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CN101853376A - A computer-aided detection method for breast microcalcifications - Google Patents

A computer-aided detection method for breast microcalcifications Download PDF

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CN101853376A
CN101853376A CN201010111555A CN201010111555A CN101853376A CN 101853376 A CN101853376 A CN 101853376A CN 201010111555 A CN201010111555 A CN 201010111555A CN 201010111555 A CN201010111555 A CN 201010111555A CN 101853376 A CN101853376 A CN 101853376A
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CN101853376B (en
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张二虎
王帆
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Xian University of Technology
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Abstract

本发明公开了一种乳腺微钙化点计算机辅助检测方法,先对乳腺图像进行灰度校正变换,得到灰度校正后图像;然后采用基于双结构元素的背景叠加法,得到微钙化点增强的乳腺图像,同时采用形态学中的Top-hat变换方法,得到另一幅背景抑制的乳腺图像;再对这两幅图像采用双阈值进行分割得到初步的微钙化点图像,经过后处理形成微钙化点粗检图像;对粗检出的微钙化点目标区域,提取特征,用支持向量机的进行分类,去掉假的微钙化点目标区域,将剩下的标记到乳腺图像中去,供医生阅片用。采用本发明方法,可以将医生从繁琐的阅片、分类工作中解脱出来,辅助医生对图像进行更好的理解和判断,从而降低误诊与漏诊,达到提高诊断正确率的目的。

Figure 201010111555

The invention discloses a computer-aided detection method for mammary gland microcalcification points. Firstly, the mammary gland image is grayscale corrected and transformed to obtain the grayscale corrected image; At the same time, the Top-hat transformation method in morphology is used to obtain another background-suppressed breast image; the two images are then segmented by double threshold to obtain a preliminary image of micro-calcification points, which are post-processed to form micro-calcification points Roughly inspect the image; extract features from the roughly detected microcalcification target area, use support vector machine to classify, remove the false microcalcification target area, and mark the rest into the breast image for doctors to read use. By adopting the method of the invention, the doctor can be freed from the tedious work of image reading and classification, and assist the doctor to better understand and judge the images, thereby reducing misdiagnosis and missed diagnosis, and achieving the purpose of improving the correct rate of diagnosis.

Figure 201010111555

Description

一种乳腺微钙化点计算机辅助检测方法 A computer-aided detection method for breast microcalcifications

技术领域technical field

本发明属于医学影像自动分析处理技术领域,具体涉及一种乳腺微钙化点计算机辅助检测方法。The invention belongs to the technical field of automatic analysis and processing of medical images, and in particular relates to a computer-aided detection method for breast microcalcification points.

背景技术Background technique

乳腺癌是世界各地女性最常见的恶性肿瘤之一,严重威胁着女性的健康甚至生命。在北欧、西方等发达国家,乳腺癌发病率居女性恶性肿瘤发病率首位。在我国,随着人们生活饮食习惯的改变,乳腺癌的发病率也呈现明显的上升趋势,其中25-34岁的女性乳腺癌发病率也增长很快。近几十年,随着医学技术的发展,乳腺癌的诊断和治疗技术有了较大的进步,尽管如此,乳腺癌的死亡率并没有明显下降,这主要是由于多数乳腺癌被发现时已经较晚,难以治愈。因此,在乳腺癌病因预防尚不确定的情况下,及早发现是降低患者死亡率的关键。Breast cancer is one of the most common malignant tumors in women all over the world, which seriously threatens women's health and even life. In developed countries such as Northern Europe and the West, the incidence of breast cancer ranks first in the incidence of female malignant tumors. In my country, with the change of people's living and eating habits, the incidence of breast cancer has also shown an obvious upward trend, and the incidence of breast cancer among women aged 25-34 has also increased rapidly. In recent decades, with the development of medical technology, the diagnosis and treatment of breast cancer have made great progress. However, the mortality rate of breast cancer has not decreased significantly, which is mainly due to the fact that most breast cancers have already been diagnosed when they are discovered. Later, difficult to cure. Therefore, when the etiology and prevention of breast cancer are still uncertain, early detection is the key to reducing the mortality of patients.

目前,乳腺癌诊断采用的主要方法是钼靶软X射线检查,其中微钙化点和肿块是乳腺癌最常见的影像学特征。但由于乳腺组织中的腺体、结缔组织、血管、脂肪等软组织的密度与病灶区域的密度都很接近,诊断者的视觉疲劳等因素,使得早期癌症的误诊和漏诊仍时常发生。随着计算机技术和数字图像处理技术的飞速发展,使得利用计算机进行乳腺微钙化点辅助检测成为可能。利用数字图像处理技术对乳腺X线图像中的微钙化点进行增强处理,并对病灶区域进行标记,可以将医生从繁琐的阅片、分类工作中解脱出来,帮助医生对图像进行更好的理解和判断,从而降低误诊与漏诊,达到提高诊断正确率的目的。At present, the main method used in the diagnosis of breast cancer is mammography soft X-ray examination, in which microcalcifications and masses are the most common imaging features of breast cancer. However, because the density of soft tissue such as glands, connective tissue, blood vessels, and fat in breast tissue is very close to the density of the lesion area, and the visual fatigue of the diagnostician and other factors, misdiagnosis and missed diagnosis of early cancer still often occur. With the rapid development of computer technology and digital image processing technology, it is possible to use computer to assist detection of breast microcalcifications. Using digital image processing technology to enhance the microcalcifications in mammography images and mark the lesion area can free doctors from the tedious work of reading and classifying images, and help doctors better understand the images and judgment, so as to reduce misdiagnosis and missed diagnosis, and achieve the purpose of improving the correct rate of diagnosis.

