Autoimmune hepatitis-primary biliary cirrhosis concurrent with biliary stricture after liver transplantation

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Abstract

Although the development of de novo autoimmune liver disease after liver transplantation (LT) has been described in both children and adults, autoimmune hepatitis (AIH)-primary biliary cirrhosis (PBC) overlap syndrome has rarely been seen in liver transplant recipients. Here, we report a 50-year-old man who underwent LT for decompensated liver disease secondary to alcoholic steatohepatitis. His liver function tests became markedly abnormal 8 years after LT. Standard autoimmune serological tests were positive for anti-nuclear and antimitochondrial antibodies, and a marked biochemical response was observed to a regimen consisting of prednisone and ursodeoxycholic acid added to maintain immunosuppressant tacrolimus. Liver biopsy showed moderate bile duct lesions and periportal lymphocytes infiltrating along with light fibrosis, which confirmed the diagnosis of AIH-PBC overlap syndrome. We believe that this may be a case of post-LT de novo AIH-PBC overlap syndrome; a novel type of autoimmune overlap syndrome.

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APA

Kang, Y. Z., Sun, X. Y., Liu, Y. H., & Shen, Z. Y. (2015). Autoimmune hepatitis-primary biliary cirrhosis concurrent with biliary stricture after liver transplantation. World Journal of Gastroenterology, 21(7), 2236–2241. https://doi.org/10.3748/wjg.v21.i7.2236

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