diameter D 7 of the channel tube 170 covering the base end side region 152b of the base 150. If the inner diameter D 6 of the first main body 101 is larger than the outer diameter D 7 of the channel tube 170, a gap is generated between the channel tube 170 and the holding member 100, so that the holding member 100 is eccentric from the base 150. There is a risk of tilting and assembling. In such a case, the holding of the channel tube 170 by the pressing member 100 may not be successful, resulting in poor insertion of the sheath 180. Further, if the inner diameter D 6 of the first main body portion 101 is smaller than the outer diameter D 7 of the channel tube 170, it is necessary to compress the channel tube 170 when assembling the holding member 100 to the base 150, which makes assembly difficult. Become.
 さらに、押さえ部材100の第1本体部101の内径Dと、口金150の基端側領域152bの外径Dとの差は、自然状態でのチャンネルチューブ170の肉厚tの2倍以下であることが好ましい。 Further, the difference between the inner diameter D 6 of the first main body portion 101 of the pressing member 100 and the outer diameter D 8 of the base end side region 152b of the base 150 is not more than twice the wall thickness t of the channel tube 170 in the natural state. Is preferable.
 図7は、図2の超音波内視鏡2の湾曲部212の湾曲を説明する図である。湾曲部212は、図示しない複数の湾曲駒を連結して構成され、湾曲ノブ221(図1参照)を操作することにより、上下および左右方向に湾曲する。従来、湾曲部は、同一形状の湾曲駒を複数連結して構成されているが、本発明の超音波内視鏡2の湾曲部212は、先端側に配置される湾曲駒の間隔が、基端側に配置される湾曲駒の間隔より小さくなるものを使用する。図7に示すように、湾曲ノブ221の操作により湾曲部212を湾曲させる場合、まず、先端側に配置される湾曲駒の湾曲方向の間隔が縮まることで湾曲部212の先端側のみが湾曲し(図7(b)参照)、さらに湾曲ノブ221が操作されると、配置された順に先端側から基端側の湾曲駒の間隔が縮まって、湾曲部212の全体が湾曲する(図7(c)参照)。 FIG. 7 is a diagram illustrating the curvature of the curved portion 212 of the ultrasonic endoscope 2 of FIG. The curved portion 212 is configured by connecting a plurality of curved pieces (not shown), and is curved in the vertical and horizontal directions by operating the curved knob 221 (see FIG. 1). Conventionally, the curved portion is configured by connecting a plurality of curved pieces having the same shape, but in the curved portion 212 of the ultrasonic endoscope 2 of the present invention, the distance between the curved pieces arranged on the tip side is the base end. Use one that is smaller than the distance between the curved pieces placed on the side. As shown in FIG. 7, when bending the bending portion 212 by operating the bending knob 221, first, only the tip side of the bending portion 212 is curved by shortening the interval in the bending direction of the bending pieces arranged on the tip side ( 7 (b)) Further, when the bending knob 221 is operated, the distance between the bending pieces from the tip end side to the base end side is shortened in the order in which they are arranged, and the entire bending portion 212 is curved (FIG. 7 (c)). reference).
 近年、従来のものより湾曲部212の短小化、細径化、および湾曲角度が増大された超音波内視鏡2が使用され、例えば、湾曲部212の径は15mm程度であったものが13mm程度に、湾曲部212の長さは従来のものが50mm程度であったものが40mm程度に、最大湾曲角度は従来のものが90°程度であったものがから130°以上、さらには150°以上程度に変更された超音波内視鏡2が使用されるようになっている。湾曲部212の長さを短くし、湾曲角度を大きくすると、湾曲させた状態での隣接する湾曲駒間のなす角度も大幅に上昇する。さらに、湾曲部212の細径化も加わり、湾曲角度が小さい状態でも押さえ部材100の端部へのシース180の先端部の引っかかりが発生しやすくなっていた。本発明では、先端側に配置される湾曲駒の間隔を、基端側に配置される湾曲駒の間隔より小さくすることにより、湾曲させた状態での隣接する湾曲駒間のなす角度が小さくなるため、押さえ部材100の端部へのシース180の先端部の引っかかりを防止することができる。 