CN115661132A - Computer storage medium and device for detecting benign and malignant pulmonary nodules - Google Patents

Computer storage medium and device for detecting benign and malignant pulmonary nodules Download PDF

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CN115661132A
CN115661132A CN202211552686.6A CN202211552686A CN115661132A CN 115661132 A CN115661132 A CN 115661132A CN 202211552686 A CN202211552686 A CN 202211552686A CN 115661132 A CN115661132 A CN 115661132A
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lung
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nodule
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汪洋
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Luzhou Vocational and Technical College
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Abstract

The present invention relates to the field of medical imaging techniques, and provides a computer storage medium having program instructions embodied therein for detecting benign and malignant lung nodules for causing a corresponding processor to perform the steps of: acquiring CT images of the known benign and malignant condition of the pulmonary nodule and the benign and malignant condition of the pulmonary nodule to be detected; after the lung nodule characteristic vectors in the lung CT image are set, corresponding lung nodule characteristic vectors in the CT image of the known benign and malignant condition of the lung nodule and the benign and malignant condition of the lung nodule to be detected are respectively extracted; performing clustering analysis on the lung nodule characteristic vectors to obtain various clustering results, and generating a reference clustering data set through the various clustering results; and detecting the benign and malignant condition of the pulmonary nodule to be detected by using the reference cluster data set. The invention provides accurate quantitative analysis for doctors through the quantitative processing technology of images, thereby improving the repeatability of the diagnosis result of the doctors and the consistency of the image and the disease explanation to a certain extent, and improving the accuracy and the efficiency of the diagnosis of the doctor.

Description

Computer storage medium and device for detecting benign and malignant pulmonary nodules
Technical Field
The present application relates to the field of medical imaging technologies, and in particular, to a computer storage medium and an apparatus for detecting benign and malignant pulmonary nodules.
Background
The discrimination and diagnosis of the benign and malignant lung nodules is the key for realizing the early diagnosis of the lung cancer. CT is considered as the best medical imaging means for examining lung diseases, but CT belongs to three-dimensional tomographic images, and has a large amount of image data, especially HRCT (High Resolution three-dimensional tomographic image), the amount of image data is increased sharply compared with the amount of data in a common CT image set, generally, one whole lung HRCT includes 200 to 500 scanned images, or even more, so that in a large-scale lung disease screening process, radiologists face a large number of CT images, and missed diagnosis and misdiagnosis of diseases are easily caused by diagnosis fatigue. Therefore, a computer aided diagnosis system for detecting benign and malignant lung nodules is needed to effectively assist a doctor in diagnosing benign and malignant lung nodules with suspicious lesions through a large number of lung CT images.
Disclosure of Invention
In view of the deficiencies in the prior art and the needs of practical applications, the present invention provides, in a first aspect, a computer storage medium for detecting benign and malignant lung nodules, the computer storage medium storing a computer program comprising program instructions that, when executed by a processor, cause the processor to perform the steps of: acquiring lung electron computer tomography images of known benign and malignant pulmonary nodules and benign and malignant pulmonary nodules to be detected; setting a lung nodule characteristic vector in a lung electron computed tomography image; extracting a first pulmonary nodule feature vector in a pulmonary electron computed tomography image of a known benign and malignant condition of a pulmonary nodule; obtaining a plurality of clustering results through the first lung nodule feature vector, and generating a reference clustering data set through the plurality of clustering results; extracting a second pulmonary nodule feature vector in the pulmonary electron computed tomography image of the benign and malignant condition of the pulmonary nodule to be detected; and detecting benign lung nodules and malignant lung nodules in the lung electron computed tomography image of the benign and malignant condition of the lung nodules to be detected by utilizing the second lung nodule feature vector and combining the reference cluster data set. The method extracts a plurality of characteristic vectors of a lung electron computed tomography image of the known benign and malignant condition of the lung nodule, generates a reference cluster data set for judging the benign and malignant condition of the lung nodule after cluster analysis, and identifies the extracted second lung nodule characteristic vector and diagnoses the benign and malignant condition of the lung nodule to be detected by using the reference cluster data set. The invention provides accurate quantitative analysis for doctors through the image quantization technology, overcomes the defects of inertia of human eyes and insensitivity to gray level, and can reduce the adverse effect of subjective factors of doctors on film reading results, thereby improving the repeatability of the diagnosis results of the doctors and the consistency of image and disease interpretation to a certain extent, and simultaneously reducing the omission of visual observation in the independent film reading diagnosis process of the doctors and the workload of film reading, thereby improving the accuracy and efficiency of the doctor diagnosis of the state of illness.
Optionally, the setting of the feature vector of the lung nodule in the lung electron computed tomography image includes the following steps: setting two-dimensional feature vectors in a single-layer lung electron computed tomography image, wherein the two-dimensional feature vectors comprise two-dimensional morphological feature vectors, two-dimensional gray-scale feature vectors and two-dimensional gradient feature vectors; and superposing a plurality of single-layer lung electron computed tomography images to form a lung nodule three-dimensional image, and setting a three-dimensional characteristic vector of the lung nodule three-dimensional image, wherein the three-dimensional characteristic vector comprises a three-dimensional morphological characteristic vector, a three-dimensional gray characteristic vector and a three-dimensional ladder characteristic vector.
Optionally, the three-dimensional grayscale feature vector includes a contrast-wise grayscale feature vector, the contrast-wise grayscale feature vector including:
Figure 44094DEST_PATH_IMAGE001
Figure 430076DEST_PATH_IMAGE002
Figure 803289DEST_PATH_IMAGE003
wherein, inside represents the inner region of the three-dimensional lung nodule,
Figure 401760DEST_PATH_IMAGE004
,outsideI represents the expanded peripheral region of the three-dimensional lung nodule,
Figure 809608DEST_PATH_IMAGE005
and
Figure 100912DEST_PATH_IMAGE006
represent the same class of features within the insert and outcidel regions respectively,
Figure 961421DEST_PATH_IMAGE008
and
Figure 425900DEST_PATH_IMAGE009
indicate the standard deviation corresponding to the same class of features in the inner and outer idei regions, respectively.
Optionally, the three-dimensional gradient feature vector comprises components of the gradient feature vector on three-dimensional coordinate axes, the components
Figure 563620DEST_PATH_IMAGE010
The following formula is satisfied:
Figure 884880DEST_PATH_IMAGE011
wherein, the first and the second end of the pipe are connected with each other,
Figure 108051DEST_PATH_IMAGE012
Figure 438538DEST_PATH_IMAGE013
representing the components of the three-dimensional gradient feature vector on the X-axis,
Figure 227503DEST_PATH_IMAGE014
representing the component of the three-dimensional gradient feature vector on the Y-axis,
Figure 126189DEST_PATH_IMAGE015
representing the component of the three-dimensional gradient feature vector in the Z-axis,
Figure 695710DEST_PATH_IMAGE016
the gray value of the pixel point with the number i in the square field pixel of the central pixel point of the three-dimensional ladder characteristic vector is represented,
Figure 439675DEST_PATH_IMAGE017
representing the weight of the pixel point numbered i,
Figure 676622DEST_PATH_IMAGE018
in which
Figure 480630DEST_PATH_IMAGE019
Figure 475130DEST_PATH_IMAGE020
Figure 147420DEST_PATH_IMAGE021
Representing the coordinates of a central pixel point
Figure 848660DEST_PATH_IMAGE022
To the pixel point coordinate with number i
Figure 213782DEST_PATH_IMAGE023
The euclidean distance between them.
Optionally, the obtaining multiple kinds of clustering results through the first lung nodule feature vector, and generating a reference clustering data set through the multiple kinds of clustering results includes the following steps: carrying out clustering analysis on the first lung nodule characteristic vector by utilizing different clustering algorithms to obtain various clustering results; or carrying out clustering analysis on the first lung nodule characteristic vector through the same clustering algorithm with different parameters and different initial values to obtain a plurality of clustering results; and combining the multiple clustering results to obtain a combined result, and carrying out clustering analysis on the combined result to obtain a reference clustering data set.
Further optionally, the different clustering algorithms include a Kmeans clustering method, a HC clustering algorithm, a MeanShift algorithm, and a Kmeans-HC combined clustering algorithm.
Further optionally, the combined result satisfies the following formula:
Figure 633262DEST_PATH_IMAGE024
wherein the content of the first and second substances,
Figure 781347DEST_PATH_IMAGE026
a matrix obtained by combining a plurality of kinds of clustering results is represented,
Figure 727306DEST_PATH_IMAGE027
Figure 873117DEST_PATH_IMAGE028
representation matrix
Figure 904527DEST_PATH_IMAGE029
Middle sample
Figure 793985DEST_PATH_IMAGE030
And samples
Figure 860030DEST_PATH_IMAGE031
The corresponding numerical value at the indicated position is,
Figure 239059DEST_PATH_IMAGE032
Figure 633131DEST_PATH_IMAGE034
representing the total number of clustering results.