但是目前使用的方法在微钙化点自动检测方面存在着以下几点问题:首先,现有的检测方法一般都存在着检测效果不够理想,检测算法的稳定性不高,特别是在一些乳腺组织致密、图像质量较低的图像中,微钙化点目标难以检测出来的现象严重;其次,存在着对微钙化点病灶区域提取不够充分或者提取的病灶区域过大等缺点,给后续的特征提取造成了很大的困难;最后,采用什么样的特征和分类器对微钙化点区域进行描述和分类,才能使得阳性样本的检测准确率最高,一直没有得到很好的解决。However, the currently used methods have the following problems in the automatic detection of micro-calcification points: First, the existing detection methods generally have unsatisfactory detection results, and the stability of the detection algorithm is not high, especially in some dense breast tissues. 1. In images with low image quality, it is difficult to detect the micro-calcification target; secondly, there are shortcomings such as insufficient extraction of the micro-calcification lesion area or too large extracted lesion area, which causes subsequent feature extraction. It is very difficult; finally, what kind of features and classifiers to use to describe and classify the microcalcification area can make the detection accuracy of positive samples the highest, and it has not been well resolved.

发明内容Contents of the invention

本发明的目的是提供一种乳腺微钙化点计算机辅助检测方法,解决了现有技术中存在的对致密乳腺X线图像中微钙化点目标难以完全正确检出、检测结果假阳性率过高的问题。The purpose of the present invention is to provide a computer-aided detection method for breast microcalcifications, which solves the problems in the prior art that it is difficult to completely and correctly detect microcalcifications in dense mammograms and the false positive rate of detection results is too high question.

本发明采用的技术方案为,一种乳腺微钙化点自动检测的方法,包括以下操作步骤:The technical scheme adopted in the present invention is a method for automatic detection of breast microcalcifications, comprising the following steps:

步骤1,对原始乳腺图像进行灰度校正,以提高图像的整体对比度,得到灰度校正后的图像F(x,y);Step 1, perform grayscale correction on the original mammary gland image to improve the overall contrast of the image, and obtain the image F(x, y) after grayscale correction;

步骤2,对灰度校正后的图像中疑似微钙化点目标区域的中心位置细节和边缘区域细节进行增强,然后将增强后的疑似微钙化点目标区域叠加到灰度校正后的图像上,得到微钙化点增强的乳腺图像F1(x,y);Step 2: Enhance the center position details and edge area details of the suspected microcalcification target area in the grayscale corrected image, and then superimpose the enhanced suspected microcalcification target area on the grayscale corrected image to obtain Microcalcification-enhanced breast image F 1 (x, y);

步骤3,选用比钙化点目标略大的圆形结构元素,对灰度校正后的图像进行Top-hat变换,得到背景抑制后的乳腺图像F2(x,y);Step 3, select a circular structural element slightly larger than the calcification point target, perform Top-hat transformation on the image after grayscale correction, and obtain the breast image F 2 (x, y) after background suppression;

步骤4,对上述步骤2所得的图像F1(x,y)和步骤3所得的图像F2(x,y)联合阈值T1和阈值T2进行双阈值分割,其中,阈值T1为图像F1(x,y)最大灰度的85%,阈值T2为图像F2(x,y)最大灰度的80%;双阈值分割后形成的目标点作为初步检测出的疑似微钙化点目标区域;然后去掉部分虚假钙化点目标区,完成钙化点目标区的粗检;Step 4, perform dual-threshold segmentation on the image F 1 (x, y) obtained in the above step 2 and the image F 2 (x, y) obtained in the step 3 jointly with the threshold T 1 and the threshold T 2 , where the threshold T 1 is the image 85% of the maximum gray level of F 1 (x, y), and the threshold T 2 is 80% of the maximum gray level of image F 2 (x, y); the target points formed after the double-threshold segmentation are used as suspected microcalcification points initially detected target area; then remove part of the false calcification point target area, and complete the rough inspection of the calcification point target area;

步骤5,针对步骤4粗检出的每一个微钙化点目标区,在原始乳腺图像对应的位置提取每一个目标区的圆形度、对比度、均值及方差组成的4维特征向量;Step 5, for each microcalcification target area roughly detected in step 4, extract a 4-dimensional feature vector consisting of circularity, contrast, mean and variance of each target area at the position corresponding to the original breast image;

步骤6,将提取到的4维特征向量,交由SVM分类器进行判断,判断粗检出的微钙化点是否为真实的微钙化点目标区;Step 6, submit the extracted 4-dimensional feature vector to the SVM classifier for judgment, and judge whether the roughly detected microcalcification point is the real microcalcification point target area;

步骤7,对判断认为是真实的微钙化点目标区,将其标记到原始乳腺图像上,即完成对乳腺微钙化点的自动检测。Step 7: mark the microcalcification point target area that is judged to be real on the original mammary gland image, that is, complete the automatic detection of mammary gland microcalcification point.