In recent years, an ultrasonic endoscope 2 having a shorter curved portion, a smaller diameter, and an increased bending angle has been used as compared with the conventional one. For example, the diameter of the curved portion 212 is about 15 mm, which is 13 mm. The length of the curved portion 212 is about 40 mm in the conventional one, which was about 50 mm, and the maximum bending angle is 130 ° or more, and further 150 ° from the one in which the conventional one was about 90 °. The ultrasonic endoscope 2 modified to the above degree has come to be used. When the length of the curved portion 212 is shortened and the curved angle is increased, the angle formed between the adjacent curved pieces in the curved state is also significantly increased. Further, the diameter of the curved portion 212 has been reduced, and even when the bending angle is small, the tip portion of the sheath 180 is likely to be caught on the end portion of the pressing member 100. In the present invention, by making the distance between the curved pieces arranged on the tip side smaller than the distance between the curved pieces arranged on the base end side, the angle formed between the adjacent curved pieces in the curved state becomes smaller. It is possible to prevent the tip portion of the sheath 180 from being caught on the end portion of the pressing member 100.
 また、湾曲部212の細径化に伴い、超音波モジュール214や撮像モジュール215への電源供給および各種信号を伝送する複数の信号ケーブルも細径化されるが、細径化により弾性に乏しいケーブル構造体となることがある。かかる信号ケーブルは、短小化、湾曲角度が増大した湾曲部212の湾曲操作により、座屈して断線するおそれが高くなる。信号ケーブルの断線防止の観点から、湾曲部212内に配置される信号ケーブルの周囲を、湾曲は可能であるが硬質な熱収縮チューブによって被覆することが好ましい。 Further, as the diameter of the curved portion 212 is reduced, the diameter of a plurality of signal cables for supplying power to the ultrasonic module 214 and the image pickup module 215 and transmitting various signals is also reduced, but the cable is less elastic due to the reduction in diameter. It may be a structure. Such a signal cable is more likely to buckle and break due to the bending operation of the bending portion 212 which is shortened and the bending angle is increased. From the viewpoint of preventing disconnection of the signal cable, it is preferable to cover the periphery of the signal cable arranged in the curved portion 212 with a heat-shrinkable tube that can be curved but is hard.
(変形例1)
 図8は、本発明の実施の形態に係る内視鏡の変形例1を説明する上面図であり、図9は、図8の断面図である。変形例1に係る押さえ部材100Aは、外表面に取付位置を示す指標を有する。
(Modification 1)
FIG. 8 is a top view illustrating a modification 1 of the endoscope according to the embodiment of the present invention, and FIG. 9 is a cross-sectional view of FIG. The holding member 100A according to the first modification has an index indicating the mounting position on the outer surface.
 押さえ部材100Aは、第1本体部101Aと、第2本体部102と、を有し、第2本体部102Aは第1本体部より外径が太径に構成されている。押さえ部材100Aでは、第1本体部101Aと第2本体部102Aとの境界線が、押さえ部材100Aの取り付け位置を示す指標となる。 The pressing member 100A has a first main body portion 101A and a second main body portion 102, and the second main body portion 102A is configured to have a larger outer diameter than the first main body portion. In the pressing member 100A, the boundary line between the first main body portion 101A and the second main body portion 102A serves as an index indicating the mounting position of the pressing member 100A.