Optionally, the detecting benign pulmonary nodules and malignant pulmonary nodules in the lung electrical computed tomography image of the benign and malignant condition of the pulmonary nodules to be detected by using the second lung nodule feature vector in combination with the reference cluster data set includes the following steps:
obtaining pulmonary nodule feature vector x aiming at ith malignant feature subclass in reference cluster data set respectively
Figure 450914DEST_PATH_IMAGE036
Bayes posterior probability of
Figure 715674DEST_PATH_IMAGE037
And the jth benign feature subclass
Figure 593500DEST_PATH_IMAGE038
Bayes posterior probability of
Figure 271606DEST_PATH_IMAGE039
Setting a good/bad judgment boundary
Figure 768446DEST_PATH_IMAGE041
The benign-malignant determination boundary satisfies the following equation:
Figure 549364DEST_PATH_IMAGE042
converting the good and malignant judgment boundary formula into a Markov space linear judgment equation;
obtaining a Bayesian posterior probability of the second pulmonary nodule feature vector
Figure 942299DEST_PATH_IMAGE037
And Bayes posterior probability
Figure 435597DEST_PATH_IMAGE039
And preliminarily judging the benign and malignant degree of the second lung nodule feature vector according to a benign and malignant degree judgment boundary formula, wherein the benign and malignant degree judgment satisfies the following formula:
Figure 267287DEST_PATH_IMAGE043
respectively calculating the second lung nodule feature vector to the jth benign feature subclass
Figure 37797DEST_PATH_IMAGE045
Mahalanobis distance of center
Figure 991846DEST_PATH_IMAGE046
And to the ithSubclass of malignancy characteristics
Figure 582228DEST_PATH_IMAGE047
Mahalanobis distance of center
Figure 545504DEST_PATH_IMAGE048
According to the Mahalanobis distance
Figure 904941DEST_PATH_IMAGE050
And said Mahalanobis distance
Figure 967575DEST_PATH_IMAGE052
Combined decision coordinates
Figure 169887DEST_PATH_IMAGE053
At the mahalanobis location, the second lung nodule feature vector is again determined to be benign or malignant: if the second lung nodule feature vector belongs to the benign feature after the primary judgment, the judgment coordinate corresponding to the second lung nodule feature vector
Figure 812221DEST_PATH_IMAGE054
If the second lung nodule feature vector is located below the mahalanobis space linear judgment straight line, the second lung nodule feature vector is false positive; if the second lung nodule feature vector is judged to belong to the malignant feature for the first time, judging coordinates corresponding to the second lung nodule feature vector
Figure 150798DEST_PATH_IMAGE054
If the second pulmonary nodule feature vector is located above the mahalanobis space linear judgment straight line, the second pulmonary nodule feature vector is false negative;
all benign lung nodules are detected when the number of false positive second lung nodule feature vectors is minimum by optimizing mahalanobis space linear decision equation parameters.
Further optionally, the mahalanobis space linear decision equation satisfies the following formula:
Figure 587596DEST_PATH_IMAGE055
wherein, the first and the second end of the pipe are connected with each other,
Figure 277203DEST_PATH_IMAGE057
representing feature vectors x through jth benign feature subclass
Figure 254386DEST_PATH_IMAGE058
The mahalanobis distance of the center of the circle,
Figure 588416DEST_PATH_IMAGE060
representing feature vectors x through the ith malignancy feature subclass
Figure 320748DEST_PATH_IMAGE062
The mahalanobis distance of the center of the circle,
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is the ith malignancy feature subclass
Figure 950630DEST_PATH_IMAGE062
The expansion times of the powder are increased by a plurality of times,
Figure 201482DEST_PATH_IMAGE065
is a linear intercept parameter.
In a second aspect, the present invention also provides an apparatus for detecting benign and malignant lung nodules, comprising a processor, an input device, an output device, and a memory, the processor, the input device, the output device, and the memory being interconnected, the memory including the computer storage medium of the first aspect for detecting benign and malignant lung nodules, the processor being configured to invoke the program instructions. The device for detecting the benign and malignant pulmonary nodules provided by the invention has the advantages of compact structure and stable performance, and can efficiently and accurately execute the program instructions contained in the computer storage medium for detecting the benign and malignant pulmonary nodules in the memory.
Drawings
FIG. 1 is a schematic flow chart of program instructions stored on a computer storage medium for detecting benign and malignant pulmonary nodules according to the present invention;
FIG. 2 is a schematic diagram of an eight-domain pixel in an embodiment of the invention;
FIG. 3 is a schematic diagram of 4 different structural elements in an embodiment of the present invention;
FIG. 4 is a schematic diagram of a square field pixel in an embodiment of the invention;
FIG. 5 is a schematic diagram of a linear decision space in Mahalanobis space in an embodiment of the present invention;
fig. 6 is a schematic structural diagram of the device for detecting benign and malignant pulmonary nodules according to the present invention.
Detailed Description
Specific embodiments of the present invention will be described in detail below, and it should be noted that the embodiments described herein are merely illustrative and are not intended to limit the present invention. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present invention. However, it will be apparent to one of ordinary skill in the art that: it is not necessary to employ these specific details to practice the present invention. In other instances, well-known circuits, software, or methods have not been described in detail in order to avoid obscuring the present invention.
Throughout the specification, reference to "one embodiment," "an embodiment," "one example" or "an example" means: the particular features, structures, or characteristics described in connection with the embodiment or example are included in at least one embodiment of the invention. Thus, the appearances of the phrases "in one embodiment," "in an embodiment," "one example" or "an example" in various places throughout this specification are not necessarily all referring to the same embodiment or example. Furthermore, the particular features, structures, or characteristics may be combined in any suitable combination and/or sub-combination in one or more embodiments or examples. Further, those of ordinary skill in the art will appreciate that the illustrations provided herein are for illustrative purposes and are not necessarily drawn to scale.
CT is considered as the best medical imaging means for examining lung diseases, but belongs to three-dimensional tomographic images, the amount of image data is large, especially HRCT (High Resolution computed tomography), the image data amount is rapidly increasing, and generally, one whole lung HRCT contains 200 to 500 scan images, or even more. The present invention is based on the insight that a large number of CT images of the lung assist a physician in intelligently identifying and diagnosing lung nodules in the early stages of lung cancer, and for its objects, features and advantages, it is further described in the following examples.
Referring to fig. 1, in one embodiment, the present invention provides a computer storage medium for detecting the malignancy and/or malignancy of a lung nodule, the computer storage medium storing a computer program comprising program instructions that, when executed by a processor, cause the processor to perform the steps of:
s01, acquiring lung electronic computed tomography images of known benign and malignant pulmonary nodules and pulmonary nodule benign and malignant pulmonary nodule conditions to be detected.
The pulmonary electron computed tomography images of the benign and malignant condition of a known lung nodule can be acquired by a hospital PACS (Picture Archiving and Communication System). The lung electron computer tomography image of the benign and malignant condition of the lung nodule to be detected can be acquired by a patient of the condition of the lung nodule to be detected by CT image acquisition in a hospital.
S02, lung nodule feature vectors in the lung electron computed tomography image are set.
In an alternative embodiment, the setting of the lung nodule feature vector in the lung electron computed tomography image in step S02 includes the following steps: setting two-dimensional feature vectors in a single-layer lung electron computed tomography image, wherein the two-dimensional feature vectors comprise two-dimensional morphological feature vectors, two-dimensional gray-scale feature vectors and two-dimensional gradient feature vectors; and superposing a plurality of single-layer lung electron computed tomography images to form a lung nodule three-dimensional image, and setting a three-dimensional characteristic vector of the lung nodule three-dimensional image, wherein the three-dimensional characteristic vector comprises a three-dimensional morphological characteristic vector, a three-dimensional gray characteristic vector and a three-dimensional ladder characteristic vector.
In this embodiment, for a two-dimensional morphological feature vector, a two-dimensional grayscale feature vector, and a two-dimensional gradient feature vector included in a two-dimensional feature vector, the two-dimensional grayscale feature vector and the two-dimensional gradient feature vector are further divided into an inner feature (inside), an expanded outer feature (outside), and a Separation feature for comparing the inside and the outside, respectively, according to a position feature.
