Kebler R, Kithier K, McDonald F D, Cadnapaphornchai P
Am J Med. 1985 Jan;78(1):133-8. doi: 10.1016/0002-9343(85)90473-5.
A case of rapidly progressive glomerulonephritis associated with nephrotic syndrome, hematuria, and edema is reported. Monoclonal IgG-lambda was found in the serum and urine. Renal biopsy revealed diffuse proliferative glomerulonephritis with crescent formation. Immunofluorescent study revealed IgG and lambda in a focal segmental distribution. Subepithelial humps were found on electron microscopic examination. A spectacular feature of the deposits was the presence of organized linear fibrils within the humps. Similar fibrils were found in the mesangium and urinary space. Renal function deteriorated rapidly, necessitating hemodialysis in eight months. In addition to the present case, 24 cases of glomerulonephritis associated with "benign" monoclonal gammopathy reported since 1970 are reviewed, and the potential causal relationship between monoclonal gammopathy and glomerular involvement is stressed.
报告了一例与肾病综合征、血尿和水肿相关的快速进展性肾小球肾炎病例。血清和尿液中发现单克隆IgG-λ。肾活检显示弥漫性增生性肾小球肾炎伴新月体形成。免疫荧光研究显示IgG和λ呈局灶节段性分布。电子显微镜检查发现上皮下驼峰。沉积物的一个显著特征是驼峰内存在有组织的线性纤维。在系膜和尿腔中也发现了类似的纤维。肾功能迅速恶化,八个月内需要进行血液透析。除了本病例外,还回顾了自1970年以来报道的24例与“良性”单克隆丙种球蛋白病相关的肾小球肾炎病例,并强调了单克隆丙种球蛋白病与肾小球受累之间的潜在因果关系。