Home Computer-aided Diagnosis of Focal Liver Lesions by Use of Physicians' Subjective Classification of Echogenic Patterns in Baseline and Contrast-enhanced Ultrasonography
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Computer-aided Diagnosis of Focal Liver Lesions by Use of Physicians' Subjective Classification of Echogenic Patterns in Baseline and Contrast-enhanced Ultrasonography

Rational and Objectives

To develop a computer-aided diagnostic (CAD) scheme for classifying focal liver lesions (FLLs) by use of physicians’ subjective classification of echogenic patterns of FLLs on baseline and contrast-enhanced ultrasonography (US).

Materials and Methods

A total of 137 hepatic lesions in 137 patients were evaluated with B-mode and NC100100 (Sonazoid)-enhanced pulse-inversion US; lesions included 74 hepatocellular carcinomas (HCCs) (23: well-differentiated, 36: moderately differentiated, 15: poorly differentiated HCCs), 33 liver metastases, and 30 liver hemangiomas. Three physicians evaluated single images at B-mode and arterial phases with a cine mode. Physicians were asked to classify each lesion into one of eight B-mode and one of eight enhancement patterns, but did not make a diagnosis. To classify five types of FLLs, we employed a decision tree model with four decision nodes and four artificial neural networks (ANNs). The results of the physicians’ pattern classifications were used successively for four different ANNs in making decisions at each of the decision nodes in the decision tree model.

Results

The classification accuracies for the 137 FLLs were 84.8% for metastasis, 93.3% for hemangioma, and 98.6% for all HCCs. In addition, the classification accuracies for histological differentiation types of HCCs were 65.2% for well-differentiated HCC, 41.7% for moderately differentiated HCC, and 80.0% for poorly differentiated HCC.

Conclusions

This CAD scheme has the potential to improve the diagnostic accuracy of liver lesions. However, the accuracy in the histologic differential diagnosis of HCC based on baseline and contrast-enhanced US is still limited.

In the diagnosis of focal liver lesions (FLLs) including hepatocellular carcinoma (HCC), liver metastases, hemangioma, and focal nodular hyperplasia (FNH), contrast-enhanced computed tomography (CT) and magnetic resonance imaging (MRI) have been employed more commonly than ultrasonography (US). However, the ultrasonographic equipment is less expensive and can be installed easily compared with CT and MRI. Therefore, US may become more popular in the future, especially in the developing countries. In addition, contrast-enhanced US (CEUS) with pulse-inversion (phase-inversion) imaging techniques has been applied for improvement of the diagnostic accuracy of FLLs. Recently, second-generation ultrasonographic contrast agents, such as DMP 115 (Definity; Lantheus Inc., MA) in Canada and BR 1 (SonoVue; Bracco, Milan, Italy) in Europe and China, have been applied in clinical practice. The agent NC100100 (Sonazoid; GE Healthcare, Oslo, Norway) has become clinically available since January 2007, in Japan ahead of other countries. Although the second-generation ultrasonographic contrast agents have not yet been applied in clinical practice for the diagnosis of FLLs in United States, CEUS with these agents are being widely used worldwide.

The problem with US, however, is a disparity in the diagnostic accuracy among institutions. Generally, US strongly depends on subjective aspect of the sonologist, compared to CT and MRI . Although this problem has not been so serious in so-called “high-volume centers,” where US is used routinely for the diagnosis of FLLs, the diagnostic accuracy in an institution where US is performed infrequently can be poorer than that in a “high-volume center.” For reducing this disparity as much as possible, the development of a computer-aided diagnosis (CAD) scheme for the classification of FLLs on CEUS has been attempted .

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Materials and methods

Patient Population

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Ultrasonographic Technique

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Observer study for Obtaining Subjective Classifications of Echogenic Patterns

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Figure 1, (a) Illustration of morphologic patterns of hepatic tumors in the B-mode ultrasonography. (b) Illustration of enhancement patterns of hepatic tumors in the arterial phase.

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Computer-aided Diagnostic Scheme for the Classification of FLLs

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Figure 2, Illustration of the decision tree model used in this study. Four decision nodes in which alternative choice was determined by all five FLLs, leading to a final diagnostic decision for five liver lesions. D, decision node; FLL, focal liver lesion; HCC, hepatocellular carcinoma; LN, leaf node; m-HCC, moderately differentiated HCC; p-HCC, poorly differentiated HCC; w-HCC, well-differentiated HCC.

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Results

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Table 1

The Total Number of Lesions Rated by Three Readers for Subjective Classification of Eight Ultrasonographic Patterns of B-mode Imaging

Classification by Three Readers Lesion Number of Lesions Hyperechoic Hypoechoic Anechoic Thin Hypoechoic Rim Thick Hypoechoic Rim Hyperechoic Rim Mosaic Others HCC 74 18 (8%) 92 (41%) 0 (0%) 50 (23%) 4 (2%) 3 (1%) 44 (20%) 11 (5%) w-HCC 23 2 (3%) 42 (61%) 0 (0%) 9 (13%) 1 (1%) 1 (1%) 11 (16%) 3 (4%) m-HCC 36 11 (10%) 42 (39%) 0 (0%) 29 (27%) 2 (2%) 1 (1%) 17 (16%) 6 (6%) p-HCC 15 5 (11%) 8 (18%) 0 (0%) 12 (27%) 1 (2%) 1 (2%) 16 (36%) 2 (4%) Metastasis 33 16 (14%) 24 (24%) 2 (2%) 5 (5%) 42 (42%) 0 (0%) 3 (3%) 7 (7%) Hemangioma 30 37 (41%) 27 (30%) 0 (0%) 2 (2%) 0 (0%) 22 (24%) 2 (2%) 0 (0%)

Note. Numbers in parentheses are the percentage for the mean number of readers who rated the lesions for each pattern.

m-HCC, moderately differentiated hepatocellular carcinoma; p-HCC, poorly differentiated hepatocellular carcinoma; w-HCC, well-differentiated hepatocellular carcinoma.

