A rare etiology of persistent jaundice in type 1 autoimmune hepatitis.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL Archive of clinical cases Pub Date : 2021-12-29 eCollection Date: 2021-01-01 DOI:10.22551/2021.32.0803.10183
Budumuri Gautam V Kumar, Purna Ch Sethy, Rohit Gupta
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Abstract

A 24-year-old male without previously known comorbidities presented with progressive jaundice and hepatomegaly. Autoimmune serology and liver biopsy revealed features of autoimmune hepatitis. A treatment by oral prednisolone and azathioprine was initiated, after which he achieved remission. However, hyperbilirubinemia persisted, with a predominantly unconjugated fraction. Hemolytic causes of unconjugated hyperbilirubinemia were ruled out, and the diagnosis of Gilbert syndrome was established.

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1型自身免疫性肝炎持续性黄疸的罕见病因。
24岁男性,既往无已知合并症,表现为进行性黄疸和肝肿大。自身免疫血清学和肝脏活检显示自身免疫性肝炎的特征。开始口服强的松龙和硫唑嘌呤治疗,之后患者获得缓解。然而,高胆红素血症持续存在,主要是未结合的部分。排除非结合性高胆红素血症的溶血性原因,并确定吉尔伯特综合征的诊断。
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