| Literature DB >> 27591041 |
Kohtaro Ooka1, Ifeyinwa Onyiuke2, Xuchen Zhang3, Tamar Hamosh Taddei4.
Abstract
Hereditary haemochromatosis is a multisystem disorder of iron metabolism. Hepatic manifestations include hepatomegaly, cirrhosis and hepatocellular carcinoma. Hepatocellular carcinoma is almost always preceded by cirrhosis. We present a case of an 83-year-old man without history of liver disease or iron overload who presented with abdominal pain. Workup revealed mildly elevated transaminases, ferritin of 3996 and a solitary liver tumour. Biopsy was consistent with hepatocellular carcinoma in a background of haemosiderosis without cirrhosis. He was diagnosed with hereditary haemochromatosis and hepatocellular carcinoma. He underwent a partial hepatectomy and was started on routine phlebotomy and surveillance imaging. He has improved and has not had signs of recurrence or new complications of haemochromatosis. We suggest a possible reason for his unique and late presentation. 2016 BMJ Publishing Group Ltd.Entities:
Mesh:
Year: 2016 PMID: 27591041 PMCID: PMC5020720 DOI: 10.1136/bcr-2016-216649
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X