Centre national de référence maladies rares amylose AL et autres maladies à dépôts d'immunoglobulines monoclonales, CHU Poitiers, Université de Poitiers, Poitiers, France; Department of Nephrology, Hôpital Jean Bernard, CHU Poitiers, Université de Poitiers, Poitiers, France.
Centre national de référence maladies rares amylose AL et autres maladies à dépôts d'immunoglobulines monoclonales, CHU Poitiers, Université de Poitiers, Poitiers, France; Department of Nephrology, Hôpital Jean Bernard, CHU Poitiers, Université de Poitiers, Poitiers, France; CNRS UMR 6101, Université de Limoges, Limoges, France.
Am J Kidney Dis. 2015 Nov;66(5):756-67. doi: 10.1053/j.ajkd.2015.03.035. Epub 2015 May 16.
Kidney diseases associated with immunoglobulin M (IgM) monoclonal gammopathy are poorly described, with few data for patient outcomes and renal response.
Case series.
SETTING & PARTICIPANTS: 35 patients from 8 French departments of nephrology were retrospectively studied. Inclusion criteria were: (1) detectable serum monoclonal IgM, (2) estimated glomerular filtration rate (eGFR) < 60mL/min/1.73m(2) and/or proteinuria with protein excretion > 0.5g/d and/or microscopic hematuria, and (3) kidney biopsy showing monoclonal immunoglobulin deposits and/or lymphomatous B-cell renal infiltration. All patients received chemotherapy, including rituximab-based regimens in 8 cases.
Patients were classified into 3 groups according to renal pathology: glomerular AL amyloidosis (group 1; n=11), nonamyloid glomerulopathies (group 2; n=15, including 9 patients with membranoproliferative glomerulonephritis), and tubulointerstitial nephropathies (group 3; n=9, including cast nephropathy in 5, light-chain Fanconi syndrome in 3, and isolated tumor infiltration in 1).
Posttreatment hematologic response (≥50% reduction in serum monoclonal IgM and/or free light chain level) and renal response (≥50% reduction in 24-hour proteinuria or eGFR≥30mL/min/1.73m(2) in patients with glomerular and tubulointerstitial disorders, respectively).
Nephrotic syndrome was observed in 11 and 6 patients in groups 1 and 2, respectively. Patients in group 3 presented with acute kidney injury (n=7) and/or proximal tubular dysfunction (n=3). Waldenström macroglobulinemia was present in 26 patients (8, 12, and 6 in groups 1, 2, and 3, respectively). Significant lymphomatous interstitial infiltration was observed in 18 patients (4, 9, and 5 patients, respectively). Only 9 of 29 evaluable patients had systemic signs of symptomatic hematologic disease (2, 5, and 2, respectively). In groups 1, 2, and 3, respectively, hematologic response was achieved after first-line treatment in 3 of 9, 9 of 10, and 5 of 6 evaluable patients, while renal response occurred in 5 of 10, 9 of 15, and 5 of 8 evaluable patients.
Retrospective study; insufficient population to establish the impact of chemotherapy.
IgM monoclonal gammopathy is associated with a wide spectrum of renal manifestations, with an under-recognized frequency of tubulointerstitial disorders.
与免疫球蛋白 M (IgM) 单克隆丙种球蛋白病相关的肾脏疾病描述不佳,患者结局和肾脏反应的数据较少。
病例系列。
来自法国 8 个肾病部门的 35 名患者进行了回顾性研究。纳入标准为:(1)可检测到血清单克隆 IgM;(2)估算肾小球滤过率 (eGFR) < 60mL/min/1.73m2 和/或蛋白尿> 0.5g/d 和/或镜下血尿;(3)肾活检显示单克隆免疫球蛋白沉积和/或淋巴样 B 细胞肾浸润。所有患者均接受化疗,8 例患者接受利妥昔单抗为基础的方案。
根据肾脏病理将患者分为 3 组:肾小球 AL 淀粉样变性 (组 1;n=11)、非淀粉样变性肾小球病 (组 2;n=15,包括 9 例膜增殖性肾小球肾炎) 和肾小管间质性肾病 (组 3;n=9,包括 5 例铸型肾病、3 例轻链 Fanconi 综合征和 1 例孤立性肿瘤浸润)。
治疗后血液学反应 (血清单克隆 IgM 和/或游离轻链水平降低≥50%) 和肾脏反应 (肾小球和肾小管间质性疾病患者的 24 小时蛋白尿减少≥50%或 eGFR≥30mL/min/1.73m2)。
1 组和 2 组分别有 11 例和 6 例患者出现肾病综合征。组 3 的 7 例患者出现急性肾损伤和/或近端肾小管功能障碍,3 例患者出现近端肾小管功能障碍。26 例患者存在华氏巨球蛋白血症 (分别为组 1、2 和 3 的 8、12 和 6 例)。18 例患者存在显著的淋巴瘤间质浸润 (分别为组 1、2 和 3 的 4、9 和 5 例)。29 例可评估患者中仅 9 例有全身症状性血液系统疾病的迹象 (分别为组 1、2 和 3 的 2、5 和 2 例)。组 1、2 和 3 中,9 例可评估患者中分别有 3 例、10 例中的 9 例和 6 例中的 5 例在一线治疗后获得血液学反应,10 例可评估患者中分别有 5 例、15 例中的 9 例和 8 例可评估患者中的 5 例获得肾脏反应。
回顾性研究;人群不足,无法确定化疗的影响。
IgM 单克隆丙种球蛋白病与广泛的肾脏表现相关,肾小管间质性疾病的频率被低估。