Clark Ian, Shah Sejal S, Moreira Roger, Graham Rondell P, Wu Tsung-Teh, Torbenson Michael S, Chandan Vishal
Department of Cellular Pathology, Royal Free Hospital, London, UK.
Division of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA.
Hum Pathol. 2017 Nov;69:90-95. doi: 10.1016/j.humpath.2017.09.007. Epub 2017 Sep 29.
Hepatocellular carcinoma (HCC) is a common malignancy both in the United States of America and worldwide. Despite the refinement of imaging techniques in at-risk populations, a needle biopsy diagnosis remains an important diagnostic tool for HCC in many cases. Various immunohistochemical markers have been developed to facilitate this diagnosis, such as HepPar-1, glypican-3 and, most recently, arginase-1. Amongst them, arginase-1 has been shown to have superior sensitivity and specificity than the others. Performance of arginase-1 has been reported to be excellent for diagnosis of well-differentiated HCCs, with some tail-off in sensitivity for poorly differentiated tumors. Our experience has suggested that a subset of well-differentiated HCCs can be negative for arginase-1. We examined 68 consecutive confirmed cases of well-differentiated HCC diagnosed on needle biopsy, and found 7 (10%) to be completely negative for arginase-1. This finding is of fundamental clinical importance in view of previous studies that have shown arginase-1 to be always positive in well-differentiated HCC.
肝细胞癌(HCC)在美国和全球都是一种常见的恶性肿瘤。尽管针对高危人群的成像技术有所改进,但在许多情况下,针吸活检诊断仍然是HCC的重要诊断工具。为了便于诊断,人们开发了各种免疫组化标志物,如HepPar-1、磷脂酰肌醇蛋白聚糖-3,以及最近的精氨酸酶-1。其中,精氨酸酶-1已被证明比其他标志物具有更高的敏感性和特异性。据报道,精氨酸酶-1在诊断高分化HCC方面表现出色,而对低分化肿瘤的敏感性则有所下降。我们的经验表明,一部分高分化HCC的精氨酸酶-1可能呈阴性。我们检查了68例经针吸活检确诊的连续高分化HCC病例,发现7例(10%)精氨酸酶-1完全阴性。鉴于之前的研究表明精氨酸酶-1在高分化HCC中总是呈阳性,这一发现具有重要的临床意义。