本发明的有益效果是,1.本发明对质量不高的乳腺图像中的微钙化点检测时,能够准确的检测出图像中的微钙化点且假阳性区域很少,提高了检测的精度。2.可以将医生从繁琐的阅片、分类工作中解脱出来,减轻医生的工作量,提高检测的自动化程度和检测的速度。The beneficial effects of the present invention are: 1. When the present invention detects microcalcifications in low-quality mammary gland images, it can accurately detect microcalcifications in the image and there are few false positive areas, which improves the detection accuracy. 2. It can free doctors from the tedious work of image reading and classification, reduce the workload of doctors, and improve the automation and speed of detection.

附图说明Description of drawings

图1是本发明检测方法的流程图;Fig. 1 is the flowchart of detection method of the present invention;

图2是本发明实施例步骤1中一幅带有微钙化点的原始乳腺图像;Fig. 2 is an original mammary gland image with microcalcifications in step 1 of the embodiment of the present invention;

图3是本发明实施例步骤1中Gamma变换校正后的图像;Fig. 3 is the image after Gamma transform correction in step 1 of the embodiment of the present invention;

图4是本发明实施例步骤2中采用双结构元素,进行微钙化点增强后的图像;Fig. 4 is the image after micro-calcification point enhancement using double structural elements in step 2 of the embodiment of the present invention;

图5是本发明实施例步骤3中经过Top-hat变换后的图像;Fig. 5 is the image after Top-hat transformation in step 3 of the embodiment of the present invention;

图6是本发明实施例步骤4中双阈值分割后的二值图像;Fig. 6 is the binary image after the double-threshold segmentation in step 4 of the embodiment of the present invention;

图7是本发明实施例步骤4中经过后处理后的二值图像;Fig. 7 is the binary image after post-processing in step 4 of the embodiment of the present invention;

图8是本发明实施例步骤7中分类后标记出的微钙化点图像。Fig. 8 is an image of microcalcifications marked after classification in step 7 of the embodiment of the present invention.

具体实施方式Detailed ways

下面通过具体实施方式对本发明进行详细说明。The present invention will be described in detail below through specific embodiments.

如图1所示,本发明所提供的一种乳腺微钙化点计算机辅助检测方法,包括以下操作步骤:As shown in Figure 1, a kind of breast microcalcification point computer aided detection method provided by the present invention comprises the following steps:

步骤1,因为原始乳腺X线图像整体对比度不高,所以采用Gamma灰度校正的方法对原始乳腺图像进行灰度校正,以提高图像的整体对比度;Step 1, because the overall contrast of the original mammogram image is not high, so the Gamma gray scale correction method is used to perform gray scale correction on the original breast image to improve the overall contrast of the image;

所述Gamma灰度校正的方法为:

Figure GSA00000031206300041
其中I(x,y)为输入的原始乳腺图像,F(x,y)为Gamma灰度校正后的图像,γ为Gamma值;The method of Gamma gray scale correction is:
Figure GSA00000031206300041
Wherein I(x, y) is the input original mammary image, F(x, y) is the image after Gamma grayscale correction, and γ is the Gamma value;

步骤2,因为微钙化点在图像中多呈现出近圆形、面积较小的特征,采用双结构元素,通过形态学中灰度梯度运算,增强灰度校正后图像F(x,y)中疑似微钙化点目标区域的中心位置细节和边缘区域细节,然后将增强后的疑似微钙化点目标区域叠加到灰度校正后的图像F(x,y)上,得到微钙化点增强的乳腺图像F1(x,y),便于检测钙化点;其具体方法为:Step 2, because the micro-calcification points in the image usually present the characteristics of a near-circular shape and a small area, using dual structural elements, through the gray-scale gradient operation in the morphology, to enhance the gray-scale corrected image F(x, y) The center position details and edge area details of the suspected microcalcification target area, and then the enhanced suspected microcalcification target area is superimposed on the grayscale corrected image F(x, y) to obtain a microcalcification enhanced breast image F 1 (x, y) is convenient for detecting calcification points; the specific method is:

1)利用双结构元素为

Figure GSA00000031206300042
Figure GSA00000031206300043
其中,B1为内中心对称结构,用于强化靠近目标中心位置的细节;B2为外中心对称结构,用于强化目标边缘区域的细节;1) Utilize the double structuring element as
Figure GSA00000031206300042
and
Figure GSA00000031206300043
Among them, B 1 is an inner centrosymmetric structure, which is used to enhance the details near the center of the target; B 2 is an outer centrosymmetric structure, which is used to enhance the details of the target edge area;

