| Literature DB >> 18414167 |
Joseph S Chan1, Cary O Harding, Charles D Blanke.
Abstract
A young patient with hepatocellular carcinoma receiving chemotherapy presented with encephalopathy. Evaluation of the patient revealed a metabolic profile consistent with ornithine transcarbamoylase (OTC) deficiency, an inherited disorder of the urea cycle. The evaluation yielded a plasma amino acid analysis consistent with OTC deficiency. However, genetic analysis did not reveal a somatic mutation of the OTC gene in this patient. The hyperammonemic encephalopathy was reversed by the infusion of arginine, a common treatment for hereditary OTC deficiency. This case may represent a distinct syndrome of reversible hyperammonemia in patients with hepatocellular carcinoma.Entities:
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Year: 2008 PMID: 18414167 DOI: 10.1097/SMJ.0b013e31816bf5cc
Source DB: PubMed Journal: South Med J ISSN: 0038-4348 Impact factor: 0.954