肉样瘤病与原发性胆汁性肝硬化的关联:新发现

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摘要

肉样瘤病是一种病因不明的全身性疾病。其特征是受累器官出现非溃疡性肉芽肿病变。原发性胆汁性肝硬化(PBC)是一种慢性自身免疫性胆汁淤积性肝病,其特点是胆管被破坏和存在 M2 型抗线粒体抗体 [1]。这里报告的肉样瘤病与原发性胆汁性肝硬化的关联是罕见的。这给组织学鉴别诊断带来了难题,并提出了这两种疾病之间存在病因联系的假设[2]。我们报告了一名在卡萨布兰卡chu ibno rochd医院内科住院的患者的临床病例,该患者被诊断为肉样瘤病和原发性胆汁性肝硬化并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of Sarcoidosis and Primary Biliary Cirrhosis: A New Observation
Sarcoidosis is a systemic disease of unknown etiology. It is characterized by the presence of noncaseating granulomatous lesions in the affected organs. Primary biliary cirrhosis (PBC) is a chronic autoimmune cholestatic hepatopathy characterized by destruction of the bile ducts and the presence of M2-type anti-mitochondrial antibodies [1]. The association of sarcoidosis and primary biliary cirrhosis reported here is rare. It poses a problem of histological differential diagnosis and raises the hypothesis of an etiopathogenic link between the two conditions [2]. We report the clinical case of a patient hospitalized in the internal medicine department of chu ibno rochd casablanca, who was diagnosed with a combination of sarcoidosis and primary biliary cirrhosis.
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