2)利用结构元素B1,对Gamma灰度校正后的图像F(x,y)进行灰度形态学梯度运算得到图像G1(x,y),即

Figure GSA00000031206300044
2) Using the structural element B 1 , perform the gray-scale morphological gradient operation on the image F(x, y) after Gamma gray-scale correction to obtain the image G 1 (x, y), namely
Figure GSA00000031206300044

3)利用结构元素B2,对Gamma灰度校正后的图像F(x,y)进行灰度形态学梯度运算得到图像G2(x,y),即

Figure GSA00000031206300051
3) Using the structural element B 2 , perform the gray-scale morphological gradient operation on the image F(x, y) after Gamma gray-scale correction to obtain the image G 2 (x, y), namely
Figure GSA00000031206300051

4)将形成的图像G1(x,y)和G2(x,y)叠加到Gamma灰度校正后的图像F(x,y)上,形成微钙化点增强后的乳腺图像F1(x,y),即:F1(x,y)=F(x,y)+G1(x,y)+G2(x,y);4) Superimpose the formed images G 1 (x, y) and G 2 (x, y) on the Gamma-corrected image F (x, y) to form a breast image F 1 ( x, y), namely: F 1 (x, y) = F (x, y) + G 1 (x, y) + G 2 (x, y);

步骤3,为了进一步突出钙化点目标区域,抑制乳腺组织背景的影响,选用比钙化点目标略大的圆形结构元素,对Gamma校正后的图像进行Top-hat变换,得到背景抑制后的乳腺图像,其中的微钙化点目标区域初步显现出来;其具体方法为:Step 3: In order to further highlight the calcification point target area and suppress the influence of the breast tissue background, select a circular structural element slightly larger than the calcification point target, and perform Top-hat transformation on the Gamma-corrected image to obtain the background-suppressed breast image , in which the target area of microcalcification point appears initially; the specific method is:

1)利用圆形结构元素

Figure GSA00000031206300052
1) Utilize circular structural elements
Figure GSA00000031206300052

2)对Gamma灰度校正后的图像F(x,y)进行形态学Top-hat变换,形成背景抑制的乳腺图像F2(x,y),即F2(x,y)=F(x,y)-(F(x,y)оB3(x,y));2) Perform morphological Top-hat transformation on the image F(x, y) after Gamma grayscale correction to form a background-suppressed breast image F 2 (x, y), that is, F 2 (x, y)=F(x ,y)-(F(x,y)оB 3 (x,y));

步骤4,步骤2得到的图像中,对微钙化点目标区域增强的同时,也对背景中与微钙化点目标形状特性接近的区域进行了增强,造成了“噪声干扰区域”;而步骤3得到的图像中,背景则被很好地抑制了。为此,对步骤2和步骤3中得到的两幅图像分别采用不同的阈值,联合进行分割,形成的目标点作为初步的钙化点目标区;进一步,考虑到微钙化点目标的大小及分布范围限制,然后进行后处理,去掉部分虚假的钙化点目标区,完成钙化点目标区的粗检;其具体方法为;In step 4, in the image obtained in step 2, while enhancing the microcalcification target area, the area in the background that is close to the microcalcification target shape characteristics is also enhanced, resulting in a "noise interference area"; and step 3 is obtained In the image, the background is well suppressed. To this end, the two images obtained in step 2 and step 3 are separately segmented using different thresholds, and the formed target point is used as the preliminary calcification point target area; further, considering the size and distribution range of the micro-calcification point target Limit, and then perform post-processing to remove part of the false calcification point target area, and complete the rough inspection of the calcification point target area; the specific method is;

1)经过多次试验统计数据得到,将步骤2得到的图像F1(x,y)的最大灰度的85%设为阈值T1,将步骤3得到的图像F2(x,y)的最大灰度的80%设为阈值T21) Obtained through statistical data of many experiments, set 85% of the maximum grayscale of the image F 1 (x, y) obtained in step 2 as the threshold T 1 , and set the threshold T 1 of the image F 2 (x, y) obtained in step 3 80% of the maximum gray scale is set as the threshold T 2 ;

2)再对图像F1(x,y)和图像F2(x,y)联合阈值T1和阈值T2进行双阈值分割,即对同时满足条件:F1(x,y)>T1且F2(x,y)>T2的像素点即被确定为初步检测出来的疑似微钙化点目标区域;2) Carry out double-threshold segmentation on image F 1 (x, y) and image F 2 (x, y) jointly with threshold T 1 and threshold T 2 , that is, to satisfy the condition at the same time: F 1 (x, y) > T 1 And the pixel points with F 2 (x, y)>T 2 are determined as the target areas of suspected microcalcifications initially detected;

3)最后去除面积小于2个像素或者大于20个像素目标区域,去除图像中位于上下左右边界附近的目标区域,形成粗检出的微钙化点目标区域;3) Finally, remove the target area with an area smaller than 2 pixels or larger than 20 pixels, remove the target area near the upper, lower, left, and right boundaries in the image, and form a roughly detected micro-calcification target area;

