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Computer-Aided Diagnosis of Soft-Tissue Tumors Using Sonographic Morphologic and Texture Features

Rationale and Objectives

The aim of this study was to develop a computer-aided diagnosis (CAD) system in assessing the sonographic morphologic and texture features of soft-tissue tumors.

Materials and Methods

The retrospective study involved 114 pathology proven cases including 73 benign and 41 malignant soft-tissue tumors. The tumor regions were delineated by an experienced radiologist who was unknown to the pathologic result. Then, we applied 10 morphologic features and 6 gray-level co-occurrence matrix texture features to analyze the tumor regions. To classify the tumors as benign or malignant, we used two methods, a linear discriminant analysis with stepwise feature selection and a multilayer neural network with the back-propagation algorithm as classifiers. The classification performances are evaluated by the area A z under the receiver operating characteristic. Furthermore, four radiologists provided malignancy grades for all tumors in the comparison of the CAD system.

Results

In this analysis, the CAD system based on the combination of morphologic and texture feature sets can give the optimal CAD result by LDA with an accuracy of 89.5%, a sensitivity of 90.2%, a specificity of 89.0%, a positive predictive value (PPV) of 82.2%, negative predictive value (NPV) of 94.2%, and A z value of 0.96, and by the multilayer perception with an accuracy of 88.6%, a sensitivity of 90.2%, a specificity of 87.5%, a positive predictive value of 80.4%, negative predictive value of 94.2%, and A z value of 0.95. The A z values of the four radiologists were ranged between 0.74 and 0.86, and the optimal CAD results were shown the highest A z values than the four radiologists’ rankings.

Conclusions

This study has shown that performing the CAD system with both morphologic and texture features on sonography, can successfully distinguish between benign and malignant soft-tissue tumors. Moreover, it can also provide a second opinion for the tumor diagnosis and avert unnecessary biopsy.

Soft-tissue tumors, which can arise anywhere in the body, occur in the extremities about two-thirds of the time and the other one-third of the time in the trunk, retroperitoneum, abdomen, or other locations . Malignant soft-tissue tumors, which have more than 50 histologic subtypes, constitute less than 1% of all cancers. Moreover, the overall survival of malignant soft-tissue tumors is about 50% at 5 years . The high death rate may be due to the lack of accurate diagnosis in early stages because such tumors usually grow without specific symptoms and pains. In addition, certain soft-tissue tumors have similar appearances between benignancy and malignancy; this phenomenon frequently leads to the delayed diagnosis without adequate initial management . If malignant tumors can be diagnosed correctly, patients’ survival rate will be increased .

Several imaging modalities have been used to assess soft-tissue tumors, with sonography being the preferred first-line screening tool in the clinic because of its advantages of low cost, nonionizing radiation, and real-time imaging. But some reports have indicated that sonography is limited to the differentiation between cysts and solid masses . Moreover, the sonographic examination relies heavily on the radiologists’ experience, so the reproducibility is hard to maintain among different measures. Fortunately, improvements in ultrasound technology have enabled the fine anatomic structures of tumors to be visualized in recent years .

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Materials and methods

Database Acquisition

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Feature Extraction

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Morphologic features

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Circularity=4π×AreaPerimeter2 C

i

r

c

u

l

a

r

i

t

y

=

4

π

×

A

r

e

a

P

e

r

i

m

e

t

e

r

2

where perimeter is the length of the tumor’s perimeter. Circularity can show the extent of a tumor approaching to a circle. If the value of circularity is close to 1, the tumor shape should be near regularity. Get Radiology Tree app to read full this article<

Compactness=Area∩AreaeqArea C

o

mpactness

=

A

r

e

a

A

r

e

a

e

q

A

r

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a

where Area eq is an equivalent circle of the tumor area. If the ratio is close to 1, a tumor would be approaching the uniformity. Get Radiology Tree app to read full this article<

Eccentricity=a2−b2√a E

c

c

e

n

t

r

i

c

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t

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=

a

2

b

2

a

where a and b represent the major and minor axes of the equivalent ellipse. Figure 1, Characteristic of eccentricity in (a) a benign and (b) a malignant tumor.