 押さえ部材100Aは、指標、すなわち第1本体部101Aと第2本体部102Aを横断した切り欠き106を有する。切り欠き106は、図8に示すように、押さえ部材106Aの外表面から内表面まで貫通する切り欠きである。押さえ部材100Aを、チャンネルチューブ170を被せた口金150の基端側領域152bに組み付ける際、切り欠き106から透明なチャンネルチューブ170を通して見える基端側領域152bの基端を確認し、基端と指標とを一致、または指標が基端より先端側に位置するように押さえ部材100Aを組み付ける。これにより、押さえ部材100Aを口金150に正確な位置に容易に取り付け可能となる。なお、変形例1では、第1本体部101Aと第2本体部102Aを異なる外径として指標としたが、指標はこれに限定するものではない。指標は、同径に形成した第1本体部と第2本体部の境界に、レーザ等による溝や、印刷等で指標を形成してもよい。また、切り欠き106は、切り欠き106へのシース180の先端部の引っかかりを防止するために、最も湾曲角度が大きいUP側に配置することが好ましい。 The pressing member 100A has an index, that is, a notch 106 that crosses the first main body portion 101A and the second main body portion 102A. As shown in FIG. 8, the notch 106 is a notch that penetrates from the outer surface to the inner surface of the pressing member 106A. When the pressing member 100A is assembled to the proximal end side region 152b of the base 150 covered with the channel tube 170, the proximal end side region 152b visible through the transparent channel tube 170 from the notch 106 is confirmed, and the proximal end and the index are confirmed. Assemble the pressing member 100A so that the index is located on the tip side from the base end. This makes it possible to easily attach the holding member 100A to the base 150 at an accurate position. In the first modification, the first main body portion 101A and the second main body portion 102A are used as indexes as different outer diameters, but the index is not limited to this. As the index, a groove formed by a laser or the like or an index may be formed by printing or the like at the boundary between the first main body portion and the second main body portion formed to have the same diameter. Further, the notch 106 is preferably arranged on the UP side having the largest bending angle in order to prevent the tip portion of the sheath 180 from being caught in the notch 106.
(変形例2)
 図10は、本発明の実施の形態に係る内視鏡の変形例2を説明する上面図である。変形例2に係る押さえ部材100Bは、変形例1と同様に外表面に取付位置を示す指標を有する。押さえ部材100Bでは、指標、すなわち第1本体部101Bと第2本体部102Bを横断した切り欠き106Bを有し、切り欠き106Bは、第2本体部102Bの基端側まで設けられている。第2本体部102Bの基端側まで切り欠き106Bを設けることにより、チャンネルチューブ170の取り換え時等に押さえ部材100Bの取り外しを容易に行うことができる。
(Modification 2)
FIG. 10 is a top view illustrating a modification 2 of the endoscope according to the embodiment of the present invention. The holding member 100B according to the modified example 2 has an index indicating the mounting position on the outer surface as in the modified example 1. The pressing member 100B has an index, that is, a notch 106B that crosses the first main body portion 101B and the second main body portion 102B, and the notch 106B is provided up to the base end side of the second main body portion 102B. By providing the notch 106B up to the base end side of the second main body portion 102B, the pressing member 100B can be easily removed when the channel tube 170 is replaced or the like.
(変形例3)
 図11は、本発明の実施の形態に係る内視鏡の変形例3を説明する上面図である。変形例2に係る押さえ部材100Dは、第1本体部101Dと第2本体部102Dは外径が同径に形成され、第2本体部102Dに切り欠き106Dが配置されている。切り欠き106Dの第1本体部101D側の端部が、第1本体部101Dと第2本体部102Dとの境界に一致するように切り欠き106Dを形成している。変形例3では、切り欠き106Dの第1本体部101D側の端部が指標となる。
(Modification 3)
FIG. 11 is a top view illustrating a modified example 3 of the endoscope according to the embodiment of the present invention. In the holding member 100D according to the second modification, the first main body portion 101D and the second main body portion 102D are formed to have the same outer diameter, and the notch 106D is arranged in the second main body portion 102D. The notch 106D is formed so that the end portion of the notch 106D on the first main body portion 101D side coincides with the boundary between the first main body portion 101D and the second main body portion 102D. In the third modification, the end portion of the notch 106D on the first main body portion 101D side serves as an index.