Wherein the two-dimensional morphological feature vector comprises Size, area, circulation, eccentricity, compact, square compact, distance to center of current magnitude, distance to volume property, juxtapleural, fraction measuring magnitude, orientation X, orientation Y, X-Fraction, Y-Fraction, X-Fraction2 and Y-Fraction2. The Size represents the one-dimensional Size measurement of the lung nodule and is defined as the circular area with the diameter of the maximum distance between any two pixel points of the lung nodule boundary segmented from the lung electron computed tomography image; area represents the Area of a lung nodule region and is defined as the Area of each pixel point in a lung nodule image segmented from a lung electron computed tomography image multiplied by the number of the pixel points; circulation represents the roundness of the pulmonary nodule, and is defined as taking a circle with the area equal to the area of the pulmonary nodule area, taking the center of the circle to all pixel points in the pulmonary nodule area, calculating the number of the pixel points in the pulmonary nodule area in the circle, and dividing the maximum value of the number of the pixel points by the area of each pixel point; eccentricity represents Eccentricity, defined as the ratio of the maximum diameter of the lung nodule region perpendicular to the maximum diameter; compactness, defined as the area of the lung nodule region divided by the area of a circle of equal circumference; square Compactness represents Square Compactness and is defined as the area of a lung nodule region divided by the area surrounded by the minimum Square boundary of the lung nodule region; distance to Center of Current Lung represents the Euclidean Distance between the Center of the Lung nodule region and the Center of the bounding box of the Lung in the Current CT image where it is located; the Distance to lung perimeter represents the minimum value of the Euclidean Distance between the center of the lung nodule area and the half lung boundary pixel where the lung nodule area is located; juxtapleural indicates whether the lung nodule region is in contact with the lung boundary, juxtapleura is a Boolean feature; the Fraction touching lung nodule region represents the degree of contact of the lung nodule region with the lung boundary, defined as the number of pixels in contact with the lung boundary divided by the total number of its boundary pixels; orientation X represents the angle between the maximum diameter of the lung nodule area and the positive axis of X; origin Y represents the angle between the largest diameter of the lung nodule region and the Y forward axis; the X-Fraction is defined as taking the middle point of the upper boundary of a half lung boundary box where the lung nodule region is as a reference point, and dividing the horizontal distance between the central pixel point of the lung nodule region and the reference point by the horizontal width of the current boundary box; the Y-Fraction is defined as taking the middle point of the upper boundary of the half lung boundary box where the lung nodule area is as a reference point, and dividing the vertical distance between the central pixel point of the lung nodule area and the reference point by the vertical width of the current boundary box; defining X-Fraction2 as a reference point by taking the middle point of the boundary on the whole lung bounding box, and dividing the horizontal distance between the central pixel point of the lung nodule area and the reference point by the horizontal width of the current bounding box; Y-Fraction2 is defined as the vertical distance between the center pixel point of the lung nodule region and the reference point divided by the vertical width of the current bounding box, with the midpoint of the border over the entire lung bounding box as the reference point.
The two-dimensional gray feature vector is to calculate a statistical value of gray values of all pixel points in a two-dimensional region (inside) of the segmented lung nodule, and to calculate a statistical value of gray values of all pixel points in a peripheral region (outside) of the lung nodule through expansion operation aiming at the original segmented lung nodule region. Two-dimensional grayscale feature vectors include Max inside, min inside, mean inside, std definition inside, mean outside, std definition outside, contrast1, contrast2, mean separation, std definition separation, skiew inside, kurtosis inside, and motion 1 to 7 inside. The Max inside represents the maximum value of the gray value of each pixel point in the two-dimensional region of the lung nodule; min inside represents the minimum value of the gray value of each pixel point in the two-dimensional region of the lung nodule; mean inside represents the average value of the gray values of all pixel points in the two-dimensional region of the lung nodule; std definition inside represents the standard deviation of the gray value of each pixel point in the two-dimensional region of the lung nodule; mean outside represents the average value of gray values of all pixel points in the peripheral area of the lung nodule; std definition outside represents each pixel point in peripheral region of pulmonary noduleThe standard deviation of the gray value of (a); contrast1 is defined as
Figure 980083DEST_PATH_IMAGE067
I.e. the mean value of the gray values of the pixels in the two-dimensional region of the lung nodule
Figure 644282DEST_PATH_IMAGE068
Obtained by subtracting Mean outside of the peripheral region of the lung nodule; contrast2 is defined as
Figure 900951DEST_PATH_IMAGE069
I.e. the standard deviation of the gray values of the pixels in the two-dimensional region of the lung nodule
Figure 334207DEST_PATH_IMAGE070
Plus Std clearance outside of the peripheral region of the lung nodule; mean separation is defined as
Figure 80446DEST_PATH_IMAGE071
Dividing the absolute value of the difference of the average values of the gray values of the pixels in the inner and outer regions of the lung nodule by the sum of the average values; std definition setting is defined as
Figure 841728DEST_PATH_IMAGE072
I.e. the absolute value of the difference between the standard deviations of the gray values of the pixels in the inner and outer regions of the lung nodule is divided by the sum of the standard deviations; skew inside represents the statistical characteristic of asymmetric distribution of the pixels of the section of the lung nodule; kurtosis inside represents the statistical characteristic of the Kurtosis of the lung nodule section pixel; moment 1 to 7 inside represent 7 invariant moments of the lung nodule cross-section image, and the 7 invariant moments are firstly proposed by k.m. hu in 1962 to characterize the shape characteristics of the image. Statistical characterization of lung nodule cross-section pixels for the Skew inside and Kurtosis inside: assuming that the total number of N-level gray levels in the two-dimensional region of the lung nodule is N, and h (i) is used for representing the proportion of the number of the ith-level gray level pixels in the total number of the cross-section pixels, the average gray level value of the pixels in the two-dimensional region of the lung nodule is:
Figure 292301DEST_PATH_IMAGE073
skaw insert satisfies the following formula:
Figure 189850DEST_PATH_IMAGE074
kurtosis inside satisfies the following equation:
Figure 434887DEST_PATH_IMAGE075
the characteristic amplitude (gradient magnitude), radial deviation (radial-deviation) and radial gradient (radial-gradient) of the two-dimensional planar gradient feature, and the interior (inside) of the two-dimensional region of the lung nodule, the inner boundary (perimeter) of the two-dimensional region of the lung nodule, the extra region (outer) obtained by morphological dilation operation on the lung nodule, and the outer boundary (perimeter) of the extra region are classified according to the position. The two-dimensional gradient feature vector includes: x gradient mean represents the average value of the X positive direction gradient amplitudes in the two-dimensional region of the lung nodule, Y gradient mean represents the average value of the Y positive direction gradient amplitudes in the two-dimensional region of the lung nodule, and XY gradient mean is defined as
Figure 949045DEST_PATH_IMAGE076
The Gradient magnetic Mean instrument represents the average value of the two-dimensional Gradient amplitudes in the two-dimensional region of the lung nodule, the Gradient magnetic Std removal instrument represents the standard deviation of the two-dimensional Gradient amplitudes in the two-dimensional region of the lung nodule, the Gradient magnetic Mean permeator instrument represents the average value of the two-dimensional Gradient amplitudes in the inner boundary, the Gradient magnetic Std removal permeator instrument represents the standard deviation of the two-dimensional Gradient amplitudes in the inner boundary, the Gradient magnetic Mean outer represents the average value of the two-dimensional Gradient amplitudes in the additional region, the Gradient magnetic Std removal outer represents the standard deviation of the two-dimensional Gradient amplitudes in the additional region, the Gradient magnetic Mean outer represents the average value of the two-dimensional Gradient amplitudes in the additional region, the Gradient magnetic Mean outer represents the standard deviation of the two-dimensional Gradient amplitudes in the outer boundary, the Gradient magnetic Gradient amplitude is defined, the Gradient magnetic Mean outer boundary represents the standard deviation of the two-dimensional Gradient amplitudes in the additional region, and the Gradient outer boundary represents the standard deviation
Figure 609833DEST_PATH_IMAGE077
Gradient magnetic Std removal Separation is defined as
Figure 752101DEST_PATH_IMAGE078
Gradient magnetic Mean Perimeter Separation is defined as
Figure 308985DEST_PATH_IMAGE079
The Gradient magnetic Std determination Perimeter Separation is defined as
Figure 903914DEST_PATH_IMAGE080
Radial deviation Mean represents the Mean of two-dimensional Radial deviations within the two-dimensional region of the pulmonary nodule, radial deviation Std deviation Inside represents the standard deviation of two-dimensional Radial deviations within the two-dimensional region of the pulmonary nodule, radial deviation simulation inner represents the Mean of two-dimensional Radial deviations on the inner boundary, radial deviation Std deviation simulation inner represents the standard deviation of two-dimensional Radial deviations on the inner boundary, radial deviation Mean outer represents the Mean of two-dimensional Radial deviations in the additional region, radial deviation Std deviation outer represents the standard deviation of two-dimensional Radial deviations in the additional region, radial deviation Meeter represents the Mean of two-dimensional Radial deviations on the outer boundary, radial deviation Std deviation simulation outer represents the standard deviation of two-dimensional Radial deviations on the outer boundary, radial deviation is defined as the Mean of two-dimensional Radial deviations on the outer boundary
Figure 571656DEST_PATH_IMAGE081
The Radial definition Std definition Separation is defined as
Figure 240534DEST_PATH_IMAGE082
Radial definition Mean Perimeter Separation is defined as
Figure 92953DEST_PATH_IMAGE083
A Radial definition Std definition Perimeter Separation is defined as
Figure 316124DEST_PATH_IMAGE084
The Radial gradient Mean represents the average of the two-dimensional Radial gradients within the two-dimensional region of the lung nodule, the Radial gradient Mean represents the standard deviation of the two-dimensional Radial gradients within the two-dimensional region of the lung nodule, the Radial gradient Mean represents the average of the two-dimensional Radial gradients on the inner boundary, the Radial gradient Mean represents the standard deviation of the two-dimensional Radial gradients on the inner boundary, the Radial gradient Mean represents the average of the two-dimensional Radial gradients in the additional region, the Radial gradient Mean represents the standard deviation of the two-dimensional Radial gradients in the outer region, the Radial gradient Mean represents the average of the two-dimensional Radial gradients on the outer boundary, the Radial gradient Mean represents the standard deviation of the two-dimensional Radial gradients on the outer boundary, and the Radial gradient is defined as the average of the two-dimensional Radial gradients on the outer boundary
