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首页> 外文期刊>World journal of gastroenterology : >Autoimmune hepatitis-primary biliary cirrhosis concurrent with biliary stricture after liver transplantation
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Autoimmune hepatitis-primary biliary cirrhosis concurrent with biliary stricture after liver transplantation

机译:肝移植后自身免疫性肝炎原发性胆汁性肝硬化并发胆道狭窄

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摘要

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 anti-mitochondrial 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.
机译:尽管已在儿童和成人中描述了肝移植(LT)后从头发生的自身免疫性肝病的发展,但在肝移植接受者中很少见到自身免疫性肝炎(AIH)-原发性胆汁性肝硬化(PBC)重叠综合征。在此,我们报道了一名50岁的男性,该男性因酒精性脂肪性肝炎继发的代偿性肝病而接受LT。 LT后8年,他的肝功能检查明显异常。标准的自身免疫血清学测试显示抗核和抗线粒体抗体呈阳性,并且观察到对由泼尼松和熊去氧胆酸组成的方案添加显着生化反应,以维持他克莫司的免疫抑制作用。肝活检显示中度胆管病变和门静脉淋巴细胞浸润并伴有轻度纤维化,证实了AIH-PBC重叠综合征的诊断。我们认为这可能是LT后新发AIH-PBC重叠综合征的病例。一种新型的自身免疫重叠综合征。

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