(変形例4)
 図12は、本発明の実施の形態に係る内視鏡の変形例4を説明する長手軸方向の断面図である。変形例4では、口金150Eは、チャンネルチューブ170や押さえ部材100Eの端部と接触するための突き当てる突き当て面155を有する。
(Modification example 4)
FIG. 12 is a sectional view taken along the longitudinal axis for explaining a modification 4 of the endoscope according to the embodiment of the present invention. In the fourth modification, the base 150E has an abutting surface 155 for contacting the end of the channel tube 170 and the pressing member 100E.
 口金150Eは、第1口金部151Eの第2口金部152E側の端部に、チャンネルチューブ170および押さえ部材100Eの端部を突き当てる突き当て面155を有する。突き当て面155は、長手軸方向と直交する面である。 The base 150E has an abutting surface 155 for abutting the end portions of the channel tube 170 and the pressing member 100E at the end portion of the first base portion 151E on the second base portion 152E side. The abutting surface 155 is a surface orthogonal to the longitudinal axis direction.
 押さえ部材100Eの第1本体部101Eは、第2口金部152Eの全体を押圧可能な長さに形成されている。変形例4では、口金150Eと押さえ部材100Eとが重なる領域が大きいため、押さえ部材100Eの口金150Eに対する組付けをより正確に行うことができ、チャンネルチューブ170が負荷を受けた際の押さえ部材100Eの傾きを防止することができる。 The first main body portion 101E of the pressing member 100E is formed to have a length that allows the entire second base portion 152E to be pressed. In the fourth modification, since the area where the base 150E and the holding member 100E overlap is large, the holding member 100E can be assembled more accurately to the base 150E, and the holding member 100E when the channel tube 170 receives a load can be performed more accurately. Can be prevented from tilting.
 さらなる効果や変形例は、当業者によって容易に導き出すことができる。よって、本発明のより広範な態様は、以上のように表し、かつ記述した特定の詳細及び代表的な実施の形態に限定されるものではない。従って、添付のクレーム及びその均等物によって定義される総括的な発明の概念の精神又は範囲から逸脱することなく、様々な変更が可能である。 Further effects and variations can be easily derived by those skilled in the art. Thus, the broader aspects of the invention are not limited to the particular details and representative embodiments described as described above. Thus, various modifications can be made without departing from the spirit or scope of the overall concept of the invention as defined by the attached claims and their equivalents.
 1 内視鏡システム
 2 超音波内視鏡
 3 超音波観測装置
 4 内視鏡観察装置
 5 表示装置
 6 光源装置
 7 超音波振動子
 21 挿入部
 22 操作部
 23 ユニバーサルコード
 24 コネクタ
 31 超音波ケーブル
 41 ビデオケーブル
 61 光ファイバケーブル
 100 押さえ部材
 101 第1本体部
 102 第2本体部
 103 突起
 105 テーパ面
 106 切り欠き
 150 口金
 151 第1口金部
 152 第2口金部
 153、154、171、220 貫通孔
 155 突き当て面
 170 チャンネルチューブ
 180 シース
 211 先端部
 212 湾曲部
 213 可撓管部
 214 超音波振動子モジュール
 215 内視鏡モジュール
 221 湾曲ノブ
 222 操作部材
 223 処置具挿入口
 224 処置具突入口
 225 ビス
1 Endoscopic system 2 Ultrasonic endoscope 3 Ultrasonic observation device 4 Endoscopic observation device 5 Display device 6 Light source device 7 Ultrasonic oscillator 21 Insertion part 22 Operation part 23 Universal cord 24 Connector 31 Ultrasonic cable 41 Video Cable 61 Optical fiber cable 100 Holding member 101 1st main body 102 2nd main body 103 Protrusion 105 Tapered surface 106 Notch 150 Base 151 1st base 152 2nd base 153, 154, 171, 220 Through hole 155 Butt Surface 170 Channel tube 180 Sheath 211 Tip part 212 Curved part 213 Flexible tube part 214 Ultrasonic transducer module 215 Endoscopic ultrasound module 221 Curved knob 222 Operation member 223 Treatment tool insertion port 224 Treatment tool entrance 225 Screw

