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A case of cholestatic autoimmune hepatitis and acute liver failure: an unusual hepatic manifestation of mixed connective tissue disease and Sjögrens syndrome.

机译:胆汁淤积性自身免疫性肝炎和急性肝功能衰竭的病例:混合性结缔组织病和干燥综合征的异常肝表现。

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摘要

Although hepatomegaly is reported to occur occasionally in patients with mixed connective tissue disease (MCTD) or Sjögren's syndrome (SS), autoimmune liver diseases such as primary biliary cirrhosis, sclerosing cholangitis, and autoimmune hepatitis in association with MCTD or SS have rarely been described. We report a case of severe cholestatic autoimmune hepatitis presenting with acute liver failure in a 40-yr-old female patient suffering from MCTD and SS. The diagnosis of MCTD and SS was made at the age of 38. The patient presented severe jaundice and elevation of conjugated bilirubin. The patient denied alcohol and drug use and had no evidence of viral hepatitis. On the 8th day of her hospitalization, the patient developed grade III hepatic encephalopathy. She was diagnosed as autoimmune hepatitis presenting with acute liver failure based on clinical features, positive FANA and anti-smooth muscle antibodies, negative anti-mitochondrial antibodies, high titers of serum globulin, liver biopsy findings, and a good response to corticosteroid therapy, The patient was managed with prednisolone and the clinical symptoms, liver function test results, and liver biopsy findings showed much improvement after steroid therapy.
机译:尽管据报道合并混合性结缔组织病(MCTD)或干燥综合征(SS)的患者偶尔会发生肝肿大,但很少描述与MCTD或SS相关的自身免疫性肝病,例如原发性胆汁性肝硬化,硬化性胆管炎和自身免疫性肝炎。我们报道了一名患有MCTD和SS的40岁女性患者的严重胆汁淤积性自身免疫性肝炎,并伴有急性肝衰竭。 MCTD和SS的诊断在38岁时进行。患者出现严重的黄疸和结合胆红素升高。该患者否认饮酒和吸毒,也没有病毒性肝炎的证据。在住院的第8天,患者发展为III级肝性脑病。根据临床特征,FANA和抗平滑肌抗体阳性,抗线粒体抗体阴性,血清球蛋白高滴度,肝活检结果以及对皮质类固醇疗法的良好反应,她被诊断为患有急性肝衰竭的自身免疫性肝炎。该患者接受泼尼松龙治疗,类固醇治疗后临床症状,肝功能检查结果和肝活检结果均明显改善。

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