Figure 398610DEST_PATH_IMAGE085
The Radial gradient Std removal Separation is defined as
Figure 390837DEST_PATH_IMAGE086
Radial gradient Mean Perimeter Separation is defined as
Figure 414156DEST_PATH_IMAGE087
And a Radial gradient Std depth Perimeter Separation as
Figure 655782DEST_PATH_IMAGE088
. The two-dimensional plane gradient feature comprises 39 feature vectors, wherein the gradient feature of the two-dimensional plane is a two-dimensional vector which can be decomposed into two directions of X and Y for specific analysis (in the present specification, the X and Y directions are defined based on lung electron computed tomography images), that is, the two-dimensional plane gradient feature G can be expressed as
Figure 665326DEST_PATH_IMAGE089
Ladder for any pixel point to be analyzedThe degree can be determined by first identifying the eight-domain pixels, and calculating with the first and last rows of the eight-domain pixels, as shown in fig. 2, the middle black pixel in fig. 2 is the center pixel, and the surrounding gray pixels are the eight-domain pixels, and the two-dimensional feature vector of the center pixel is determined
Figure 902272DEST_PATH_IMAGE090
The components satisfy the following formula:
Figure 440701DEST_PATH_IMAGE091
wherein, the first and the second end of the pipe are connected with each other,
Figure 763098DEST_PATH_IMAGE092
expressing the gray value of the pixel point with the number i in the eight-domain pixels of the central pixel point,
Figure 310754DEST_PATH_IMAGE093
representing the weight in the gradient calculation of the pixel point with the number i,
Figure 74311DEST_PATH_IMAGE094
in which
Figure 173854DEST_PATH_IMAGE095
Figure 858913DEST_PATH_IMAGE096
Representing the coordinates of a central pixel
Figure 69314DEST_PATH_IMAGE097
To the pixel point coordinate with number i
Figure 890640DEST_PATH_IMAGE098
The euclidean distance between them. For two-dimensional feature vectors of central point pixels
Figure 426664DEST_PATH_IMAGE099
The first and last rows of eight-domain pixels through which a component can pass are computed
Figure 130177DEST_PATH_IMAGE100
The manner of the component is obtained. The feature amplitude (gradient magnitude) of the two-dimensional plane gradient feature G is defined as
Figure 19636DEST_PATH_IMAGE101
(ii) a Radial-deviation (radial-deviation) is expressed as the included angle between the gradient vector on any central pixel point and the radial direction (the radial direction represents the connecting line of the central pixel point and the central point of the pulmonary nodule and points to the central direction of the pulmonary nodule)
Figure 820102DEST_PATH_IMAGE102
(ii) a Radial-gradient (radial-gradient) is expressed as the projection size of the gradient vector of any central pixel point in the radial direction and is defined as
Figure 136814DEST_PATH_IMAGE103
In the embodiment, the lung nodule three-dimensional image is formed by superposing a plurality of single-layer lung electron computed tomography images. Therefore, the three-dimensional feature vector comprises a two-dimensional statistical feature vector besides the three-dimensional feature vector of the three-dimensional feature vector, so that the comprehensiveness of three-dimensional feature extraction is ensured. The three-dimensional gray level feature vector and the three-dimensional gradient feature vector are further distinguished into an internal feature (inside), an expanded external feature (outside) and a Separation feature between the inside and the outside according to the position feature. The statistics of the two-dimensional feature values of the group of single-layer two-dimensional lung computer-scanned images constituting the three-dimensional image of the lung nodule represented by the two-dimensional statistical feature vector in the three-dimensional feature vector specifically include the following feature vectors:
Figure 327623DEST_PATH_IMAGE104
Figure 145407DEST_PATH_IMAGE105
Figure 941324DEST_PATH_IMAGE106
Figure 553571DEST_PATH_IMAGE107
wherein the content of the first and second substances,
Figure 434940DEST_PATH_IMAGE108
representing the number of single-slice two-dimensional electronically computer-scanned images of the lungs that make up the three-dimensional image of the lung nodule,
Figure 462939DEST_PATH_IMAGE109
representing the statistical average of the mean values of the two-dimensional characteristic values of the single-layer two-dimensional lung computer-scanned images constituting the three-dimensional image of the lung nodule,
Figure 237997DEST_PATH_IMAGE110
representing the statistical minimum of the two-dimensional characteristic values of the single-layer two-dimensional lung computer scanning image which forms the three-dimensional image of the lung nodule,
Figure 162090DEST_PATH_IMAGE111
representing the statistical maximum of the two-dimensional characteristic values of the single-layer two-dimensional lung electronic computer scanning image which forms the three-dimensional image of the lung nodule,
Figure 389809DEST_PATH_IMAGE113
and (3) representing the statistical standard deviation of the two-dimensional characteristic values of the single-layer two-dimensional lung electronic computer scanning image forming the three-dimensional image of the lung nodule.
The three-dimensional morphological feature vector in the three-dimensional feature vector of the lung nodule three-dimensional image is mainly obtained by extending two-dimensional morphological features, and specifically comprises the following steps: size, volume, area Difference, uniformity, integration, compact 3D, cube compact, project compact, distance to center of current Volume 3D, distance to center of project Volume, distance to Volume surface, juxtaplual 3D, fraction creating Volume 3D, organization X3D, organization Y3D, organization Z3D, X-Fraction 3D, Y-Fraction 3D, Z-Fraction 3D, X-Fraction 2D, Y-Fraction 2D, Z-Fraction 2D. The Size represents the maximum value of the distance between any two pixel points on the surface of the three-dimensional lung nodule, namely the diameter of an external sphere; volume represents the Volume of the three-dimensional lung nodule, and can be obtained by counting the number of three-dimensional pixels of the three-dimensional lung nodule and multiplying the number by the Volume of each three-dimensional pixel; the Area Difference represents the average variation of the areas of all the divided two-dimensional regions of a lung nodule, namely the sum of the variations between every two adjacent segments is divided by the number of the variations; the Sphericity of the three-dimensional pulmonary nodules is expressed by the Sphericity, the Sphericity is defined as taking a sphere with the same volume as the three-dimensional pulmonary nodules, the sphere center is taken through all pixel points in a pulmonary nodule body, meanwhile, the pixel number of the three-dimensional pulmonary nodules falling into the sphere is calculated, the maximum value of the number is taken to be multiplied by the volume of each pixel, and then the maximum value is divided by the volume of the sphere to be taken as the characteristic value of the Sphericity; elongation represents the eccentricity in three dimensions, defined as the ratio of the maximum diameter perpendicular to the maximum diameter of the three-dimensional pulmonary nodule to the maximum diameter; compact 3D represents sphere Compactness, defined as the volume of a three-dimensional lung nodule divided by the volume of a sphere of equal surface area; cube compact is defined as the ratio of the volume of a three-dimensional lung nodule to the volume of its bounding box in three-dimensional space; project compatibility is located as the ratio of the projected area of the three-dimensional lung nodule projected onto the x-y plane to the projected bounding box area; distance to center of current lung 3D is defined as the Euclidean Distance between the center of the three-dimensional lung nodule and the center of the whole lung. Wherein the center of the lung is the center of its bounding box; the center of the lung nodule is determined by a sphere which has the same volume with the lung nodule, the sphere and the lung nodule are superposed in a three-dimensional space, and when the superposed volume is the maximum, the position of the center of the sphere is the center of the lung nodule; distance to center of projected lung is defined as the Euclidean Distance between the center of the three-dimensional lung nodule and the center of the whole lung projected onto the x-y plane; distance to lung surface 3D is expressed as the minimum of the euclidean Distance between the center pixel of the three-dimensional lung nodule and the lung surface pixel; juxtapleural 3D represents whether the three-dimensional lung nodule region is in contact with a three-dimensional lung boundary, juxtapleura 3D is a Boolean feature, fraction touchhing 3D represents the contact degree of the three-dimensional lung nodule region and the three-dimensional lung boundary, and Fraction touchhing 3D is a Boolean feature; orientation X3D represents the included angle between the maximum diameter of a three-dimensional lung nodule in a three-dimensional space and the X axis; orientation Y3D represents the included angle between the maximum diameter of the three-dimensional pulmonary nodule in a three-dimensional space and the Y axis; orientation Z3D represents the included angle between the maximum diameter of the three-dimensional pulmonary nodule in a three-dimensional space and the Z axis; the X-Fraction 3D is defined as that the midpoint of the boundary in the X-axis direction of the boundary box of the half lung where the three-dimensional lung nodule is located is used as a reference point, and the distance between the center of the three-dimensional lung nodule and the reference point in the direction opposite to the X-axis direction is divided by the width of the boundary in the X-axis direction of the current boundary box; the Y-Fraction 3D is defined as taking the middle point of the boundary box of the half lung where the three-dimensional lung nodule is located in the Y-axis direction as a reference point, and dividing the distance between the center of the three-dimensional lung nodule and the reference point in the relative Y-axis direction by the width of the boundary box in the Y-axis direction at present; the Z-Fraction 3D is defined as taking the middle point of the boundary box of the half lung where the three-dimensional lung nodule is located in the Z-axis direction as a reference point, and dividing the distance between the center of the three-dimensional lung nodule and the reference point in the relative Z-axis direction by the width of the boundary box in the Z-axis direction; the X-Fraction 2D is defined as that the midpoint of the boundary in the X-axis direction of the whole lung boundary box is taken as a reference point, and the distance between the center of the three-dimensional lung nodule and the reference point in the relative X-axis direction is divided by the boundary width in the X-axis direction of the current boundary box; the Y-Fraction 2D is defined as that the midpoint of the boundary in the Y-axis direction of the boundary box of the whole lung is taken as a reference point, and the distance between the center of the three-dimensional lung nodule and the reference point in the relative Y-axis direction is divided by the boundary width in the Y-axis direction of the current boundary box; the Z-Fraction 2D is defined as taking the middle point of the boundary box of the whole lung in the Z-axis direction as a reference point, and dividing the distance between the center of the three-dimensional lung nodule and the reference point in the Z-axis direction by the width of the boundary box in the Z-axis direction.