Claims (8)

  1.  被検体内に挿入され先端側に先端部材を有する挿入部の長手方向の先端側と基端側とを連通し、処置具を挿通するチャンネルチューブと、
     先端側が前記先端部材の開口の基端側に篏合され、基端側が前記チャンネルチューブに被覆され、前記開口および前記チャンネルチューブとともに前記処置具の挿通路を構成する貫通孔を有する口金と、
     前記チャンネルチューブにより被覆された前記口金の外周の周囲に配置される第1本体部と、前記口金の基端側よりも前記長手方向に突出して配置される第2本体部とを有する、筒状の押さえ部材と、
     を備え、
     前記押さえ部材の第2本体部の内周には、基端側に延出する前記チャンネルチューブの外径を、前記第1本体部と接する前記チャンネルチューブの外径より小さくするように押圧する突起が形成され、前記突起の基端側は、前記チャンネルチューブの外径が徐々に広がるように案内するテーパ面をなす内視鏡。
    A channel tube that communicates the distal end side and the proximal end side of the insertion portion that is inserted into the subject and has the distal end member on the distal end side in the longitudinal direction and inserts the treatment tool.
    A mouthpiece having a front end side fitted to the base end side of the opening of the tip member, the base end side being covered with the channel tube, and having a through hole forming an insertion passage of the treatment tool together with the opening and the channel tube.
    A tubular portion having a first main body portion arranged around the outer periphery of the mouthpiece covered with the channel tube and a second main body portion arranged so as to project in the longitudinal direction from the base end side of the mouthpiece. Holding member and
    Equipped with
    On the inner circumference of the second main body of the holding member, a protrusion that presses the outer diameter of the channel tube extending toward the proximal end so as to be smaller than the outer diameter of the channel tube in contact with the first main body. Is formed, and the base end side of the protrusion is an endoscope having a tapered surface that guides the outer diameter of the channel tube to gradually expand.
  2.  前記押さえ部材は、前記第1本体部と前記第2本体部とを接合してなる請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein the holding member is formed by joining the first main body portion and the second main body portion.
  3.  前記押さえ部材の外表面に、前記口金との取付位置を示す指標が配設されている請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein an index indicating a mounting position with the mouthpiece is arranged on the outer surface of the holding member.
  4.  前記押さえ部材は、前記指標を横断した切り欠きを有する請求項3に記載の内視鏡。 The endoscope according to claim 3, wherein the holding member has a notch across the index.
  5.  前記第1本体部の内径と前記口金の基端側の外径との差は、自然状態での前記チャンネルチューブの肉厚の2倍以下である請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein the difference between the inner diameter of the first main body and the outer diameter of the base end side of the base is not more than twice the wall thickness of the channel tube in a natural state.
  6.  前記口金は、前記チャンネルチューブと接触するための突き当て面を有する請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein the mouthpiece has an abutting surface for contacting with the channel tube.
  7.  湾曲部の最大湾曲角度が130°以上である請求項1に記載の内視鏡。 The endoscope according to claim 1, wherein the maximum bending angle of the curved portion is 130 ° or more.
  8.  前記湾曲部は複数の湾曲駒を連結して構成され、先端側に配置される湾曲駒の間隔は、基端側に配置される湾曲駒の間隔より小さい請求項7に記載の内視鏡。 The endoscope according to claim 7, wherein the curved portion is configured by connecting a plurality of curved pieces, and the distance between the curved pieces arranged on the tip end side is smaller than the distance between the curved pieces arranged on the proximal end side.
PCT/JP2020/023995 2020-06-18 2020-06-18 Endoscope WO2021255903A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/JP2020/023995 WO2021255903A1 (en) 2020-06-18 2020-06-18 Endoscope

