隐性老虎:抗肾小球基底膜病的非典型表现

A. Lecamwasam, Darren Lee, A. Skene, L. McMahon
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引用次数: 0

摘要

抗肾小球基底膜疾病的特征是免疫球蛋白G (IgG)沿肾小球基底膜呈线性沉积。抗gbm疾病与另一种类型的肾小球肾炎的并发已被很好地描述。我们报告一例坏死性肾小球肾炎,伴有前体全身性症状,肾功能恶化速度低于预期,并且存在循环抗gbm抗体。最初根据免疫组化(IHC)染色在组织学上诊断为免疫球蛋白A (IgA)肾病,但随后活检的免疫荧光(IF)染色更符合抗gbm疾病并共存轻度IgA肾病的诊断。及时开始标准治疗抗gbm疾病使肾功能正常化。本病例强调抗gbm疾病可以表现为非典型,也可能与另一种形式的肾小球肾炎共存。世界肾脏病杂志,2014;3(3):124-128 doi: http://dx.doi.org/10.14740/wjnu173w
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hidden Tiger: An Atypical Presentation of Anti-Glomerular Basement Membrane Disease
Anti-glomerular basement membrane (anti-GBM) disease is characterized by linear deposition of immunoglobulin G (IgG) along the GBM. The concurrence of anti-GBM disease with another type of glomerulonephritis has been well described. We report a case of necrotizing glomerulonephritis in association with prodromal systemic symptoms, deterioration in kidney function less rapid than expected, and the presence of circulating anti-GBM antibody. This was initially diagnosed histologically as immunoglobulin A (IgA) nephropathy based on immunohistochemistry (IHC) staining, but immunofluorescence (IF) staining on a subsequent biopsy was more consistent with a diagnosis of anti-GBM disease with co-existing mild IgA nephropathy. Prompt initiation of standard treatment of anti-GBM disease normalized kidney function. This case highlights that anti-GBM disease can present atypically and may also co-exist with another form of glomerulonephritis. World J Nephrol Urol. 2014;3(3):124-128 doi: http://dx.doi.org/10.14740/wjnu173w
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