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Table 2

The Total Number of Lesions Rated by Three Readers for Subjective Classification of Eight Ultrasonographic Patterns of Contrast Harmonic Imaging

Classification by Three Readers Lesion Number of Lesions Absent Dotted Peripheral Rimlike Peripheral Nodular Central with Spoke Wheel Shape Diffuse Homogeneous Diffuse Heterogeneous Others HCC 74 0 (0%) 0 (0%) 2 (1%) 19 (9%) 0 (0%) 104 (47%) 97 (44%) 0 (0%) w-HCC 23 0 (0%) 0 (0%) 0 (0%) 2 (3%) 0 (0%) 34 (49%) 33 (48%) 0 (0%) m-HCC 36 0 (0%) 0 (0%) 1 (1%) 6 (6%) 0 (0%) 69 (64%) 32 (30%) 0 (0%) p-HCC 15 0 (0%) 0 (0%) 1 (2%) 11 (24%) 0 (0%) 1 (2%) 32 (71%) 0 (0%) Metastasis 33 0 (0%) 0 (0%) 28 (28%) 40 (40%) 2 (2%) 1 (1%) 28 (28%) 0 (0%) Hemangioma 30 0 (0%) 0 (0%) 45 (50%) 43 (48%) 0 (0%) 2 (2%) 0 (0%) 0 (0%)

Note. Numbers in parentheses are the percentage for the mean number of readers who rated the lesions for each pattern.

m-HCC, moderately differentiated hepatocellular carcinoma; p-HCC, poorly differentiated hepatocellular carcinoma; w-HCC, well-differentiated hepatocellular carcinoma.

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Table 3

Performance of CAD Scheme for Classification in Five Categories Using Physicians’ Subjective Pattern Classification

Classification with CAD HCC Lesion Number of Lesions w-HCC m-HCC p-HCC Metastasis Hemangioma HCC 74 w-HCC 23 15 (65.2%) 4 (17.4%) 4 (17.4%) 0 (0.0%) 0 (0.0%) m-HCC 36 16 (44.4%) 15 (41.7%) 5 (13.9%) 0 (0.0% 1 (2.7%) p-HCC 15 1 (6.7%) 1 (6.7%) 12 (80.0%) 1 (6.7%) 0 (0.0%) Metastasis 33 1 (3.0%) 0 (0.0%) 1 (3.0%) 28 (84.8%) 3 (9.1%) Hemangioma 30 0 (0.0%) 0 (0.0%) 1 (3.3%) 1 (3.3%) 28 (93.3%)

CAD, computed-aided diagnosis; m-HCC, moderately differentiated hepatocellular carcinoma; p-HCC, poorly differentiated hepatocellular carcinoma; w-HCC, well-differentiated hepatocellular carcinoma.

Overall diagnostic accuracy: 98/137 (71.5 %).

CAD performance was evaluated by a leave-one-case-out method.

Table 4

Performance of CAD Scheme for Classification in Three Categories Using Physicians’ Subjective Pattern Classification

Classification with CAD Lesion Number of Lesions HCC Metastasis Hemangioma HCC 74 73 (98.6%) 1 (1.4%) 0 (0.0%) Metastasis 33 2 (6.1%) 28 (84.8%) 3 (9.1%) Hemangioma 30 1 (3.3%) 1 (3.3%) 28 (93.3%)

CAD, computed-aided diagnosis; HCC, hepatocellular carcinoma.

Overall diagnostic accuracy: 129/137 (94.2 %).

CAD performance was evaluated by a leave-one-case out method.

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Figure 3, A 28-year-old man with alcoholic cirrhosis and hepatocellular carcinoma (arrows) . (a) Sagittal B-mode ultrasound shows hypoechoic mass (arrows) in right lobe of liver. (b) In arterial phase, lesion (arrows) shows diffuse homogeneous and slightly hypervascularity relative to liver parenchyma. Percutaneous biopsy revealed well-differentiated hepatocellular carcinoma.

Figure 4, A 73-year-old woman with hepatitis C cirrhosis and hepatocellular carcinoma (arrows) . (a) Oblique subcostal B-mode ultrasound shows mass (arrows) with thin hypoechoic rim in right lobe of liver. (b) In arterial phase, the lesion (arrows) shows diffuse homogeneous and fairly hypervascularity relative to liver parenchyma. Percutaneous biopsy revealed moderately differentiated hepatocellular carcinoma.

Figure 5, A 75-year-old man with hepatitis C cirrhosis and hepatocellular carcinoma (arrows) . (a) Oblique subcostal left-lobe B-mode ultrasound shows mosaic mass (arrows) . (b) In the arterial phase, lesion ( arrows ) shows diffuse heterogeneous and slightly hypovascularity relative to liver parenchyma. Percutaneous biopsy revealed poorly differentiated hepatocellular carcinoma.

Figure 6, A 38-year-old woman with liver hemangioma (arrows) . (a) Oblique subcostal B-mode ultrasound shows mass with hyperechoic rim (arrows) . (b) In the arterial phase, the image shows peripheral puddles of contrast that were enhanced more than the adjacent liver parenchyma.

Figure 7, A 65-year-old man with metastatic colon cancer (arrows) . (a) Intercostal B-mode ultrasound shows hypoechoic mass (arrows) . (b) In the arterial phase, lesion (arrows) shows marginal vascularity.

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Discussion

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Conclusion

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Acknowledgement

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