C3 Glomerulonephritis Associated with Monoclonal Gammopathy.

IF 0.8 Q4 UROLOGY & NEPHROLOGY
Indian Journal of Nephrology Pub Date : 2024-11-01 Epub Date: 2024-06-17 DOI:10.25259/ijn_543_23
Ana D Piedade, Patricia A Domingues, António S Inácio, Beatriz B Mendes, Lúcia F Parreira
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引用次数: 0

Abstract

C3 glomerulonephritis (C3GN) is rare. It is a proliferative glomerulonephritis resulting from glomerular deposition of complement factors due to dysregulation of the alternative pathway of complement. The association between monoclonal protein production and development of C3GN was described. We report a 74-year-old man with rapid worsening of kidney function and dialysis needed due to C3GN. In this case, serum protein electrophoresis showed no monoclonal spike but serum immunoelectrophoresis showed a lambda light chain monoclonal gammopathy. Once the diagnosis was made, the patient was treated with immunosuppression with complete kidney recovery. This case shows the importance of accurate and prompt diagnosis and appropriate treatment.

C3肾小球肾炎伴单克隆γ病。
C3 肾小球肾炎(C3GN)十分罕见。它是一种增殖性肾小球肾炎,由于补体的替代途径失调,导致补体因子在肾小球沉积。单克隆蛋白的产生与 C3GN 的发展之间存在关联。我们报告了一名因 C3GN 导致肾功能迅速恶化并需要透析的 74 岁男性患者。在该病例中,血清蛋白电泳显示没有单克隆尖峰蛋白,但血清免疫电泳显示有λ轻链单克隆丙种球蛋白病。确诊后,患者接受了免疫抑制治疗,肾脏完全康复。这一病例表明了准确、及时诊断和适当治疗的重要性。
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来源期刊
Indian Journal of Nephrology
Indian Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
1.40
自引率
0.00%
发文量
128
审稿时长
24 weeks
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