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Membranous glomerulonephritis associated with autoimmune hepatitis and primary biliary cirrhosis overlap syndrome: a very rare condition.

机译:与自身免疫性肝炎和原发性胆汁性肝硬化重叠综合征相关的膜性肾小球肾炎:一种非常罕见的疾病。

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摘要

Autoimmune hepatitis (AIH) and primary biliary cirrhosis (PBG) are typical autoimmune liver diseases that mainly affect middle-aged women. However, these disorders are not just limited to the liver and are often associated with various extrahepatic manifestations or other autoimmune diseases [ 1 ]. The term hepatic overlap syndrome is used to describe the coexistence of two autoimmune hepatic diseases, whereas AIH/PBG overlap syndrome is the most common form, affecting almost 10% of patients with AIH or PBG [2], Although the coexistence of AIH or PBG has been reported separately with a variety of other autoimmune diseases, there are limited reports of such association in a case of AIH/PBG overlap. Herein, we describe a case of AIH/PBG overlap associated with membranous glomerulonephritis (MGN), whose kidney and liver pathologies resolved after treatment of prednisolone, azathiopyr-ine (AZT) and ursodeoxycholic acid (UDCA).
机译:自身免疫性肝炎(AIH)和原发性胆汁性肝硬化(PBG)是典型的自身免疫性肝病,主要影响中年妇女。但是,这些疾病不仅限于肝脏,而且经常与各种肝外表现或其他自身免疫性疾病有关[1]。术语肝重叠综合征用于描述两种自身免疫性肝病的共存,而AIH / PBG重叠综合征是最常见的形式,几乎影响了10%的AIH或PBG患者[2],尽管AIH或PBG并存已经单独报道了多种其他自身免疫性疾病,在AIH / PBG重叠的情况下,这种关联的报道很少。在本文中,我们描述了与膜性肾小球肾炎(MGN)相关的AIH / PBG重叠病例,其在泼尼松龙,硫唑嘌呤(AZT)和熊去氧胆酸(UDCA)治疗后其肾脏和肝脏病变得以解决。

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