The three-dimensional gray level feature vector in the three-dimensional feature vector is a three-dimensional mapThe statistics of the gray level in the image are specifically divided into the following three aspects: statistical aspects (features of the statistical aspects include Maximum, minimum, mean, std, standard deviation, skew, kurtosis, etc.)), regional aspects (features of the regional aspects include, inner, outer 1, outer 2, outer 3, outer Z, above, and below), and comparative aspects (features of the comparative aspects include, separation1, separation2, separation3, separation Z, constrast 11, constrast 12, constrast 13, constrast 1Z, constrast 21, constrast 22, constrast 23, and constrast 2Z). Each specific three-dimensional gray level feature vector is formed by combining features in a statistical aspect and features in a region aspect or features in a contrast aspect, for example: and a three-dimensional gray feature vector such as Maximum _ inside and Maximum _ section 1. Regional characteristics are based on the division of different regions, in this embodiment, inside represents the internal region of the three-dimensional lung nodule, please refer to fig. 3, and the original three-dimensional lung nodule is obtained through the dilation operation in mathematical morphology by different 4 structural elements: the structural element a is a spheroid structural element, and in an x-y plane corresponding to a three-dimensional pulmonary nodule, by taking a pixel layer of a circle with the radius of 5 pixel points as a center, the same pixel layer is respectively expanded up and down in the z-axis direction to obtain an outside1 region of the spheroid structural element, as shown in fig. 3 (a); the structural element b is also a spheroid structural element, and in an x-y plane corresponding to the three-dimensional pulmonary nodule, by taking a pixel layer of a circle with a radius of 10 pixel points as a center, the same pixel layer is respectively expanded up and down in the z-axis direction to obtain outside2 regions of the spheroid structural element, as shown in fig. 3 (b); the structural element c is a circular structural element, that is, a circular pixel layer with radius of x-y plane corresponding to the three-dimensional pulmonary nodule being 10 pixel points obtains outside3 region of the circular structural element, as shown in fig. 3 (c); the structural element d is a columnar structural element, one pixel of the x-y plane corresponding to the three-dimensional lung nodule serves as a pixel layer, and then such a layer of pixels is expanded up and down in the z-axis direction to obtain an outsolid z region, as shown in fig. 3 (d). Above indicates the maximum value of the three-dimensional pulmonary nodule in the Z axisThe area obtained by projecting the upper layer of one pixel point on the x-y plane. Below represents the area obtained by the projection of the next layer of the three-dimensional pulmonary nodule on the x-y plane at the pixel point with the minimum Z-axis value. The features for the comparison aspect, namely, segmentation 1, segmentation 2, segmentation 3, segmentation Z, concentrate 11, concentrate 12, concentrate 13, concentrate 1Z, concentrate 21, concentrate 22, concentrate 23 and concentrate 2Z, can be classified into three categories: seperationi, concentrate 1I, and concentrate 2I. Wherein, section I represents the difference between a certain characteristic of an inside region and the same characteristic vector in outsid I (I =1,2,3, Z), and the section I specifically satisfies the following formula:
Figure 424761DEST_PATH_IMAGE114
(ii) a The contist 1I represents a class of characteristic value of the region minus the corresponding class of characteristic value of the outseI (I =1,2,3, Z) in the inside region, and the contist 1I specifically satisfies the following formula
Figure 54326DEST_PATH_IMAGE115
(ii) a Conttrast 2I represents the ratio of conttrast 1I divided by the sum of the standard deviations of the features in the inside and outeideI regions, and is specifically defined as
Figure 149321DEST_PATH_IMAGE116
And are and
Figure 802019DEST_PATH_IMAGE117
indicate the standard deviation corresponding to the same class of features in the inner and outer idei regions, respectively.
The three-dimensional gradient features include: three-dimensional gradient feature vector
Figure 499717DEST_PATH_IMAGE119
Component features in X, Y, Z axes
Figure 124733DEST_PATH_IMAGE120
Figure 249684DEST_PATH_IMAGE121
Figure 327361DEST_PATH_IMAGE122
Three-dimensional gradient feature vector
Figure 94329DEST_PATH_IMAGE119
Contrast feature vector and three-dimensional gradient feature vector on X and Y axes
Figure 573852DEST_PATH_IMAGE119
Contrast feature vector and three-dimensional gradient feature vector on X and Z axes
Figure 807387DEST_PATH_IMAGE119
Contrast feature vector and three-dimensional gradient feature vector on Z axis and Y axis
Figure 502854DEST_PATH_IMAGE119
Gradient magnitude feature (gradient magnitude) of (1), three-dimensional gradient feature vector
Figure 417720DEST_PATH_IMAGE119
Radial-deviation characterization, three-dimensional gradient eigenvectors
Figure 876383DEST_PATH_IMAGE119
Radial-gradient feature (radial-gradient). The method comprises the steps of obtaining a lung nodule expansion operation, wherein the lung nodule expansion operation comprises a gradient amplitude characteristic (gradient magnitude), a radial deviation characteristic (radial-deviation) and a radial gradient characteristic (radial-gradient), and further comprises the steps of classifying the interior (inside) of a two-dimensional region of the lung nodule, the inner boundary (perimeter inside) of the two-dimensional region of the lung nodule, an extra region (outeidel, I =1,2,3, Z) obtained after the lung nodule expansion operation by morphology, and the outer boundary (perimeter outeidel) of the extra region according to positions, wherein a specific classification mode and a specific calculation mode can be obtained by analogy through two-dimensional plane gradient characteristic operation. Three-dimensional gradient feature vector
Figure 484082DEST_PATH_IMAGE119
The three-dimensional vector can be decomposed into three-dimensional analysis in X, Y and Z directions (in the specification, the X, Y and Z directions are three-dimensional analysis formed based on single-layer lung electron computer tomography image definitionImage defined), i.e. three-dimensional gradient feature vectors
Figure 333089DEST_PATH_IMAGE119
Can be expressed as
Figure 176280DEST_PATH_IMAGE123
For the gradient of any pixel point to be analyzed, as shown in fig. 4, a square field pixel can be confirmed first, 9 pixels on the upper layer are numbered 1 to 9 sequentially from top to bottom in the square field pixel from a center point pixel to the left, and 9 pixels on the lower layer are numbered 10 to 18 sequentially in the same order, wherein the components of the three-dimensional feature vector are numbered
Figure 630396DEST_PATH_IMAGE124
The components satisfy the following formula:
Figure 268050DEST_PATH_IMAGE125
wherein, the first and the second end of the pipe are connected with each other,
Figure 807616DEST_PATH_IMAGE126
representing the gray value of the pixel point with the number i in the square field pixel,
Figure 454498DEST_PATH_IMAGE127
the weight of the pixel point numbered i is represented,
Figure 559857DEST_PATH_IMAGE128
which is
Figure 509359DEST_PATH_IMAGE129
In the step (1), the first step,
Figure 129696DEST_PATH_IMAGE130
representing the coordinates of a central pixel point
Figure 455635DEST_PATH_IMAGE131
To the pixel point coordinate with number i
Figure 743397DEST_PATH_IMAGE132
The euclidean distance between them. Component of three-dimensional feature vector for center point pixel
Figure 660537DEST_PATH_IMAGE133
And component(s)
Figure 174695DEST_PATH_IMAGE134
Can be obtained in the same manner. Three dimensional gradient feature
Figure 897801DEST_PATH_IMAGE135
Is defined as a characteristic magnitude of
Figure 915435DEST_PATH_IMAGE136
(ii) a Radial-deviation (radial-deviation) is expressed as the included angle between the gradient vector on any central pixel point and the radial direction (the radial direction represents the connecting line of the central pixel point and the center point of the pulmonary nodule and points to the central direction of the pulmonary nodule)
Figure 596952DEST_PATH_IMAGE137
(ii) a Radial-gradient (radial-gradient) is expressed as the projection size of the gradient vector of any central pixel point in the radial direction and is defined as
Figure 332827DEST_PATH_IMAGE138
In the step S02, a plurality of characteristic vectors for representing the characteristics of the lung nodules are set according to the two-dimensional and three-dimensional characteristics of the lung nodules in the lung electron computed tomography image, so that comprehensive and accurate theory and data support are provided for subsequent extraction and judgment of the lung nodules to be judged, and the accuracy of judgment results is improved.
