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Immunohistochemical panel of glypican-3, hepatocyte paraffin antigen-1, arginase-1, cytokeratin-19, and human epithelial membrane antigen for the differential diagnosis of liver tumors 被引量:2

Immunohistochemical panel of glypican-3, hepatocyte paraffin antigen-1, arginase-1, cytokeratin-19, and human epithelial membrane antigen for the differential diagnosis of liver tumors
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摘要 Objective Clinical immunohistochemistry plays an increasingly important role in pathologic diagnosis. We investigated the usefulness of an immunohistochemical panel of glypican-3 (GPC3), hepatocyte paraffin antigen-1 (HepPar-1), arginase-1 (Arg-1), cytokeratin-19 (CK19), and human epithelial membrane antigen (EMA) for the differential diagnosis of liver tumors. Methods Two hundred and thirty-five immunohistochemical sections of hepatocellular carcinoma (HCC;120 cases), intrahepatic cholangiocarcinoma (ICC;50 cases), combined hepatocellular and cholangiocarcinoma (CHC;17 cases), metastatic adenocarcinoma (20 cases), and benign liver lesions (28 cases) were obtained from the Department of Pathology at Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. The sensitivity and specificity of the combined biomarkers GPC3/HepPar-1/Arg-1/CK19/EMA for the differential diagnosis of HCC, ICC, and CHC were calculated and analyzed retrospectively. Results The combined biomarkers GPC3+/CK19– had the highest specificity (98.3%) for diagnosing HCC, with a sensitivity of 60.0%. The specificity of GPC3–/HepPar-1–/Arg-1–/CK19+/EMA+ for diagnosing ICC was 93.0%, with a sensitivity of 76.0%. The specificity of GPC3+/HepPar-1+/Arg-1+/CK19+/EMA+ for diagnosing CHC was 95.9%, with a sensitivity of 52.9%. Conclusion The combined biomarkers GPC3/HepPar-1/Arg-1/CK19/EMA greatly improved the specificity of liver tumor diagnosis. We believe that clinical pathological work could improve the original determination of liver nodules. Objective Clinical immunohistochemistry plays an increasingly important role in pathologic diagnosis. We investigated the usefulness of an immunohistochemical panel of glypican-3(GPC3), hepatocyte paraffin antigen-1(Hep Par-1), arginase-1(Arg-1), cytokeratin-19(CK19), and human epithelial membrane antigen(EMA) for the differential diagnosis of liver tumors. Methods Two hundred and thirty-five immunohistochemical sections of hepatocellular carcinoma(HCC; 120 cases), intrahepatic cholangiocarcinoma(ICC; 50 cases), combined hepatocellular and cholangiocarcinoma(CHC; 17 cases), metastatic adenocarcinoma(20 cases), and benign liver lesions(28 cases) were obtained from the Department of Pathology at Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China. The sensitivity and specificity of the combined biomarkers GPC3/Hep Par-1/Arg-1/CK19/EMA for the differential diagnosis of HCC, ICC, and CHC were calculated and analyzed retrospectively. Results The combined biomarkers GPC3+/CK19– had the highest specificity(98.3%) for diagnosing HCC, with a sensitivity of 60.0%. The specificity of GPC3–/Hep Par-1–/Arg-1–/CK19+/EMA+ for diagnosing ICC was 93.0%, with a sensitivity of 76.0%. The specificity of GPC3+/Hep Par-1+/Arg-1+/CK19+/EMA+ for diagnosing CHC was 95.9%, with a sensitivity of 52.9%.Conclusion The combined biomarkers GPC3/Hep Par-1/Arg-1/CK19/EMA greatly improved the specificity of liver tumor diagnosis. We believe that clinical pathological work could improve the original determination of liver nodules.
出处 《Oncology and Translational Medicine》 2019年第4期153-161,共9页 肿瘤学与转化医学(英文版)
基金 Supported by grants from National Natural Science Foundation of China(NSFC No.81271600,81671718 and 81873903) the Natural Science Foundation of Hubei Province in China(No.2016CFB687) the Clinical Foundation of Tongji Hospital(No.2015C013)
关键词 HEPATOCELLULAR carcinoma (HCC) INTRAHEPATIC CHOLANGIOCARCINOMA (ICC) combined HEPATOCELLULAR and CHOLANGIOCARCINOMA (CHC) immunohistochemistry hepatocellular carcinoma (HCC) intrahepatic cholangiocarcinoma (ICC) combined hepatocellular and cholangiocarcinoma(CHC) immunohistochemistry
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