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药物性狼疮样综合征伴严重自身免疫性肝炎。

Drug-induced lupus-like syndrome associated with severe autoimmune hepatitis.

作者信息

Graziadei I W, Obermoser G E, Sepp N T, Erhart K H, Vogel W

机构信息

Department of Gastroenterology and Hepatology, University of Innsbruck, Innsbruck, Austria.

出版信息

Lupus. 2003;12(5):409-12. doi: 10.1191/0961203303lu313cr.

Abstract

Atorvastatin and other members of the statin family are widely used for the treatment of hypercholesterolaemia in order to reduce the risk of atherosclerosis and cardiovascular disease. Atorvastatin-induced adverse events are mostly mild and only a few cases of lupus-like syndrome or severe acute hepatitis have been documented. In this case report we describe a patient who developed an atorvastatin-induced severe autoimmune hepatitis. In addition, this patient presented with a concomitant systemic lupus-like syndrome which has been already described for statins but not in association with severe liver disease. Although the drug was immediately withdrawn the disease persisted and even deteriorated to a fulminant disease with evidence of acute hepatic failure. The patient failed to respond to conventional immunosuppression with corticosteroids and azathioprine. Only the introduction of intense immunosuppressive therapy, as used in solid organ transplantation, led to a complete and sustained recovery of the patient. Interestingly, the patient was HLA DR3- and HLA DR4-positive, which are well-known genetic factors associated with autoimmune diseases. This case is the first report of a drug-induced lupus-likesyndrome concomitant with a severe autoimmune hepatitis in a genetically predisposed patient.

摘要

阿托伐他汀及他汀类家族的其他成员被广泛用于治疗高胆固醇血症,以降低动脉粥样硬化和心血管疾病的风险。阿托伐他汀引起的不良事件大多较为轻微,仅有少数狼疮样综合征或严重急性肝炎的病例被记录在案。在本病例报告中,我们描述了一名发生阿托伐他汀所致严重自身免疫性肝炎的患者。此外,该患者还伴有系统性狼疮样综合征,他汀类药物已有相关描述,但未与严重肝病相关联。尽管立即停用了该药物,但疾病仍持续存在,甚至恶化为暴发性疾病,并出现急性肝衰竭的迹象。该患者对使用皮质类固醇和硫唑嘌呤的传统免疫抑制治疗无反应。只有采用实体器官移植中使用的强化免疫抑制疗法,才使患者完全且持续康复。有趣的是,该患者为HLA DR3和HLA DR4阳性,这是与自身免疫性疾病相关的众所周知的遗传因素。本病例是首例关于在遗传易感性患者中药物诱导的狼疮样综合征合并严重自身免疫性肝炎的报告。

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