A Rare Case of Polyneuropathy and Monoclonalgammopathy with Recurrent Acute Kidney Injury.

Q3 Medicine
Electrolyte and Blood Pressure Pub Date : 2016-06-01 Epub Date: 2016-06-30 DOI:10.5049/EBP.2016.14.1.5
Eun Jung Kim, Dong Ho Shin, Hee Jung Jeon, So Yon Rhee, Eun Sook Nam, Ji Young Park, Jieun Oh
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引用次数: 2

Abstract

POEMS syndrome is a rare paraneoplastic syndrome and there are few reports of polyneuropathy and monoclonal gammopathy associated with kidney dysfunction. Here, we report a case of POEMS syndrome with recurrent acute kidney injury (AKI). A 52-year-old man presented with bilateral aggravating paresthesia and latermotor weakness of the lower extremities accompanied by repeated elevation of serum creatinine. The patient was finally diagnosed with POEMS syndrome on the basis of fulfilling the two mandatory major criteria (polyneuropathy and monoclonal gammopathy), one other major criterion (sclerotic bone lesion), and several minor criteria. A renal biopsy was performed to clarify the cause of AKI and showed membranoproliferative glomerulonephritis-like lesions with mesangiolysis and endothelial cell injury. This case illustrates that renal manifestations, not included in the diagnostic criteria for POEMS, can be apparent before various other systemic symptoms.

Abstract Image

Abstract Image

Abstract Image

罕见的多发性神经病变和单克隆神经症并发复发性急性肾损伤1例。
POEMS综合征是一种罕见的副肿瘤综合征,与肾功能不全相关的多神经病变和单克隆γ病变的报道很少。在此,我们报告一例POEMS综合征合并复发性急性肾损伤(AKI)。52岁男性患者表现为双侧加重的感觉异常和下肢外侧运动无力,伴血清肌酐反复升高。在满足两项强制性主要标准(多发性神经病变和单克隆伽玛病)、另一项主要标准(硬化性骨病变)和几项次要标准的基础上,患者最终被诊断为POEMS综合征。为了明确AKI的病因,进行了肾活检,结果显示膜增生性肾小球肾炎样病变伴血管松解和内皮细胞损伤。本病例说明肾表现,不包括在POEMS的诊断标准中,可以在各种其他全身性症状之前出现。
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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来源期刊
Electrolyte and Blood Pressure
Electrolyte and Blood Pressure Medicine-Internal Medicine
CiteScore
2.10
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