步骤5,在步骤4中粗检出的钙化点目标图像中,含有许多的虚假的钙化点目标,称为假阳性区。为进一步去除掉这些假阳性区,在原始乳腺图像上提取步骤4粗检出的每一个钙化点目标区的圆形度、对比度、均值及方差,将其作为钙化点目标区域的典型特征,组成4维特征向量;提取的4维特征向量为:Step 5, in the coarsely detected calcification point target image in step 4, there are many false calcification point targets, which are called false positive regions. In order to further remove these false positive areas, extract the circularity, contrast, mean and variance of each calcification target area roughly detected in step 4 on the original breast image, and use it as the typical feature of the calcification target area, consisting of 4-dimensional feature vector; the extracted 4-dimensional feature vector is:

1)目标区域圆形度:Y=P2/(4πS),其中,P是目标区域的周长,S为目标区域的面积;1) Circularity of the target area: Y=P 2 /(4πS), where P is the perimeter of the target area, and S is the area of the target area;

2)目标区域对比度:

Figure GSA00000031206300061
其中f和b分别表示目标区域和背景区域的平均灰度,具体为:其中Nf表示粗检出的一个微钙化点目标区域的像素个数,Ωf表示粗检出的一个微钙化点目标区像素组成的集合;
Figure GSA00000031206300063
其中Ωb表示包围微钙化点的外界矩形区域中非微钙化点组成的像素集合,而外界矩形区域是由包含一个微钙化点目标区的最小外接矩形分别向上、下、左、右各外扩一个像素组成的区域,Nb表示Ωb中的像素个数;2) Target area contrast:
Figure GSA00000031206300061
where f and b represent the average grayscale of the target area and the background area, respectively, specifically: Wherein N f represents the number of pixels of a microcalcification target area detected roughly, and Ω f represents a set of pixels in a micro calcification target area detected roughly;
Figure GSA00000031206300063
Among them, Ω b represents the pixel set composed of non-micro-calcification points in the outer rectangular area surrounding the micro-calcification point, and the outer rectangular area is expanded upward, downward, left, and right respectively by the smallest circumscribed rectangle containing a micro-calcification point target area. An area composed of one pixel, N b represents the number of pixels in Ω b ;

3)目标区域均值:

Figure GSA00000031206300071
其中Nf表示粗检出的一个微钙化点目标区域的像素个数,Ωf表示粗检出的一个微钙化点目标区像素组成的集合;3) Mean value of the target area:
Figure GSA00000031206300071
Wherein N f represents the number of pixels of a microcalcification target area detected roughly, and Ω f represents a set of pixels in a micro calcification target area detected roughly;

4)目标区域方差:

Figure GSA00000031206300072
其中Nf表示粗检出的一个微钙化点目标区域的像素个数,Ωf表示粗检出的一个微钙化点目标区像素组成的集合;4) Target area variance:
Figure GSA00000031206300072
Wherein N f represents the number of pixels of a microcalcification target area detected roughly, and Ω f represents a set of pixels in a micro calcification target area detected roughly;

步骤6,利用步骤5中提取出的特征向量,采用正样本和负样本,训练支持向量机;然后将提取粗检出的钙化点目标区的特征向量,输入到训练好的向量机中去,对该目标区进行分类,得到其是否是真实的钙化点目标区;Step 6, using the feature vector extracted in step 5, using positive samples and negative samples, to train the support vector machine; then extracting the feature vector of the rough detected calcification point target area and inputting it into the trained vector machine, Classifying the target area to obtain whether it is a real calcification point target area;

用支持向量机的方法,对粗检出的微钙化点目标区进行分类的方法为:Using the method of support vector machine, the method for classifying the target area of microcalcification point detected roughly is:

1)支持向量机中用到的核函数为高斯径向基核函数;1) The kernel function used in the support vector machine is a Gaussian radial basis kernel function;

2)对比标记的真实微钙化点区域,将粗检检测出来的微钙化点目标区分为正样本和负样本,将样本随机分成5个尺寸的子集,对每个模型参数集,训练SVM分类器;2) Compared with the marked real microcalcification area, the microcalcification target detected by rough inspection is divided into positive samples and negative samples, and the samples are randomly divided into 5 size subsets. For each model parameter set, SVM classification is trained device;

3)提取粗检出的微钙化点目标区的4维特征向量,用训练好的SVM分类器,对该目标进行分类,得出其是否是真实的微钙化点目标区;3) Extract the 4-dimensional feature vector of the microcalcification point target area that is roughly detected, and use the trained SVM classifier to classify the target to obtain whether it is a real microcalcification point target area;

步骤7,对判断认为是真实的微钙化点目标区,将其标记到原始的乳腺图像上,即完成对乳腺微钙化点的自动检测。Step 7: mark the target area of the microcalcification point that is judged to be real on the original mammary gland image, that is, complete the automatic detection of the microcalcification point of the mammary gland.

