增生性肾小球肾炎伴单克隆免疫球蛋白沉积,伪装成肾脏特异性血栓性微血管病。

IF 0.6 Q3 MEDICINE, GENERAL & INTERNAL BMJ Case Reports Pub Date : 2025-04-02 DOI:10.1136/bcr-2024-264201
Hayley J Duxbury, Vincent W Lee, Fiona Kwok, Seethalakshmi Viswanathan
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引用次数: 0

摘要

伴单克隆免疫球蛋白沉积的增生性肾小球肾炎是一种具有肾脏意义的单克隆伽玛病,很少与血栓性微血管病(TMA)同时发生。我们报告一例罕见的肾病综合征患者,其肾活检显示TMA和潜在的粒状电子致密沉积物主要沿着肾小球基底膜和系膜的内皮下面。蛋白酶消化、福尔马林固定、石蜡包埋切片的免疫荧光显示IgG3 kappa轻链限制。进一步的临床、放射学和血液学检查显示没有任何潜在的肿瘤b细胞或浆细胞克隆的证据。在多学科团队的投入下,患者接受硼替佐米和血浆置换治疗,使其长期临床稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Proliferative glomerulonephritis with monoclonal immunoglobulin deposits masquerading as renal-specific thrombotic microangiopathy.

Proliferative glomerulonephritis with monoclonal immunoglobulin deposits is a form of monoclonal gammopathy of renal significance that can rarely co-occur with thrombotic microangiopathy (TMA). We report a rare case in a patient who presented with nephrotic syndrome, in whom the renal biopsy showed TMA and underlying granular electron-dense deposits predominantly along the subendothelial aspect of the glomerular basement membrane and mesangium. Immunofluorescence performed on proteinase-digested formalin-fixed, paraffin-embedded sections showed IgG3 kappa light chain restriction. Further clinical, radiologic and haematologic investigations showed no evidence of any underlying neoplastic B-cell or plasma cell clone. Following multidisciplinary team input, the patient was treated with bortezomib and plasma exchange, allowing long-term clinical stabilisation.

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来源期刊
BMJ Case Reports
BMJ Case Reports Medicine-Medicine (all)
CiteScore
1.40
自引率
0.00%
发文量
1588
期刊介绍: BMJ Case Reports is an important educational resource offering a high volume of cases in all disciplines so that healthcare professionals, researchers and others can easily find clinically important information on common and rare conditions. All articles are peer reviewed and copy edited before publication. BMJ Case Reports is not an edition or supplement of the BMJ.
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