Comparing the computed tomography radiologic features of cytokeratin 19-positive hepatocellular carcinoma to those of conventional hepatocellular carcinoma and intrahepatic cholangiocarcinoma

比较细胞角蛋白19阳性肝细胞癌与传统肝细胞癌和肝内胆管癌的计算机断层扫描放射学特征

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Abstract

BACKGROUND: Cytokeratin 19-positive hepatocellular carcinoma (CK19(+) HCC) is an uncommon subtype of hepatocellular carcinoma (HCC). The purpose of this study was to identify radiological characteristics with diagnostic value for CK19(+) HCC. METHODS: This was a case-control study. A retrospective analysis of 104 patients with surgically resected, pathologically confirmed CK19(+) HCC was conducted. The contrast-enhanced computed tomography characteristics of the enrolled patients were assessed, and differences in characteristics between groups were identified by statistical analysis. A multivariate logistic regression model was established to identify CK19(+) HCC, and receiver operating characteristic curves were plotted to evaluate the diagnostic performance of the model. RESULTS: The univariate analysis revealed that the frequency of regular morphology (55.8% vs. 35.6%, P<0.001), hypodensity (99.0% vs. 91.8%, P=0.010), intratumoral necrosis (61.5% vs. 25.0%, P<0.001), heterogeneous enhancement (96.2% vs. 86.5%, P=0.008), peripheral washout (5.8% vs. 1.4%, P=0.031), non-peripheral washout (88.5% vs. 45.7%, P<0.001), Liver Imaging Reporting and Data System category 5 (67.3% vs. 40.4%, P<0.001), and Liver Imaging Reporting and Data System - Category tumor in vein (LR-TIV) (16.3% vs. 2.4%, P<0.001) were significantly higher in CK19(+) HCC than the non-CK19+ hepatic tumor patients. Conversely, the incidence of rim enhancement in the arterial phase (7.7% vs. 22.6%, P=0.001), transient hepatic attenuation difference (THAD; 4.8% vs. 23.1%, P<0.001), pseudocapsule formation (12.5% vs. 23.6%, P=0.021), progressive enhancement (5.8% vs. 50.5%, P<0.001), and lymphadenopathy (9.6% vs. 24.5%, P=0.002) was significantly lower in the CK19(+) HCC than the non-CK19(+) hepatic tumor patients. The multivariate analysis identified intratumoral necrosis, THAD, pseudocapsule formation, progressive enhancement, and LR-TIV as independent predictors of CK19+ HCC (P<0.05). The joint prediction model had an area under the curve of 0.867 in terms of its ability to detect CK19(+) HCC, and a sensitivity of 88.46% and a specificity of 69.71%. CONCLUSIONS: CK19(+) HCC is characterized by an increased prevalence of intratumoral necrosis and LR-TIV, as well as a lower incidence of THAD, pseudocapsule formation, and progressive enhancement, which collectively contribute to the identification of this HCC variant.

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