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ENC=Ellipseeq_PerimeterPerimeter E

N

C

=

E

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l

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p

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e

eq

_

P

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r

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m

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t

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where Ellipse eq _Perimeter denotes the perimeter of the equivalent ellipse. When ENC is close to 1, the tumor boundary exhibited slight lobulations and smooth shape. Get Radiology Tree app to read full this article<

EAR=Area∩EllipseeqArea E

AR

=

A

r

e

a

E

l

l

i

p

s

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e

q

A

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a

where Ellipse eq is the equivalent ellipse of the tumor. The feature is similar to compactness. When EAR is close to 0, the tumor has a high probability of being malignant. Get Radiology Tree app to read full this article<

Roundness=4×Areaπ×Max_Diameter2 R

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u

n

d

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s

=

4

×

A

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π

×

M

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_

D

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where Max_Diameter is measured with the length of the major axis from the equivalent ellipse of a tumor. Get Radiology Tree app to read full this article<

Figure 2, Subimage of a malignant tumor with convex points (solid points) and concave points (open points) . Solid line indicates the tumor margin; dashed line indicates the connection of the concave points.

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Li=Amax−AminAavg L

i

=

A

max

A

min

A

a

v

g

where A max and A min denote the sizes of the largest and the smallest lobulations, and A avg indicates the average size of all lobulations. The measure of a malignant tumor usually accompany with a larger LI value. Get Radiology Tree app to read full this article<

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Texture features

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Table 1

The Pixel Resolutions of the Sonography under the Different Scan Widths by Depths

Sonography (Width × Depth) Resolution (mm/pixel) 4 cm × 3 cm 0.08 4 cm × 4 cm 0.10 4 cm × 5 cm 0.12 4 cm × 6 cm 0.15

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Classification Method

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Radiologists’ Rankings

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Results

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Table 2

Database of Different Histologic Subtypes with their Corresponding Amount and Misdiagnosis Numbers of Soft-tissue Tumors

Benign tumor Number/Ma/Mb Malignant tumor Number/Ma/Mb Lipoma 18/3/4 Metastasis tumor 9/1/1 Schwannoma 11/1/1 Malignant fibrous histiocytoma 7/0/1 Giant cell tumor 9/0/2 Liposarcoma 6/0/0 Glomus tumor 9/1/0 Lymphoma 4/0/0 Hemangioma 6/1/1 Osteogenic sarcoma 4/0/0 Fibroma 5/0/0 Alveolar soft part sarcoma 3/1/1 Leiomyoma 5/1/1 Epithelioid sarcoma 3/2/1 Aneurysm 4/0/0 Hemangiopericytoma 2/0/0 Neurofibroma 4/1/0 Fibromyxoid sarcoma 1/0/0 Benign fibrous histiocytoma 1/0/0 Synovial sarcoma 1/0/0 Glomangioma 1/0/0 Dermatofibrosarcoma 1/0/0 Total number 73/8/9 41/4/4

Ma, misdiagnosis of the linear discriminant analysis classifier; Mb, misdiagnosis of the multilayer perception classifier.

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Figure 3, Linear discriminant analysis classification performances of receiver-operating characteristic curves for morphologic features (dotted line) , texture features (dashed line) , and combination of two feature sets (solid line) .

Figure 4, Multilayer perception classification performances of receiver-operating characteristic curves for morphologic features (dotted line) , texture features (dashed line) , and combination of two feature sets (solid line) .

Table 3

Optimal Classification Performances of Soft-tissue Tumor with LDA and MLP Classifiers

LDA MLP Benign Malignant Benign Malignant Pathology Benign 65 4 64 4 Malignant 8 37 9 37 Total number 73 41 73 41

LDA, linear discriminant analysis; MLP, multilayer perception.

Table 4

Optimal Results by LDA and MLP Methods for the Classification of Soft-tissue Tumors

Classifier Accuracy Sensitivity Specificity PPV NPV A z LDA 89.5% 90.2% 89.0% 82.2% 94.2% 0.96 MLP 88.6% 90.2% 87.5% 80.4% 94.2% 0.95

LDA, linear discriminant analysis; MLP, multilayer perception; PPV, positive predictive value; NPV, negative predictive value.

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Figure 5, Clinical evaluations with the four radiologists' rankings by using area under the receiver-operating characteristic curves.

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Discussion

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