特发性成年ductopia的晚期表现。

C Müller, W Ulrich, E Penner
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引用次数: 14

摘要

特发性成人胆管减少症是一种病因不明的慢性胆汁淤积性肝病,以小叶间胆管丧失为特征。我们描述了3例符合特发性成人胆管减少症诊断标准的患者,但与迄今为止报道的病例不同,在疾病的晚期表现和良性临床过程中,尽管组织学证据表明胆管炎持续存在。1例患者接受熊去氧胆酸治疗后,胆汁淤积的生化指标有所改善,提示特发性成人胆管减少症的慢性胆汁淤积可以得到有益的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Manifestation late in life of idiopathic adulthood ductopenia.

Idiopathic adulthood ductopenia is a chronic cholestasic liver disease of unknown etiology characterized by the loss of interlobular bile ducts. We describe three patients who fulfilled the diagnostic criteria of idiopathic adulthood ductopenia, but differed from the cases reported so far in late manifestation of the disease and a benign clinical course despite histologic evidence of ongoing cholangitis. Treatment with ursodeoxycholic acid in one patient resulted in improvement of biochemical markers of cholestasis, suggesting that chronic cholestasis in idiopathic adulthood ductopenia can be influenced beneficially.

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