"From Cholestasis to Interface Hepatitis: A Rare Case of Primary Sclerosing Cholangitis-Autoimmune Hepatitis Overlap in a 20-Year-Old Male".

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL
Clinical Medicine Insights. Case Reports Pub Date : 2026-08-07 eCollection Date: 2026-01-01 DOI:10.1177/11795476261470617
M Hassaan Shah, Aeman Daud Sethi, Muhammad Osama, Samar Hasnain, Rahat Shah, Irfan Khan, Aamir Khan, Pawan Kumar Thada
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Abstract

Introduction: Overlap syndrome refers to the coexistence of more than one immune-mediated liver disease in a single patient. Primary sclerosing cholangitis-autoimmune hepatitis (PSC-AIH) overlap is a rare but clinically important entity, as delayed recognition may lead to progressive liver injury, cirrhosis, and liver failure. Differentiating this condition from isolated PSC or AIH remains challenging due to overlapping clinical, biochemical, and radiological features.

Case presentation: A 20-year-old male presented with progressive jaundice, pruritus, acholic stools, and dark urine for one month. Laboratory evaluation revealed marked cholestasis with significantly elevated alkaline phosphatase and transaminases, hyperbilirubinemia, and coagulopathy, while viral and metabolic causes were excluded. Magnetic resonance cholangiopancreatography demonstrated characteristic intrahepatic biliary duct irregularities consistent with primary sclerosing cholangitis. However, disproportionately elevated alanine aminotransferase and serum immunoglobulin G levels prompted further evaluation. Liver biopsy revealed features of both diseases, including interface hepatitis with chronic portal inflammation and plasma cell infiltration, along with bile duct injury, ductopenia, and onion-skin fibrosis. Based on histology and diagnostic scoring, a diagnosis of PSC-AIH overlap syndrome was established. The patient was treated with ursodeoxycholic acid, corticosteroids, and azathioprine, resulting in marked clinical and biochemical improvement on follow-up.

Conclusion: This case highlights the importance of considering PSC-AIH overlap syndrome in young patients with cholestatic liver disease and unexpectedly elevated transaminases or immunoglobulin G levels. Early recognition and combined immunosuppressive and supportive therapy can lead to favorable outcomes and may prevent irreversible liver damage.

从胆汁淤积到界面肝炎:一例20岁男性原发性硬化性胆管炎-自身免疫性肝炎重叠病例。
简介:重叠综合征是指同一患者同时存在一种以上的免疫介导性肝病。原发性硬化性胆管炎-自身免疫性肝炎(PSC-AIH)重叠是一种罕见但临床上重要的实体,因为延迟识别可能导致进行性肝损伤,肝硬化和肝功能衰竭。由于临床、生化和放射学特征重叠,将这种情况与孤立的PSC或AIH区分仍然具有挑战性。病例介绍:一名20岁男性,以进行性黄疸、瘙痒、胆汁性便、尿色深一个月为临床表现。实验室评估显示明显的胆汁淤积,碱性磷酸酶和转氨酶显著升高,高胆红素血症和凝血功能障碍,而病毒和代谢原因被排除在外。磁共振胆管造影显示特征性肝内胆管不规则,符合原发性硬化性胆管炎。然而,不成比例地升高的丙氨酸转氨酶和血清免疫球蛋白G水平促使进一步的评估。肝活检显示两种疾病的特征,包括界面肝炎合并慢性门静脉炎和浆细胞浸润,同时伴有胆管损伤、胆管减少和洋葱皮纤维化。根据组织学和诊断评分,确定PSC-AIH重叠综合征的诊断。患者给予熊去氧胆酸、皮质类固醇和硫唑嘌呤治疗,随访时临床和生化均有明显改善。结论:本病例强调了考虑PSC-AIH重叠综合征在年轻胆汁淤积性肝病患者和转氨酶或免疫球蛋白G水平意外升高的重要性。早期识别和联合免疫抑制和支持治疗可导致良好的结果,并可能防止不可逆的肝损伤。
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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来源期刊
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights. Case Reports MEDICINE, GENERAL & INTERNAL-
CiteScore
1.10
自引率
0.00%
发文量
57
审稿时长
8 weeks
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