| Literature DB >> 28425418 |
Hui Li1, Zhi Ma1, Ying Xie1, Feng Tian1.
Abstract
The Abernethy malformation is a rare congenital malformation defined by the presence of an extrahepatic portosystemic shunt. Although most patients are asymptomatic, clinical encephalopathy is present in 15% of cases. We present a patient with type 2 Abernethy malformation, hyperammonemia, and encephalopathy. Shunt closure was performed successfully using interventional angiography; however, hyperammonemia recurred 3 months later. The diagnosis of Abernethy malformation can be made easily, but the ideal patient management strategy has not yet been established. This is the first reported patient with recurrence of hyperammonemia after interventional treatment; we discuss the therapeutic options for Abernethy malformation.Entities:
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Year: 2017 PMID: 28425418 DOI: 10.5604/16652681.1235492
Source DB: PubMed Journal: Ann Hepatol ISSN: 1665-2681 Impact factor: 2.400