S03, extracting a first pulmonary nodule feature vector in a pulmonary electronic computed tomography image of the known good and malignant condition of the pulmonary nodule.
The extracting of the first lung nodule feature vector in the lung CT image of the known good and malignant lung nodule in step S03 may be performed by writing a corresponding program to perform corresponding extraction on the feature vector in the lung CT image of the known good and malignant lung nodule according to the basic definition of the feature vector in step S02. And then, calculating the characteristic value through the extracted characteristic vector, thereby obtaining all information of the first lung nodule characteristic vector, namely the first lung nodule characteristic vector with the corresponding characteristic value.
And S04, obtaining various clustering results through the first lung nodule characteristic vector, and generating a reference clustering data set through the various clustering results.
In step S04, obtaining a plurality of clustering results through the first lung nodule feature vector, and generating a reference clustering data set through the plurality of clustering results, including the following steps: carrying out clustering analysis on the first lung nodule characteristic vector by utilizing different clustering algorithms to obtain a plurality of clustering results, or carrying out clustering analysis on the first lung nodule characteristic vector by utilizing the same clustering algorithm with different parameters and different initial values to obtain a plurality of clustering results; and combining the multiple clustering results to obtain a combined result, and carrying out clustering analysis on the combined result to obtain a reference clustering data set.
Hierarchical clustering is a static clustering algorithm, which is divided into a merging algorithm and a splitting algorithm. The merging algorithm reduces the number of cluster centers at each step, and the clustering results from the merging of the two clusters from the previous step. The splitting algorithm is opposite to the merging algorithm in principle, the number of the clustering centers is increased in each step, and the result generated by clustering in each step is obtained by splitting one clustering center in the previous step into two clustering centers. The Kmeans clustering method is a dynamic clustering algorithm, and can minimize the sum of squares of distances from all samples in a clustering domain to a clustering center. The clustering method for obtaining multiple clustering results in step S04 includes, but is not limited to: and clustering algorithms such as a Kmeans clustering method, an HC clustering algorithm, a MeanShift algorithm, a Kmeans & HC combined clustering algorithm and the like. According to the method, the first lung nodule characteristic vector is subjected to multiple clustering analysis through a dynamic clustering algorithm and a static clustering algorithm, and multiple clustering results obtained are strong in robustness. The combination of the multiple clustering results to obtain the combined result includes but is not limited to a Kmeans clustering method, an HC clustering algorithm, a MeanShift algorithm, a Kmeans & HC combined clustering algorithm and other clustering algorithms.
In an alternative embodiment, a Kmeans clustering method is adopted, and a clustering combination of multiple clustering results is obtained by performing clustering analysis on the first lung nodule feature vector by using different k values and initial clustering centers: p = { P 1 ,P 2 ,…, P N Within a certain range of k min ,k max ]Inner variation, each time clustering selects a different initial cluster center. Each P l Obtaining an autocorrelation matrix C l Autocorrelation matrix C l The following formula is satisfied:
Figure 531727DEST_PATH_IMAGE139
combining a plurality of clustering results in the clustering combination through a voting mechanism to obtain a combined result as follows:
Figure 794081DEST_PATH_IMAGE140
wherein the content of the first and second substances,
Figure 256287DEST_PATH_IMAGE141
a matrix obtained by combining a plurality of kinds of clustering results is represented,
Figure 338512DEST_PATH_IMAGE142
Figure 606683DEST_PATH_IMAGE143
representation matrix
Figure 598909DEST_PATH_IMAGE141
Middle sample
Figure 91071DEST_PATH_IMAGE144
And samples
Figure 801538DEST_PATH_IMAGE146
The corresponding value at the indicated position is,
Figure 935716DEST_PATH_IMAGE147
representing the total number of clustering results. Then the combined result is hierarchically clustered, and a single connection method SL is selected to connect the matrix
Figure 579187DEST_PATH_IMAGE148
As a sample distance matrix for the SL algorithm. Defining a threshold value to determine the final clustering result of SL, wherein the threshold value is the lifetime of k-cluster division and is marked as l k The lifetime is the difference in ordinate from the level at which the k classes are generated to the level at which the k-1 clusters are generated. And finally, taking the layer with the largest lifetime as a final clustering layer, and obtaining a final clustering result which is the reference clustering data set. The feature vectors in the reference cluster dataset have already calibrated the benign and malignant properties of the corresponding lung nodule.
S05, extracting a second pulmonary nodule feature vector in the lung electronic computed tomography image of the benign and malignant condition of the pulmonary nodule to be detected.
The method for extracting the second lung nodule feature vector in the lung electronic computed tomography image of the benign and malignant condition of the lung nodule in the step S05 can be similar to the method for extracting the first lung nodule feature vector in the step S03.
And S06, detecting benign lung nodules and malignant lung nodules in the lung electron computed tomography image of the benign and malignant condition of the lung nodules to be detected by using the second lung nodule feature vector and combining the reference clustering data set.
Step S06, detecting benign lung nodules and malignant lung nodules in the lung electron computed tomography image of the benign and malignant condition of the lung nodules to be detected by using the second lung nodule feature vector in combination with the reference cluster data set, including the following steps:
s601, obtaining lung nodule feature vector x aiming at ith malignancy feature subclass in reference clustering data set respectively
Figure 648774DEST_PATH_IMAGE149
Bayes posterior probability of (2)
Figure 440012DEST_PATH_IMAGE150
And the jth benign feature subclass
Figure 253247DEST_PATH_IMAGE151
Bayes posterior probability of
Figure 344700DEST_PATH_IMAGE152
. Bayes posterior probability
Figure 319610DEST_PATH_IMAGE153
And
Figure 801406DEST_PATH_IMAGE154
respectively satisfy the following formulas:
Figure 277387DEST_PATH_IMAGE155
Figure 833133DEST_PATH_IMAGE156
wherein, in the step (A),
Figure 97718DEST_PATH_IMAGE157
representing a malignancy feature subclass
Figure 4494DEST_PATH_IMAGE158
The average of the feature vectors of the respective samples,
Figure 284166DEST_PATH_IMAGE159
representing a malignant feature subclass
Figure 756736DEST_PATH_IMAGE160
The covariance matrix of the eigenvectors of each sample,
Figure 339027DEST_PATH_IMAGE161
indicating to subclass malignancy characteristics
Figure 592154DEST_PATH_IMAGE160
Distribution of
Figure 285303DEST_PATH_IMAGE162
The number of times of the total number of the components,
Figure 205855DEST_PATH_IMAGE163
representing a malignant feature subclass
Figure 755785DEST_PATH_IMAGE164
The average of the feature vectors of the respective samples,
Figure 371574DEST_PATH_IMAGE165
representing a malignancy feature subclass
Figure 727469DEST_PATH_IMAGE164
The covariance matrix of the eigenvectors of each sample,
Figure 377893DEST_PATH_IMAGE166
representing benign feature subclasses
Figure 426620DEST_PATH_IMAGE167
The average of the feature vectors of the respective samples,
Figure 795285DEST_PATH_IMAGE168
benign feature subclass
Figure 626975DEST_PATH_IMAGE167
The covariance matrix of the eigenvectors of each sample.
