[Two cases of autoimmnune hepatitis associated with systemic lupus erythematosus].

Jang Uk Yoon, Sang Hoon Park, Eun Jung Kim, Ji Hyun Hong, Hyung Seok Lee, Kil Chan Oh, Chul Hee Park, Tae Ho Hahn, Dong Keun Lee, Jong Hyeok Kim, Hae Lim Park, Choong Kee Park
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Abstract

Autoimmune hepatitis (AIH) is a chronic necroinflammatory liver disease of unknown cause associated with circulating autoantibodies and high serum globulin level. Systemic lupus erythematosus (SLE) is a disease of unknown etiology in which tissues and cells are damaged by pathogenic autoantibodies and immune complex, affecting multiple organs including the liver, kidney, and CNS. The difference between the hepatic involvement of SLE and autoimmune hepatitis has not been clearly defined in the past due to similarities in clinical and biochemical features. A scoring system for the diagnosis of AIH has been established, and AIH and SLE-associated hepatitis have been defined as two different entities, although both have the same autoimmune features such as polyarthralgia, hypergammaglobulinemia and circulating autoantibodies. AIH has been considered to occur infrequently in SLE. We report two cases of AIH which simultaneously satisfied the criteria of SLE.

自身免疫性肝炎合并系统性红斑狼疮2例
自身免疫性肝炎(AIH)是一种病因不明的慢性坏死性炎症性肝病,与循环自身抗体和高血清球蛋白水平有关。系统性红斑狼疮(SLE)是一种病因不明的疾病,其组织和细胞被致病性自身抗体和免疫复合物破坏,影响包括肝、肾和中枢神经系统在内的多个器官。由于在临床和生化特征上的相似性,SLE与自身免疫性肝炎累及肝脏的区别在过去一直没有明确界定。AIH的诊断评分系统已经建立,AIH和sleg相关性肝炎被定义为两种不同的实体,尽管两者具有相同的自身免疫特征,如多关节痛、高γ球蛋白血症和循环自身抗体。AIH被认为在SLE中很少发生。我们报告两例AIH同时满足SLE的标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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