Patedakis Litvinov Bogdan Ioannis, Pathak Amit P
Department of Medicine, Georgetown University School of Medicine, Washington, DC, USA.
Department of Internal Medicine, MedStar Washington Hospital Center, Washington, DC, USA.
BMJ Case Rep. 2017 Sep 7;2017:bcr-2017-220988. doi: 10.1136/bcr-2017-220988.
We describe a case of a 23-year-old woman with a history of Crohn's disease (CD), who initially presented with sepsis-like symptoms, subsequently developed severe cholestasis and following extensive inpatient workup was found to have non-caseating granulomas on her liver biopsy. Infectious aetiologies were excluded and the patient was treated with oral corticosteroids, which ameliorated but did not completely reverse the cholestasis. We review the differential diagnosis of hepatic granulomas and discuss the potential difficulties in establishing their exact aetiology in patients with CD.
我们描述了一例23岁患有克罗恩病(CD)的女性病例,该患者最初表现出类似败血症的症状,随后发展为严重胆汁淤积,经过广泛的住院检查,肝脏活检发现有非干酪样肉芽肿。排除了感染性病因,患者接受口服皮质类固醇治疗,胆汁淤积有所改善但未完全逆转。我们回顾了肝肉芽肿的鉴别诊断,并讨论了在CD患者中确定其确切病因的潜在困难。