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原发性胆汁性胆管炎合并CREST综合征时的非肝硬化门静脉高压症。

Noncirrhotic portal hypertension in primary biliary cholangitis with coexisting CREST syndrome.

作者信息

Malkani Kabir V, Jesudian Arun B, Luo Jean J, Schonfeld Emily A

机构信息

Division of Gastroenterology and Hepatology, Weill Cornell Medical College, New York, NY, USA.

Division of Gastroenterology and Hepatology, Weill Cornell Medical College, New York, NY, USA.

出版信息

Clin Res Hepatol Gastroenterol. 2023 May;47(5):102114. doi: 10.1016/j.clinre.2023.102114. Epub 2023 Mar 24.

Abstract

Primary Biliary Cholangitis (PBC) is an autoimmune liver disease that is sometimes associated with CREST (calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia) syndrome. If left untreated, PBC eventually progresses to liver cirrhosis. We describe an adult patient with CREST-PBC who presented with recurrent variceal bleeding and ultimately required transjugular intrahepatic portosystemic shunt (TIPS) insertion. Liver biopsy excluded cirrhosis, resulting in a diagnosis of noncirrhotic portal hypertension. This case report describes the pathophysiology of presinusoidal portal hypertension as a rare complication of PBC and its association with coexisiting CREST.

摘要

原发性胆汁性胆管炎(PBC)是一种自身免疫性肝病,有时与CREST(钙质沉着、雷诺现象、食管动力障碍、指(趾)硬皮病和毛细血管扩张)综合征相关。如果不进行治疗,PBC最终会发展为肝硬化。我们描述了一名患有CREST-PBC的成年患者,该患者反复出现静脉曲张出血,最终需要行经颈静脉肝内门体分流术(TIPS)。肝活检排除了肝硬化,诊断为非肝硬化性门静脉高压症。本病例报告描述了肝前性门静脉高压作为PBC罕见并发症的病理生理学及其与并存的CREST的关联。

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