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Combined hepatocellular‐cholangiocarcinoma in a patient with Abernethy malformation and tetralogy of Fallot: A case report
Author(s) -
Happaerts Sofie,
Foucault Amélie,
Billiard Jean Sébastien,
Nguyen Bich,
VandenbrouckeMenu Franck
Publication year - 2016
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1002/hep.28656
Subject(s) - medicine , nodular regenerative hyperplasia , tetralogy of fallot , hepatology , focal nodular hyperplasia , hepatocellular carcinoma , esophageal varices , congenital hepatic fibrosis , portal vein , cirrhosis , gastroenterology , pathology , portal hypertension , heart disease
Abernethy malformation is a rare congenital anomaly of the portal vein where the portal blood bypasses the liver. We report the first case of a patient with Abernethy malformation and tetralogy of Fallot associated with nodular regenerative hyperplasia and focal nodular hyperplasia (FNH), which finally evolved to a giant hepatocellular‐cholangiocarcinoma (HCC‐CC) of the liver, successfully resected. (H epatology 2016;64:1800‐1802)