A Rare Case of Renal Thrombotic Microangiopathy and Focal Segmental Glomerulosclerosis Secondary to Plasma Cell Leukemia.

IF 0.7 Q4 HEMATOLOGY Case Reports in Hematology Pub Date : 2023-01-01 DOI:10.1155/2023/7803704
Justin Komisarof, Jessica Forman, Bruce Goldman, Chauncey Syposs, Frank Passero, Ellie Garbade
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Abstract

Plasma cell dyscrasias are a subset of hematological malignancies involving the production of monoclonal immunoglobulins. This spectrum of disorders includes asymptomatic conditions such as monoclonal gammopathy of unknown significance as well as extremely aggressive malignancies such as plasma cell leukemia. Monoclonal gammopathies are occasionally associated with renal failure, which can occur via many pathophysiological processes. The most common of these is light chain cast nephropathy, but many rare renal complications exist, including thrombotic microangiopathy (TMA) and focal segmental glomerulosclerosis (FSGS). Here, we report a patient with new renal failure with features of TMA and FSGS on biopsy and found to be secondary to plasma cell leukemia.

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继发于浆细胞白血病的肾血栓性微血管病和局灶节段性肾小球硬化1例。
浆细胞异常是血液学恶性肿瘤的一个子集,涉及单克隆免疫球蛋白的产生。这一系列疾病包括无症状的情况,如意义不明的单克隆伽玛病,以及极具侵袭性的恶性肿瘤,如浆细胞白血病。单克隆伽玛病偶尔与肾功能衰竭相关,可通过许多病理生理过程发生。其中最常见的是轻链铸造肾病,但也存在许多罕见的肾脏并发症,包括血栓性微血管病(TMA)和局灶节段性肾小球硬化(FSGS)。在这里,我们报告了一例新的肾衰患者,活检显示TMA和FSGS的特征,发现继发于浆细胞白血病。
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发文量
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审稿时长
13 weeks
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