| Literature DB >> 21748625 |
Kazuki Takeishi1, Ken Shirabe, Takeo Toshima, Toru Ikegami, Kazutoyo Morita, Takasuke Fukuhara, Takashi Motomura, Yohei Mano, Hideaki Uchiyama, Yuji Soejima, Akinobu Taketomi, Yoshihiko Maehara.
Abstract
Interferon (IFN), which is the only possible agent for recurrent hepatitis C after liver transplantation, may cause serious immune-related disorders. We report a case of de novo autoimmune hepatitis (AIH), which developed subsequent to switching from 2b pegylated interferon-α (peg-IFN) to 2a peg-IFN after living donor liver transplantation (LDLT). A 51-year-old man with hepatitis C-associated liver cirrhosis underwent LDLT. About 13 months after the initiation of antiviral therapy, in the form of type 2b peg-IFN with ribavirin, a negative serum hepatitis C virus (HCV)-RNA titer was confirmed. Thereafter, the 2b peg-IFN was switched to 2a peg-IFN, 3 months after which severe liver dysfunction developed, despite a constantly negative HCV-RNA. Liver biopsy showed portal and periportal inflammatory infiltrates including numerous plasma cells, indicating AIH. He was treated with steroid pulse treatment, followed by high-level immunosuppression maintenance, but eventually died of Pneumocystis pneumonitis 4 months after the diagnosis of de novo AIH.Entities:
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Year: 2011 PMID: 21748625 DOI: 10.1007/s00595-010-4392-z
Source DB: PubMed Journal: Surg Today ISSN: 0941-1291 Impact factor: 2.549