实施例1Example 1

一种乳腺微钙化点计算机辅助检测方法,通过以下步骤进行具体的实施:A method for computer-aided detection of mammary gland microcalcifications is implemented through the following steps:

步骤1,读取一幅如图2所示的原始乳腺图像,再采用Gamma灰度校正方法对原始乳腺图像进行灰度校正:Step 1, read an original mammary gland image as shown in Figure 2, and then use the Gamma grayscale correction method to perform grayscale correction on the original mammary gland image:

其Gamma灰度校正的方法为:其中I(x,y)为输入原始图像,F(x,y)为Gamma灰度校正后的图像,γ的取值为3,得到灰度校正后的图像如图3所示;The Gamma grayscale correction method is: Wherein I(x, y) is the input original image, F(x, y) is the image after Gamma grayscale correction, and the value of γ is 3, and the image after grayscale correction is obtained as shown in Figure 3;

步骤2,采用基于双结构元素的背景叠加方法,增强图3中疑似微钙化点目标区域的中心位置细节和边缘区域细节:Step 2, use the background overlay method based on double structural elements to enhance the center position details and edge area details of the suspected microcalcification target area in Figure 3:

运用双结构元素:

Figure GSA00000031206300082
Figure GSA00000031206300083
对图3进行下述形态学处理,得到图像G1(x,y)和G2(x,y):Using double structuring elements:
Figure GSA00000031206300082
and
Figure GSA00000031206300083
Perform the following morphological processing on Fig. 3 to obtain images G 1 (x, y) and G 2 (x, y):

GG 11 (( xx ,, ythe y )) == (( Ff (( xx ,, ythe y )) ⊕⊕ BB 11 (( xx ,, ythe y )) )) -- (( Ff (( xx ,, ythe y )) ΘΘ BB 11 (( xx ,, ythe y )) ))

GG 22 (( xx ,, ythe y )) == (( Ff (( xx ,, ythe y )) ⊕⊕ BB 22 (( xx ,, ythe y )) )) -- (( Ff (( xx ,, ythe y )) ΘΘ BB 22 (( xx ,, ythe y )) ))

然后,将图像G1(x,y)和G2(x,y)叠加到图3上,形成微钙化点增强后的乳腺图像F1(x,y),即:F1(x,y)=F(x,y)+G1(x,y)+G2(x,y),如图4所示;Then, images G 1 (x, y) and G 2 (x, y) are superimposed on Fig. 3 to form a breast image F 1 (x, y) enhanced by microcalcifications, namely: F 1 (x, y )=F(x, y)+G 1 (x, y)+G 2 (x, y), as shown in Figure 4;

步骤3,运用形态学中的Top-hat变换,形成背景抑制后的乳腺图像:运用结构元素

Figure GSA00000031206300086
对图3进行Top-hat变换,得到如图5所示背景抑制后的乳腺图像F2(x,y),即F2(x,y)=F(x,y)-(F(x,y)оB3(x,y));Step 3, use the Top-hat transformation in morphology to form a breast image after background suppression: use structural elements
Figure GSA00000031206300086
Perform Top-hat transformation on Fig. 3 to obtain the breast image F 2 (x, y) after background suppression as shown in Fig. 5 , that is, F 2 (x, y)=F(x, y)-(F(x, y) о B 3 (x, y));

步骤4,采用双阈值及后处理的方法,粗检出微钙化点目标区域:Step 4, use the method of double threshold and post-processing to roughly detect the target area of microcalcification points:

选择阈值T1为图4所示图像最大灰度的85%,阈值T2为图5所示图像最大灰度的80%,分别对图4所示图像(微钙化点增强后的图象)和图5所示图像(Top-hat变换后的图像)联合阈值T1和阈值T2进行双阈值分割,得到双阈值分割后的二值图像,如图6所示,是初步检测出的疑似微钙化点目标区;最后,对图6中面积小于2个像素或者大于20个像素目标区域,以及位于上下左右边界附近的目标区域,进行去除,形成粗检出的微钙化点目标区域,如图7所示;Select threshold T1 to be 85% of the maximum gray scale of the image shown in Figure 4, and threshold T2 to be 80% of the maximum gray scale of the image shown in Figure 5, respectively for the image shown in Figure 4 (the image after the enhancement of microcalcification points) and the image shown in Figure 5 (image after Top-hat transformation) combined with threshold T 1 and threshold T 2 to perform dual-threshold segmentation to obtain a binary image after dual-threshold segmentation, as shown in Figure 6, which is the suspected Microcalcification target area; finally, remove the target area with an area of less than 2 pixels or greater than 20 pixels, and the target area near the upper, lower, left, and right boundaries in Figure 6 to form a coarsely detected microcalcification target area, such as As shown in Figure 7;

步骤5,针对图7中粗检出的每一个微钙化点目标区,在图2对应的位置提取每一个目标区的圆形度、对比度、直方图均值及直方图方差4维特征向量:Step 5, for each microcalcification point target area roughly detected in Figure 7, extract the circularity, contrast, histogram mean and histogram variance 4-dimensional feature vector of each target area at the corresponding position in Figure 2:

1)目标区域圆形度:Y=P2/(4πS),其中P是目标区域的周长,S为目标区域的面积;1) Circularity of the target area: Y=P 2 /(4πS), where P is the perimeter of the target area, and S is the area of the target area;

