Hui Monalisa, Uppin Shantveer G, Uppin Megha S, Madhav T Venu, Varma G Surya Ramachandra, Paul Tara Roshni, Bheerappa N
Department of Pathology, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana, India.
Department of Surgical Gastroenterology, Nizam's Institute of Medical Sciences, Punjagutta, Hyderabad, Telangana, India.
Indian J Cancer. 2023 Apr-Jun;60(2):191-198. doi: 10.4103/ijc.IJC_1004_19.
Diagnosis of hepatocellular carcinoma (HCC) is difficult on morphology alone in poorly differentiated tumors and metastatic carcinomas. Appropriate immunohistochemical markers are required for definite diagnosis. In this article, we have analyzed the histopathological and immunohistochemical features of HCC and elucidate the best possible immunohistochemistry (IHC) marker combination by comparing the sensitivity of various markers in different grades of tumor.
A total of 116 consecutive cases were analyzed retrospectively. The hematoxylin and eosin stained sections were reviewed in all the cases. IHC was done using hepatocellular specific antigen (HSA), arginase-1, glypican-3, and polyclonal carcinoembryonic antigen (pCEA). The sensitivity of various immunohistochemical markers individually as well as in combination for different tumor grades was determined.
Histologically, the predominant subtype comprised of classic variant (109,93.9%) followed by combined hepatocellular and cholangiocarcinoma (4,3.4%) and fibrolamellar variant (3,2.6%). Trabecular pattern was the most common histological pattern. On grading, 65,56.03% were moderately differentiated, 34,29.31% well differentiated, and17, 14.65% poorly differentiated. HSA and polyclonal-CEA showed higher sensitivity than arginase-1 and glypican-3 in well and moderately differentiated tumors. In contrast arginase-1 and glypican-3 showed better sensitivity in poorly differentiated HCC. The overall sensitivity increased to greater than 90% if HSA/polyclonal-CEA is combined with either arginase-1/glypican-3 irrespective of tumor grade.
Majority of the tumors were classic variants and moderately differentiated. HSA along with either arginase-1 or glypican-3 is the best combination of immunomarker for identification of hepatocellular differentiation irrespective of tumor grade.
对于低分化肿瘤和转移性癌,仅依靠形态学诊断肝细胞癌(HCC)存在困难。明确诊断需要合适的免疫组化标志物。在本文中,我们分析了HCC的组织病理学和免疫组化特征,并通过比较不同级别肿瘤中各种标志物的敏感性,阐明了最佳的免疫组化(IHC)标志物组合。
回顾性分析了116例连续病例。对所有病例的苏木精-伊红染色切片进行复查。使用肝细胞特异性抗原(HSA)、精氨酸酶-1、磷脂酰肌醇蛋白聚糖-3和多克隆癌胚抗原(pCEA)进行免疫组化检测。确定了不同肿瘤级别中各种免疫组化标志物单独及联合使用时的敏感性。
组织学上,主要亚型为经典型(109例,93.9%),其次为肝细胞胆管癌混合型(4例,3.4%)和纤维板层型(3例,2.6%)。小梁状模式是最常见的组织学模式。分级方面,65例(56.03%)为中分化,34例(29.31%)为高分化,17例(14.65%)为低分化。在高分化和中分化肿瘤中,HSA和多克隆CEA的敏感性高于精氨酸酶-1和磷脂酰肌醇蛋白聚糖-3。相反,精氨酸酶-1和磷脂酰肌醇蛋白聚糖-3在低分化HCC中显示出更好的敏感性。无论肿瘤级别如何,若将HSA/多克隆CEA与精氨酸酶-1/磷脂酰肌醇蛋白聚糖-3联合使用,总体敏感性可提高到90%以上。
大多数肿瘤为经典型且为中分化。无论肿瘤级别如何,HSA与精氨酸酶-1或磷脂酰肌醇蛋白聚糖-3联合是识别肝细胞分化的最佳免疫标志物组合。