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Renal complications in chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis: the Mayo Clinic experience

机译:慢性淋巴细胞性白血病和单克隆B细胞淋巴细胞增多症的肾脏并发症:梅奥诊所的经验

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摘要

While the renal complications of plasma cell dyscrasia have been well-described, most information in patients with chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis is derived from case reports. This is a retrospective analysis of patients with chronic lymphocytic leukemia or monoclonal B-cell lymphocytosis who underwent kidney biopsy for renal insufficiency and/or nephrotic syndrome. Between January 1995 and June 2014, 49 of 4,024 (1.2%) patients with chronic lymphocytic leukemia (n=44) or monoclonal B-cell lymphocytosis (n=5) had a renal biopsy: 34 (69%) for renal insufficiency and 15 (31%) for nephrotic syndrome. The most common findings on biopsy were: membranoproliferative glomerulonephritis (n=10, 20%), chronic lymphocytic leukemia interstitial infiltration as primary etiology (n=6, 12%), thrombotic microangiopathy (n=6, 12%), and minimal change disease (n=5, 10%). All five membranoproliferative glomerulonephritis patients treated with rituximab, cyclophosphamide and prednisone-based regimens had recovery of renal function compared to 0/3 patients treated with rituximab with or without steroids. Chronic lymphocytic leukemia infiltration as the primary cause of renal abnormalities was typically observed in relapsed/refractory patients (4/6). Thrombotic microangiopathy primarily occurred as a treatment-related toxicity of pentostatin (4/6 cases), and resolved with drug discontinuation. All cases of minimal change disease resolved with immunosuppressive agents only. Renal biopsy plays an important role in the management of patients with chronic lymphocytic leukemia or monoclonal B-cell lymphocytosis who develop renal failure and/or nephrotic syndrome.
机译:尽管已经很好地描述了浆细胞发育不良的肾脏并发症,但慢性淋巴细胞性白血病和单克隆B细胞淋巴细胞增多症患者的大多数信息均来自病例报告。这是对因肾功能不全和/或肾病综合征而接受肾脏活检的慢性淋巴细胞性白血病或单克隆B细胞淋巴细胞增多症患者的回顾性分析。在1995年1月至2014年6月之间,在4,024名(1.2%)慢性淋巴细胞性白血病(n = 44)或单克隆B细胞淋巴细胞增多症(n = 5)的患者中,进行了肾活检:肾功能不全34例(69%),15例(31%)为肾病综合症。活检最常见的发现是:膜增生性肾小球肾炎(n = 10,20%),慢性淋巴细胞性白血病作为主要病因的间质浸润(n = 6,12%),血栓性微血管病(n = 6,12%)和最小的改变疾病(n = 5,10%)。与使用或不使用类固醇的利妥昔单抗治疗的0/3患者相比,接受利妥昔单抗,环磷酰胺和泼尼松治疗的所有五名膜增生性肾小球肾炎患者的肾功能均得到恢复。慢性淋巴细胞白血病浸润是肾脏异常的主要原因,通常在复发/难治患者中观察到(4/6)。血栓性微血管病主要发生在喷喷他汀的治疗相关毒性反应中(4/6例),并通过停药解决。所有轻微变化疾病的病例都只能用免疫抑制剂解决。肾活检在患有肾功能衰竭和/或肾病综合征的慢性淋巴细胞性白血病或单克隆B细胞淋巴细胞增多症患者的治疗中起着重要作用。

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