2)目标区域对比度:

Figure GSA00000031206300091
其中f和b分别表示目标区域和背景区域的平均灰度,具体为:
Figure GSA00000031206300092
其中Nf表示粗检出的一个微钙化点目标区域的像素个数,Ωf表示粗检出的一个微钙化点目标区像素组成的集合;其中Ωb表示包围微钙化点的外界矩形区域中非微钙化点组成的像素集合,而外界矩形区域是由包含一个微钙化点目标区的最小外接矩形分别向上、下、左、右各外扩一个像素组成的区域,Nb表示Ωb中的像素个数;2) Target area contrast:
Figure GSA00000031206300091
where f and b represent the average grayscale of the target area and the background area, respectively, specifically:
Figure GSA00000031206300092
Wherein N f represents the number of pixels of a microcalcification target area detected roughly, and Ω f represents a set of pixels in a micro calcification target area detected roughly; Among them, Ω b represents the pixel set composed of non-micro-calcification points in the outer rectangular area surrounding the micro-calcification point, and the outer rectangular area is expanded upward, downward, left, and right respectively by the smallest circumscribed rectangle containing a micro-calcification point target area. An area composed of one pixel, N b represents the number of pixels in Ω b ;

3)目标区域均值:

Figure GSA00000031206300094
其中Nf表示粗检出的一个微钙化点目标区域的像素个数,Ωf表示粗检出的一个微钙化点目标区像素组成的集合;3) Mean value of the target area:
Figure GSA00000031206300094
Wherein N f represents the number of pixels of a microcalcification target area detected roughly, and Ω f represents a set of pixels in a micro calcification target area detected roughly;

4)目标区域方差:

Figure GSA00000031206300101
其中Nf表示粗检出的一个微钙化点目标区域的像素个数,Ωf表示粗检出的一个微钙化点目标区像素组成的集合;4) Target area variance:
Figure GSA00000031206300101
Wherein N f represents the number of pixels of a microcalcification target area detected roughly, and Ω f represents a set of pixels in a micro calcification target area detected roughly;

步骤6,采用支持向量机的方法,对粗检出的微钙化点目标区进行分类:对图7中的每一个微钙化点目标区提取到的4维特征向量,交由SVM分类器进行判断,得到其是否是真实的微钙化点目标区;Step 6, using the support vector machine method to classify the coarsely detected microcalcification target area: the 4-dimensional feature vector extracted from each microcalcification target area in Figure 7 is handed over to the SVM classifier for judgment , to get whether it is the real microcalcification target area;

步骤7,对判断认为是真实的微钙化点目标区,将其标记到原始的乳腺图像图2上,标记的结果如图8所示,即完成对乳腺微钙化点的自动检测。Step 7: mark the microcalcification target area that is judged to be real on the original mammary image in Figure 2, and the marking result is shown in Figure 8, that is, the automatic detection of breast microcalcification is completed.

Claims (6)