S602, setting a quality determination boundary
Figure 256539DEST_PATH_IMAGE169
The benign-malignant determination boundary satisfies the following equation:
Figure 85955DEST_PATH_IMAGE170
and S603, converting the boundary formula into a Markov space linear decision equation through a good and malignant decision boundary formula. And (3) solving the natural logarithm of two sides of the good and malignant judgment boundary formula, and obtaining the following formula after deformation:
Figure 800970DEST_PATH_IMAGE171
order to
Figure 436351DEST_PATH_IMAGE172
It can be further simplified to the following formula:
Figure 61367DEST_PATH_IMAGE173
wherein, in the process,
Figure 451897DEST_PATH_IMAGE175
and with
Figure 529574DEST_PATH_IMAGE176
Is a constant value that can be adjusted,
Figure 765384DEST_PATH_IMAGE177
for the feature vector x to the jth benign feature subclass
Figure 244907DEST_PATH_IMAGE178
The Mahalanobis distance of the center can be made to be
Figure 478442DEST_PATH_IMAGE179
Figure 168049DEST_PATH_IMAGE180
Is the feature vector x to the ith malignancy feature subclass
Figure 348495DEST_PATH_IMAGE181
The Mahalanobis distance of the center can be made to be
Figure 807158DEST_PATH_IMAGE182
Therefore, the mahalanobis space linear decision equation satisfies the following formula:
Figure 414857DEST_PATH_IMAGE183
wherein, the first and the second end of the pipe are connected with each other,
Figure 998285DEST_PATH_IMAGE184
representing feature vectors x through jth benign feature subclass
Figure 107055DEST_PATH_IMAGE185
The mahalanobis distance of the center of the circle,
Figure 561170DEST_PATH_IMAGE186
representing feature vectors x through the ith malignancy feature subclass
Figure 198825DEST_PATH_IMAGE187
The mahalanobis distance of the center of the circle,
Figure 472812DEST_PATH_IMAGE188
is the ith malignancy feature subclass
Figure 119694DEST_PATH_IMAGE189
The expansion times are increased by a plurality of times,
Figure 225053DEST_PATH_IMAGE190
is a linear intercept parameter.
S604, obtaining the Bayes posterior probability of the second pulmonary nodule feature vector
Figure DEST_PATH_IMAGE191
Value of (d) and Bayesian posterior probability
Figure 768030DEST_PATH_IMAGE192
The value of (c).
S605, preliminarily judging the benign and malignant degree of the second pulmonary nodule characteristic vector according to a benign and malignant degree judgment boundary formula, wherein the benign and malignant degree judgment satisfies the following formula:
Figure DEST_PATH_IMAGE193
s606, respectively calculating the second lung nodule feature vector to the jth benign feature subclass
Figure 128647DEST_PATH_IMAGE185
Mahalanobis distance of center
Figure 985744DEST_PATH_IMAGE194
And to the ith malignancy feature subclass
Figure DEST_PATH_IMAGE195
Mahalanobis distance of center
Figure DEST_PATH_IMAGE197
S607, according to the Mahalanobis distance
Figure 211189DEST_PATH_IMAGE194
And said Mahalanobis distance
Figure 456226DEST_PATH_IMAGE197
Combined decision coordinates
Figure 501542DEST_PATH_IMAGE198
At the mahalanobis location, the second lung nodule feature vector is again determined to be benign or malignant:
if the second lung nodule feature vector belongs to the benign feature after the primary judgment, the judgment coordinate corresponding to the second lung nodule feature vector
Figure 365593DEST_PATH_IMAGE198
If the second lung nodule characteristic vector is positioned below the Mahalanobis space linear judgment straight line, the second lung nodule characteristic vector is false positive; if the second lung nodule feature vector is judged to belong to the malignant feature for the first time, judging coordinates corresponding to the second lung nodule feature vector
Figure DEST_PATH_IMAGE199
And if the second lung nodule feature vector is positioned above the linear judgment straight line in the Mahalanobis space, the second lung nodule feature vector is false negative.
And S608, optimizing the Mahalanobis space linear decision equation parameters to detect all benign lung nodules when the number of the second lung nodule feature vectors which are false positive is minimum. See FIG. 5 for a view in Mahalanobis spaceIn the linear judgment space, the abscissa is the mahalanobis distance of the distribution center of a certain subclass of the second pulmonary nodule feature vector and the malignant classification in the feature space, the ordinate is the mahalanobis distance equation of the distribution center of a certain subclass of the second pulmonary nodule feature vector and the benign classification in the feature space, and when the parameters in the mahalanobis space linear judgment equation are adjusted
Figure 976703DEST_PATH_IMAGE200
When the value is taken, the change of the straight line in the mahalanobis space linearity determination space is as shown in fig. 5 (a); when adjusting parameters in the mahalanobis space linear decision equation
Figure DEST_PATH_IMAGE201
When the values are taken, the change of the straight line in the mahalanobis space linearity determination space is as shown in fig. 5 (b). By varying parameters
Figure 658220DEST_PATH_IMAGE200
And
Figure 394095DEST_PATH_IMAGE201
and an optimal linear discriminant function can be obtained, so that all negative lung nodules can be detected when the number of false-positive second lung nodule feature vectors is minimum, and the accuracy of judgment is greatly guaranteed.
The invention extracts a plurality of characteristic vectors of lung electron computer tomography images of known benign and malignant conditions of lung nodules, generates a reference cluster data set for judging the benign and malignant conditions of the lung nodules after cluster analysis, and identifies the extracted second lung nodule characteristic vectors and diagnoses the benign and malignant conditions of the lung nodules to be judged by using the reference cluster data set. According to the method, a stable and reliable lung nodule reference clustering data set is generated through clustering analysis of a large number of lung nodule benign and malignant data judged by medical clinical certification and doctor experience, efficient and rapid identification and diagnosis of the lung nodule to be judged are realized through the reference clustering data set, and doctors are effectively assisted in diagnosing and treating benign and malignant pathologies of the lung nodule.
Referring to fig. 6, the present invention also provides an apparatus for detecting benign and malignant pulmonary nodules comprising one or more processors 601; one or more input devices 602, one or more output devices 603, and memory 604. The processor 601, the input device 602, the output device 603, and the memory 604 are connected by a bus 605. The memory 604 may be the computer readable storage medium of any one of the aspects provided herein, and the processor 601 is configured to invoke the program instructions contained in the computer storage medium provided herein for detecting benign and malignant lung nodules.
In an alternative embodiment, processor 601 may be a Central Processing Unit (CPU), which may be other general purpose Processor, a Digital Signal Processor (DSP), an Application Specific Integrated Circuit (ASIC), an FPGA (Field-Programmable Gate Array) or other Programmable logic device, discrete Gate or transistor logic, discrete hardware components, or the like. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like. The input device 602 may be used to acquire an electron computed tomography image of the lung of a known good-malignancy condition of a lung nodule and a condition of a lung nodule to be detected. The output device 603 may be configured to output the benign and malignant condition of the lung nodule to be detected, which is obtained through program instructions stored in any one of the computer-readable storage media provided in the present invention, to a target terminal for displaying. The memory 604 may include both read-only memory and random access memory, and provides instructions and data to the processor 601. A portion of the memory 604 may also include non-volatile random access memory. For example, the memory 604 may also store device type information.
In yet another alternative embodiment, the processor 601, the input device 602, and the output device 603 described in this embodiment of the present invention may execute an implementation manner described in a program instruction stored in any computer-readable storage medium provided by the present invention, and may also execute an implementation manner of a terminal device described in this embodiment of the present invention, which is not described herein again. The computer-readable storage medium may be an internal storage unit of the terminal device in any of the foregoing embodiments, for example, a hard disk or a memory of the terminal device. The computer-readable storage medium may also be an external storage device of the terminal device, such as a plug-in hard disk, a Smart Media Card (SMC), a Secure Digital (SD) Card, a Flash memory Card (Flash Card), and the like provided on the terminal device. Further, the computer-readable storage medium may include both an internal storage unit and an external storage device of the terminal device. The computer-readable storage medium is used for storing the computer program and other programs and data required by the terminal device. The above-described computer-readable storage medium may also be used to temporarily store data that has been output or is to be output.
Finally, it should be noted that: the above embodiments are only used to illustrate the technical solution of the present invention, and not to limit the same; while the invention has been described in detail and with reference to the foregoing embodiments, it will be understood by those skilled in the art that: the technical solutions described in the foregoing embodiments may still be modified, or some or all of the technical features may be equivalently replaced; such modifications and substitutions do not depart from the spirit and scope of the present invention, and they should be construed as being included in the following claims and description.

Claims (10)

1. A computer storage medium for detecting pulmonary nodule malignancy and well, the computer storage medium storing a computer program comprising program instructions that, when executed by a processor, cause the processor to perform the steps of:
acquiring lung electron computer tomography images of known good and malignant conditions of lung nodules and good and malignant conditions of lung nodules to be detected;
setting a lung nodule characteristic vector in a lung electron computed tomography image;
extracting a first pulmonary nodule feature vector in a pulmonary electron computed tomography image of a known benign and malignant condition of a pulmonary nodule;
obtaining a plurality of clustering results through the first lung nodule feature vector, and generating a reference clustering data set through the plurality of clustering results;
extracting a second pulmonary nodule characteristic vector in the lung electronic computed tomography image of the benign and malignant condition of the pulmonary nodule to be detected;
and detecting benign lung nodules and malignant lung nodules in the lung electron computed tomography image of the benign and malignant condition of the lung nodules to be detected by utilizing the second lung nodule feature vector and combining the reference cluster data set.
