Immune Complex-Mediated Membranoproliferative Glomerulonephritis Secondary to Primary Biliary Cholangitis: A Rare Case Report

Kadir Intas, G. Okyay, A. Sağlam, M. Aylı
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Abstract

Immune complex-mediated membranoproliferative glomerulonephritis (iMPGN) can develop in association with autoimmune diseases such as primary biliary cholangitis (PBC), a chronic cholestatic liver disease characterised by destruction of the small and medium-sized bile ducts. Although the pathogenesis cannot be clearly defined, iMPGN and PBC overlap through the activation of innate and adaptive immune cells and the production of proinflammatory mediators. In this report, the authors present a case in which iMPGN and PBC were diagnosed simultaneously.
继发于原发性胆汁性胆管炎的免疫复合物介导的膜增生性肾小球肾炎:罕见病例报告
免疫复合物介导的膜增生性肾小球肾炎(iMPGN)可与原发性胆汁性胆管炎(PBC)等自身免疫性疾病同时发生,原发性胆汁性胆管炎是一种慢性胆汁淤积性肝病,其特点是中小型胆管遭到破坏。虽然发病机制尚不明确,但 iMPGN 和 PBC 通过激活先天性和适应性免疫细胞以及产生促炎介质而相互重叠。在本报告中,作者介绍了一例同时诊断出 iMPGN 和 PBC 的病例。
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