| Literature DB >> 15075999 |
Tetsuhiro Chiba1, Shigemasa Goto, Osamu Yokosuka, Fumio Imazeki, Masamichi Tanaka, Kenichi Fukai, Yoko Takahashi, Hideki Tsujimura, Hiromitsu Saisho.
Abstract
We report a 22-year-old female who presented with pyrexia, pancytopenia and liver dysfunction. The patient showed mild liver dysfunction with low-grade fever and mild hepatosplenomegaly 6 years previously, and autoimmune hepatitis (AIH) was diagnosed based on the examination of the laboratory data and liver biopsy. On admission, both markers of Epstein-Barr virus (EBV) and in-situ hybridisation from a liver biopsy specimen indicated chronic active EBV infection (CAEBV). The patient was administered an immunosuppressive agent and antiviral drug added to steroid therapy, but ultimately died from liver failure and virus-associated haemophagocytosis 10 months after the definite diagnosis. Retrospective examination of the serum at the diagnosis of AIH revealed extremely high titres of antibody to EBV, and EBV-DNA was also detectable by polymerase chain reaction. These results suggest the possibility that the patient may already have suffered from CAEBV at the initial diagnosis. We presume that hepatic involvement of CAEBV should be considered as differential diagnosis in cases showing liver dysfunction with clinical and biochemical features observed in AIH.Entities:
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Year: 2004 PMID: 15075999 DOI: 10.1097/00042737-200402000-00017
Source DB: PubMed Journal: Eur J Gastroenterol Hepatol ISSN: 0954-691X Impact factor: 2.566