| Literature DB >> 28970136 |
Ian Clark1, Sejal S Shah2, Roger Moreira2, Rondell P Graham2, Tsung-Teh Wu2, Michael S Torbenson2, Vishal Chandan3.
Abstract
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.Entities:
Keywords: Arginase-1; Hepatocellular carcinoma; Liver; Well differentiated
Mesh:
Substances:
Year: 2017 PMID: 28970136 DOI: 10.1016/j.humpath.2017.09.007
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466