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2020/023995 WO2021255903A1 (en) 2020-06-18 2020-06-18 Endoscope

Publications (1)

Publication Number Publication Date
WO2021255903A1 true WO2021255903A1 (en) 2021-12-23

Family

ID=79267685

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2020/023995 WO2021255903A1 (en) 2020-06-18 2020-06-18 Endoscope

Country Status (1)

Country Link
WO (1) WO2021255903A1 (en)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56163405U (en) * 1980-05-09 1981-12-04
JPH02271817A (en) * 1990-03-06 1990-11-06 Olympus Optical Co Ltd Endoscope
JPH09253033A (en) * 1996-03-25 1997-09-30 Fuji Photo Optical Co Ltd Treating tool insertion channel for endoscope
JP2002209829A (en) * 2001-01-22 2002-07-30 Fuji Photo Optical Co Ltd Pipeline connecting structure of endoscope
JP2006218231A (en) * 2005-02-14 2006-08-24 Olympus Corp Flexible tube for endoscope and endoscope
JP2017086399A (en) * 2015-11-09 2017-05-25 富士フイルム株式会社 Endoscope
JP2018117872A (en) * 2017-01-25 2018-08-02 富士フイルム株式会社 Distal part structure of endoscope insertion section and endoscope
JP2018134276A (en) * 2017-02-22 2018-08-30 富士フイルム株式会社 Treatment instrument channel and endoscope

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56163405U (en) * 1980-05-09 1981-12-04
JPH02271817A (en) * 1990-03-06 1990-11-06 Olympus Optical Co Ltd Endoscope
JPH09253033A (en) * 1996-03-25 1997-09-30 Fuji Photo Optical Co Ltd Treating tool insertion channel for endoscope
JP2002209829A (en) * 2001-01-22 2002-07-30 Fuji Photo Optical Co Ltd Pipeline connecting structure of endoscope
JP2006218231A (en) * 2005-02-14 2006-08-24 Olympus Corp Flexible tube for endoscope and endoscope
JP2017086399A (en) * 2015-11-09 2017-05-25 富士フイルム株式会社 Endoscope
JP2018117872A (en) * 2017-01-25 2018-08-02 富士フイルム株式会社 Distal part structure of endoscope insertion section and endoscope
JP2018134276A (en) * 2017-02-22 2018-08-30 富士フイルム株式会社 Treatment instrument channel and endoscope

Similar Documents

Publication Publication Date Title
US7488288B2 (en) Ultrasonic endoscope
US6514210B2 (en) Forward viewing and radial scanning ultrasonic endoscope
JP4618410B2 (en) Ultrasound endoscope
JP2004135937A (en) Ultrasonic endoscope
US20200107708A1 (en) Endoscope
US11903758B2 (en) Ultrasonic endoscope
US10869649B2 (en) Ultrasound transducer module and ultrasound endoscope
JP4484044B2 (en) Ultrasound endoscope
WO2021255903A1 (en) Endoscope
JP4017925B2 (en) Ultrasound endoscope
US20190000417A1 (en) Endoscope
CN107708573B (en) Ultrasonic endoscope
US20180098688A1 (en) Lens unit and endoscope
JP6850694B2 (en) Endoscope and manufacturing method of endoscope
JP6744118B2 (en) Endoscope
JP2017074231A (en) Method of manufacturing ultrasonic endoscope and ultrasonic endoscope
US11944496B2 (en) Ultrasound endoscope
US20230119963A1 (en) Ultrasound endoscope and method of manufacturing ultrasound endoscope
US11076744B2 (en) Method of manufacturing endoscope and endoscope
WO2021181705A1 (en) Endoscope
JP7219580B2 (en) Ultrasonic endoscope and method for manufacturing ultrasonic endoscope
JP4488203B2 (en) Ultrasound endoscope
JP2023128309A (en) Endoscope
JP2017225746A (en) Endoscope
JPWO2017150461A1 (en) Ultrasound endoscope and method for manufacturing ultrasound endoscope

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20941098

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 20941098

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: JP