1. the method that the mammary gland microcalcifications detects automatically is characterized in that, comprises following operation steps:
Step 1 is carried out gray correction to original galactophore image, to improve the overall contrast of image, obtain after the gray correction image F (x, y);
Step 2, center details and fringe region details to doubtful microcalcifications target area in the image after the gray correction strengthen, doubtful microcalcifications target area after will strengthening then is added on the image after the gray correction, obtains the galactophore image F that microcalcifications strengthens 1(x, y);
Step 3 is selected the circular configuration element more bigger than calcification point target for use, and the image after the gray correction is carried out the Top-hat conversion, obtains the galactophore image F after background suppresses 2(x, y);
Step 4 is to the image F of above-mentioned steps 2 gained 1(x, y) and the image F of step 3 gained 2(x, y) associating threshold value T 1With threshold value T 2Carry out dual threshold and cut apart, wherein, threshold value T 1Be image F 1(x, y) 85% of maximum gray scale, threshold value T 2Be image F 2(x, y) 80% of maximum gray scale; The doubtful microcalcifications target area that the impact point that forms after dual threshold is cut apart goes out as Preliminary detection; Remove the false calcification point of part target area then, finish the Rough Inspection of calcification point target area;
Step 5, each microcalcifications target area that Rough Inspection goes out at step 4 extracts the circularity, contrast, average of each target area and 4 dimensional feature vectors that variance is formed in the position of original galactophore image correspondence;
Step 6 with 4 dimensional feature vectors that extract, is transferred to the svm classifier device and is judged, judges whether the microcalcifications that Rough Inspection goes out is real microcalcifications target area;
Step 7 is thought real microcalcifications target area to judgement, and its mark to original galactophore image, is promptly finished the automatic detection to the mammary gland microcalcifications.
2. the method that a kind of mammary gland microcalcifications according to claim 1 detects automatically is characterized in that the concrete operations step of described step 1 is:
Adopt Gamma gray correction method that original galactophore image is carried out gray correction, to improve the overall contrast of image;
Described Gamma gray correction method is:
Figure FSA00000031206200021
Wherein (x y) is the original galactophore image of input to I, and (x y) is the image after the gray correction to F, and γ is the Gamma value.
3. the method that a kind of mammary gland microcalcifications according to claim 1 detects automatically is characterized in that the concrete operations step of described step 2 is:
Adopt the double structure element, by shade of gray computing in the morphology, to the image F (x after the gray correction, y) the center details of doubtful microcalcifications target area and fringe region details strengthen in, doubtful microcalcifications target area after will strengthening the then image F (x after the gray correction that is added to, y) on, obtain the galactophore image F that microcalcifications strengthens 1(x, y); Its concrete grammar is:
1) adopts the double structure element
Figure FSA00000031206200022
And
Figure FSA00000031206200023
Wherein, B 1Be interior centrosymmetric structure, be used to strengthen details, B near the target's center position 2Be outer centrosymmetric structure, be used to strengthen the details in object edge zone;
2) utilize structural element B 1, (x y) carries out the computing of gray scale morphology gradient and obtains image G to the image F after the gray correction 1(x, y), promptly
Figure FSA00000031206200024
3) utilize structural element B 2, (x y) carries out the computing of gray scale morphology gradient and obtains image G to the image F after the gray correction 2(x, y), promptly
Figure FSA00000031206200025
4) with the image G that forms 1(x, y) and G 2(x, y) be added to image F after the gray correction (x, y) on, form the galactophore image F after microcalcifications strengthens 1(x, y), that is: F 1(x, y)=F (x, y)+G 1(x, y)+G 2(x, y).
4. the method that a kind of mammary gland microcalcifications according to claim 1 detects automatically is characterized in that the concrete operations step of described step 3:
The circular configuration element that utilization is more bigger than calcification point target carries out the Top-hat conversion to the image after the gray correction, obtains the galactophore image F after background suppresses 2(x, y), microcalcifications target area wherein tentatively displays; Its concrete grammar is:
1) selects the circular configuration element for use B 3 = 0 0 1 0 0 0 1 1 1 0 1 1 1 1 1 0 1 1 1 0 0 0 1 0 0 ;
2) (x y) carries out morphology Top-hat conversion, forms the galactophore image F that background suppresses to the image F after the gray correction 2(x, y), i.e. F 2(x, y)=F (x, y)-(F (x, y) о B 3(x, y)).
5. the method that a kind of mammary gland microcalcifications according to claim 1 detects automatically is characterized in that the concrete operations step of described step 4:
Two width of cloth images that obtain in step 2 and the step 3 are adopted different threshold values respectively, unite and cut apart, the impact point of formation removes the calcification point target area of part falseness then as preliminary calcification point target area, finishes the Rough Inspection of calcification point target area; Its concrete grammar is:
1) the image F that obtains for step 2 1(x, y), with image F 1(x y) 85% of maximum gray scale is made as threshold value T 1The image F that obtains for step 3 2(x, y), with image F 2(x y) 80% of maximum gray scale is made as threshold value T 2
2) again to image F 1(x is y) with image F 2(x, y) associating threshold value T 1With threshold value T 2Carry out dual threshold and cut apart, promptly satisfy T simultaneously 1(x, y)>T 1And T 2(x, y)>T 2The doubtful microcalcifications target area that goes out as Preliminary detection of pixel;
3) remove area at last less than 2 pixels or greater than 20 pixel target areas, be positioned at the target area of boundary vicinity up and down in the removal image, form the microcalcifications target area that Rough Inspection goes out.
6. the method that a kind of mammary gland microcalcifications according to claim 1 detects automatically is characterized in that the concrete operations step of described step 5:
Each calcification point target area that Rough Inspection goes out at step 4 extracts circularity, contrast, average and the variance of each target area in the position of original galactophore image correspondence, with its characteristic feature as the calcification point target area, form 4 dimensional feature vectors; 4 dimensional feature vectors that extract are:
1) target area circularity: Y=P 2/ (4 π S), wherein, P is the girth of target area, S is the area of target area;
2) target area contrast:
Figure FSA00000031206200041
Wherein f and b represent the average gray of target area and background area respectively; Be specially:
Figure FSA00000031206200042
N wherein fThe number of pixels of the microcalcifications target area that the expression Rough Inspection goes out, Ω fThe set that microcalcifications target area pixel is formed that the expression Rough Inspection goes out;
Figure FSA00000031206200043
Ω wherein bThe collection of pixels that non-microcalcifications is formed in the extraneous rectangular area of microcalcifications is surrounded in expression, and extraneous rectangular area by the minimum boundary rectangle that comprises a microcalcifications target area respectively up and down, the left and right zone that a pixel is formed, the N of respectively extending out bExpression Ω bIn number of pixels;
3) target area average:
Figure FSA00000031206200044
N wherein fThe number of pixels of the microcalcifications target area that the expression Rough Inspection goes out, Ω fThe set that microcalcifications target area pixel is formed that the expression Rough Inspection goes out;
4) target area variance: N wherein fThe number of pixels of the microcalcifications target area that the expression Rough Inspection goes out, Ω fThe set that microcalcifications target area pixel is formed that the expression Rough Inspection goes out.
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