2. The computer storage medium for detecting benign and malignant lung nodules according to claim 1, wherein said setting lung nodule feature vectors in lung electron computed tomography images comprises the steps of:
setting two-dimensional feature vectors in a single-layer lung electron computed tomography image, wherein the two-dimensional feature vectors comprise two-dimensional morphological feature vectors, two-dimensional gray-scale feature vectors and two-dimensional gradient feature vectors;
and superposing a plurality of single-layer lung electron computed tomography images to form a lung nodule three-dimensional image, and setting a three-dimensional characteristic vector of the lung nodule three-dimensional image, wherein the three-dimensional characteristic vector comprises a three-dimensional morphological characteristic vector, a three-dimensional gray characteristic vector and a three-dimensional ladder characteristic vector.
3. The computer storage medium for detecting benign and malignant lung nodules according to claim 2, wherein said three-dimensional grayscale feature vector comprises a contrast-wise grayscale feature vector comprising:
Figure 728325DEST_PATH_IMAGE001
Figure 459521DEST_PATH_IMAGE002
Figure 718464DEST_PATH_IMAGE003
wherein, inside represents the inner region of the three-dimensional lung nodule,
Figure 941635DEST_PATH_IMAGE004
Figure 537701DEST_PATH_IMAGE005
representing the expanded peripheral region of the three-dimensional lung nodule,
Figure 264349DEST_PATH_IMAGE006
and
Figure 22089DEST_PATH_IMAGE007
are shown in imide and
Figure 529294DEST_PATH_IMAGE005
the same class of features within a region may,
Figure 538838DEST_PATH_IMAGE008
and
Figure 510205DEST_PATH_IMAGE009
are shown in imide and
Figure 314213DEST_PATH_IMAGE005
and standard deviations corresponding to the same type of features in the region respectively.
4. The computer storage medium for detecting benign and malignant lung nodules according to claim 2, wherein said three-dimensional gradient feature vectors comprise components of gradient feature vectors on three-dimensional coordinate axes
Figure 371031DEST_PATH_IMAGE011
Component (a) of
Figure 184266DEST_PATH_IMAGE011
The following formula is satisfied:
Figure 682244DEST_PATH_IMAGE012
wherein the content of the first and second substances,
Figure 47366DEST_PATH_IMAGE013
Figure 466846DEST_PATH_IMAGE014
representing the components of the three-dimensional gradient feature vector on the X-axis,
Figure 677248DEST_PATH_IMAGE015
representing the components of the three-dimensional gradient feature vector in the Y-axis,
Figure 498573DEST_PATH_IMAGE016
representing the component of the three-dimensional gradient feature vector in the Z-axis,
Figure 34597DEST_PATH_IMAGE017
the gray value of a pixel point which is numbered as i in pixels in the square field of a central pixel point of the three-dimensional ladder characteristic vector is represented,
Figure 738110DEST_PATH_IMAGE018
representing the weight of the pixel point numbered i,
Figure 893148DEST_PATH_IMAGE019
in which
Figure 428035DEST_PATH_IMAGE020
Figure 10326DEST_PATH_IMAGE021
Figure 534891DEST_PATH_IMAGE022
Representing the coordinates of a central pixel
Figure 228041DEST_PATH_IMAGE023
To the pixel point coordinate with number i
Figure 820696DEST_PATH_IMAGE024
The euclidean distance between them.
5. The computer storage medium for detecting benign and malignant lung nodules according to claim 1, wherein said obtaining a plurality of kinds of clustering results through said first lung nodule feature vector, and generating a reference clustering dataset through said plurality of kinds of clustering results, comprises the steps of:
carrying out clustering analysis on the first lung nodule characteristic vector by utilizing different clustering algorithms to obtain a plurality of clustering results; or alternatively
Performing clustering analysis on the first pulmonary nodule characteristic vector through the same clustering algorithm with different parameters and different initial values to obtain a plurality of clustering results;
and combining the multiple clustering results to obtain a combined result, and performing clustering analysis on the combined result to obtain a reference clustering data set.
6. The computer storage medium for detecting benign and malignant pulmonary nodules according to claim 5, wherein said different clustering algorithms comprise a Kmeans clustering method, a HC clustering algorithm, a MeanShift algorithm, and a Kmeans-HC combination clustering algorithm.
7. The computer storage medium for detecting benign and malignant lung nodules according to claim 5, wherein said combined result satisfies the following formula:
Figure 432943DEST_PATH_IMAGE025
wherein, the first and the second end of the pipe are connected with each other,
Figure 48732DEST_PATH_IMAGE026
a matrix obtained by combining a plurality of kinds of clustering results is represented,
Figure 670206DEST_PATH_IMAGE027
Figure 320630DEST_PATH_IMAGE028
representation matrix
Figure 369358DEST_PATH_IMAGE029
Middle sample
Figure 269181DEST_PATH_IMAGE030
And samples
Figure 304133DEST_PATH_IMAGE031
The corresponding value at the indicated position is,
Figure 933697DEST_PATH_IMAGE032
Figure 28692DEST_PATH_IMAGE033
representing the total number of clustering results.
8. The computer storage medium for detecting benign and malignant lung nodules according to claim 1, wherein said detecting benign and malignant lung nodules in the lung EMCT images of the condition of benign and malignant lung nodules to be detected using said second lung nodule feature vector in combination with said reference cluster data set comprises the steps of:
obtaining pulmonary nodule feature vectors
Figure 743707DEST_PATH_IMAGE034
Pin for sortingFor the ith malignancy feature subclass in the reference cluster dataset
Figure 582350DEST_PATH_IMAGE035
Bayes posterior probability of (2)
Figure 4105DEST_PATH_IMAGE036
And the jth benign feature subclass
Figure 394635DEST_PATH_IMAGE037
Bayes posterior probability of
Figure 206733DEST_PATH_IMAGE038
Setting a quality/malignancy determination boundary
Figure 708121DEST_PATH_IMAGE039
The benign-malignant determination boundary satisfies the following formula:
Figure 187644DEST_PATH_IMAGE040
converting the good and malignant judgment boundary formula into a Markov space linear judgment equation;
obtaining a Bayesian posterior probability of the second pulmonary nodule feature vector
Figure 421179DEST_PATH_IMAGE036
And Bayes posterior probability
Figure 110787DEST_PATH_IMAGE038
And preliminarily judging the benign and malignant degree of the second lung nodule characteristic vector according to a benign and malignant degree judgment boundary formula, wherein the benign and malignant degree judgment satisfies the following formula:
Figure 25653DEST_PATH_IMAGE041
respectively calculating the second lung nodule feature vector to the jth benign feature subclass
Figure 484316DEST_PATH_IMAGE042
Mahalanobis distance of center
Figure 92015DEST_PATH_IMAGE043
And to the ith malignancy feature subclass
Figure 941022DEST_PATH_IMAGE044
Mahalanobis distance of center
Figure 49793DEST_PATH_IMAGE045
According to the Mahalanobis distance
Figure 972749DEST_PATH_IMAGE046
And said Mahalanobis distance
Figure 875983DEST_PATH_IMAGE047
Combined decision coordinates
Figure 415549DEST_PATH_IMAGE048
At the mahalanobis location, the second lung nodule feature vector is again determined to be benign or malignant: if the second lung nodule feature vector belongs to the benign feature after the primary judgment, the judgment coordinate corresponding to the second lung nodule feature vector
Figure 734535DEST_PATH_IMAGE049
If the second lung nodule feature vector is located below the mahalanobis space linear judgment straight line, the second lung nodule feature vector is false positive; if the second lung nodule feature vector is judged to belong to the malignant feature for the first time, judging coordinates corresponding to the second lung nodule feature vector
Figure 167790DEST_PATH_IMAGE049
Is located above the linear judgment straight line of the Mahalanobis space, thenThe second lung nodule feature vector is false negative;
all benign lung nodules are detected by optimizing the mahalanobis space linear decision equation parameters such that the number of false positive second lung nodule feature vectors is minimized.
9. The computer storage medium for detecting benign and malignant lung nodules according to claim 8, wherein said mahalanobis space linear decision equation satisfies the following formula:
Figure 851713DEST_PATH_IMAGE050
wherein the content of the first and second substances,
Figure 3208DEST_PATH_IMAGE051
representing feature vectors x through the jth benign feature subclass
Figure 63568DEST_PATH_IMAGE052
The mahalanobis distance of the center of the circle,
Figure 23434DEST_PATH_IMAGE053
representing feature vectors x through the ith malignancy feature subclass
Figure 534050DEST_PATH_IMAGE054
The mahalanobis distance of the center of the circle,
Figure 782628DEST_PATH_IMAGE055
is the first malignancy feature subclass
Figure 505734DEST_PATH_IMAGE054
The expansion times are increased by a plurality of times,
Figure 788948DEST_PATH_IMAGE056
is a linear intercept parameter.
10. An apparatus for detecting the malignancy and/or malignancy of a lung nodule, comprising a processor, an input device, an output device, and a memory interconnected with one another, the memory including a computer storage medium according to any one of claims 1 to 9, the processor being configured to invoke the program instructions.
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