Division of Nephrology and Rheumatology, Department of Internal Medicine, Aichi Medical University School of Medicine, Nagakute-cyo, Aichi, 480-1195, Japan.
Clin Exp Nephrol. 2010 Feb;14(1):90-3. doi: 10.1007/s10157-009-0227-x. Epub 2009 Oct 1.
A 61-year-old man infected with hepatitis C virus developed urinary protein. Two-dimensional electrophoresis and immunoblotting of sera revealed no monoclonal proteins. Light microscopy and immunofluorescence of a kidney biopsy specimen demonstrated bubbling appearance and formation of spikes, associated with predominantly IgA1-lambda deposition, but not IgG, along glomerular capillary walls. Electron microscopy showed electron-dense deposits without any fibrillary structure located in the glomerular basement membrane. Seven months after the kidney biopsy, the patient had a surgical operation for rectal cancer. One year later, the urinary protein was still present. The present case is the first report of an IgA1-lambda-type monoclonal immunoglobulin deposition disease associated with membranous features.
一位 61 岁的男性感染丙型肝炎病毒后出现尿蛋白。血清的二维电泳和免疫印迹显示无单克隆蛋白。肾活检标本的光镜和免疫荧光检查显示冒泡外观和刺形成,主要与 IgA1-λ 沉积相关,但 IgG 不相关,沿肾小球毛细血管壁。电子显微镜显示电子致密沉积物,在肾小球基底膜中无任何纤维状结构。肾活检后 7 个月,患者接受直肠癌手术。一年后,尿蛋白仍然存在。本病例是首例与膜性特征相关的 IgA1-λ 型单克隆免疫球蛋白沉积病的报告。