| Literature DB >> 27900094 |
Tomohiro Iguchi1, Motoyuki Yamagata2, Takashi Sonoda2, Kimihiko Yanagita3, Tetsuhiro Fukahori4, Eiji Tsujita1, Shinichi Aishima5, Yoshinao Oda6, Yoshihiko Maehara7.
Abstract
Malignant transformation of hepatocellular adenoma (HA) is relatively rare and has been reported to be associated with dysregulation of the β-catenin pathway. The presence of bone marrow metaplasia in HA is an uncommon histological characteristic. The current report presents the case of a 46-year-old woman with glycogen storage disease type I (von Gierke's disease) who underwent resection of hepatocellular carcinoma (HCC) arising in a HA with associated bone marrow metaplasia producing three series of hematopoietic cells. The serum level of proteins induced by des-gamma-carboxy prothrombin (DCP) gradually increased as the tumors grew; following hepatic resection, DCP levels returned to normal. Nuclear accumulation of β-catenin was shown in HCC by immunohistochemistry; however, no mutation was detected in exon 3 of β-catenin. To the best of our knowledge, this is the first report of HA with absolute bone marrow metaplasia producing three series of hematopoietic cells. This occurrence suggests that elevated DCP may be an indicator of malignant transformation of HA.Entities:
Keywords: bone marrow metaplasia; des-gamma-carboxy prothrombin; hepatocellular adenoma; hepatocellular carcinoma; β-catenin
Year: 2016 PMID: 27900094 PMCID: PMC5103882 DOI: 10.3892/mco.2016.1034
Source DB: PubMed Journal: Mol Clin Oncol ISSN: 2049-9450