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网格蛋白重链染色在小肝细胞癌诊断标志物组合中的诊断准确性。

Diagnostic accuracy of clathrin heavy chain staining in a marker panel for the diagnosis of small hepatocellular carcinoma.

机构信息

Department of Pathology, Istituto di Ricovero e Cura a Carattere Scientifico, Rozzano, Milan, Italy.

出版信息

Hepatology. 2011 May;53(5):1549-57. doi: 10.1002/hep.24218.

Abstract

UNLABELLED

The American Association for the Study of Liver Diseases guidelines recommend the use of all available markers for improving the accuracy of the diagnosis of small hepatocellular carcinoma (HCC). To determine whether clathrin heavy chain (CHC), a novel HCC marker, is effective in combination with glypican 3 (GPC3), heat shock protein 70, and glutamine synthetase, we compared the performances of a three-marker panel (without CHC) and a four-marker panel (with CHC) in a series of small HCCs (≤2 cm) and nonsmall HCCs by core biopsy with a 20- to 21-gauge needle. The series included 39 nonsmall HCCs and 47 small HCCs (86 in all); the latter showed a well-differentiated histology [small grade 1 (G1)] in 30 cases (63.8%). The panel specificity was analyzed with the adjacent/extranodular cirrhotic liver (n = 30) and low-grade (n = 15) and high-grade dysplastic nodules (n = 16) as a control group. Absolute specificity (100%) for HCC was obtained only when at least two of the markers were positive (which two markers were positive did not matter). The addition of CHC to the panel increased the diagnostic accuracy for small HCCs (from 76.9% to 84.3%), and there was an important gain in sensitivity (from 46.8% to 63.8%). The four-marker panel had lower rates of accuracy (67.4%) and sensitivity (50%) for small G1 HCCs versus nonsmall G1 HCCs (93.9% and 88.2%, respectively). In seven cases (including six small G1 HCCs), there was no staining with any of the markers. Cirrhotic control livers were stained for CHC in four cases (13.3%) and for GPC3 in one case (3.3%).

CONCLUSION

The addition of CHC to the panel supports the diagnosis of small HCCs in challenging nodules on thin core biopsy samples. Small G1 HCCs include a group of earlier tumors characterized by a more silent phenotype and the progressive acquisition of the markers under study. The search for additional markers for early HCC diagnosis is warranted.

摘要

未加说明

美国肝病研究学会指南建议使用所有可用的标志物来提高小肝细胞癌 (HCC) 诊断的准确性。为了确定新型 HCC 标志物网格蛋白重链 (CHC) 是否与磷脂酰基醇蛋白 3 (GPC3)、热休克蛋白 70 和谷氨酰胺合成酶联合使用有效,我们通过 20-21 号针芯的核心活检比较了无 CHC 的三标志物组合和有 CHC 的四标志物组合在一系列小 HCC(≤2cm)和非小 HCC 中的表现。该系列包括 39 个非小 HCC 和 47 个小 HCC(共 86 个);后者在 30 例(63.8%)中显示出良好分化的组织学[小 G1(G1)]。用相邻/节外肝硬化肝(n=30)和低级别(n=15)和高级别发育不良结节(n=16)作为对照组分析了组合的特异性。只有当至少有两种标志物为阳性时(哪种标志物为阳性并不重要),才能获得 HCC 的绝对特异性(100%)。将 CHC 添加到组合中提高了小 HCC 的诊断准确性(从 76.9%提高到 84.3%),并且灵敏度有了重要提高(从 46.8%提高到 63.8%)。对于小 G1 HCC 与非小 G1 HCC 相比,四标志物组合的准确性(分别为 67.4%和 93.9%)和灵敏度(分别为 50%和 88.2%)较低。在 7 例(包括 6 例小 G1 HCC)中,没有任何标志物染色。在 4 例(13.3%)肝硬化对照肝中发现 CHC 染色,在 1 例(3.3%)中发现 GPC3 染色。

结论

在薄芯活检样本中具有挑战性的结节中,将 CHC 添加到组合中支持小 HCC 的诊断。小 G1 HCC 包括一组早期肿瘤,其特征为更沉默的表型和研究中标志物的逐渐获得。值得寻找其他用于早期 HCC 诊断的标志物。

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