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1例类风湿关节炎先于原发性胆汁性肝硬化且抗线粒体抗体阴性的病例

[A case of primary biliary cirrhosis with negative anti-mitochondrial antibody anteceded by rheumatoid arthritis].

作者信息

Nakano T, Ishibashi H, Matsui M, Yasutake T, Ishii Y, Dohmen K, Nagasawa K, Niho Y

机构信息

First Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka.

出版信息

Fukuoka Igaku Zasshi. 1992 Mar;83(3):144-8.

PMID:1559653
Abstract

We report a case of primary biliary cirrhosis with negative anti-mitochondrial antibody which were anteceded by rheumatoid arthritis. The patient was a 46-year-old female who was admitted due to low grade fever and elevated serum alkaline phosphatase (ALP) and gamma-glutamyl transpeptidase (gamma-GTP) levels. She had been diagnosed as having erythema nodosum and rheumatoid arthritis 6 years before. Her family history disclosed that her mother had rheumatoid arthritis and her sister systemic lupus erythematosus. On admission, she had moderately elevated erythrocyte sedimentation rate, and elevated serum ALP, gamma-GTP and IgM levels. Anti-mitochondrial antibody and anti-pyruvate dehydrogenase complex antibody were negative but anti-nuclear antibody was positive. However, the histology of liver showed chronic non-suppurative destructive cholangitis. AMA was always negative and serum ALP and bilirubin levels remained constant during the following two years. The pathogenesis of primary biliary cirrhosis with negative anti-mitochondrial antibody is discussed.

摘要

我们报告一例原发性胆汁性肝硬化病例,该病例抗线粒体抗体阴性,之前患有类风湿关节炎。患者为一名46岁女性,因低热、血清碱性磷酸酶(ALP)和γ-谷氨酰转肽酶(γ-GTP)水平升高入院。她6年前被诊断为结节性红斑和类风湿关节炎。她的家族史显示,她的母亲患有类风湿关节炎,她的姐姐患有系统性红斑狼疮。入院时,她的红细胞沉降率中度升高,血清ALP、γ-GTP和IgM水平升高。抗线粒体抗体和抗丙酮酸脱氢酶复合物抗体均为阴性,但抗核抗体为阳性。然而,肝脏组织学显示为慢性非化脓性破坏性胆管炎。在接下来的两年里,AMA始终为阴性,血清ALP和胆红素水平保持稳定。本文讨论了抗线粒体抗体阴性的原发性胆汁性肝硬化的发病机制。

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