Müller-Höcker J, Weiss M, Thoenes G H, Grund A, Nerlich A
Pathologisches Institut, Ludwig-Maximilians-Universität, Munich, Germany.
Pathol Res Pract. 2002;198(5):375-9. doi: 10.1078/0344-0338-00269.
A case of idiopathic nodular glomerulosclerosis mimicking diabetic Kimmelstiel-Wilson glomerulopathy is reported. The patient was a 45-year-old man suffering from nephrotic syndrome. Light and electron microscopy revealed diffuse and nodular glomerulosclerosis indistinguishable from diabetic nodular glomerulosclerosis. Diabetes mellitus, however, had been excluded both by extensive clinical and by laboratory investigation. The differential diagnosis also included amyloidotic and non-amyloidotic fibrillary glomerulopathy, light chain glomerulopathy, collagen type III disease, immunotactoid glomerulopathy, and the sclerosing variant of membranoproliferative glomerulonephritis. Immunohistochemistry and ultrastructural investigations, however, excluded these entities, and the diagnosis of idiopathic nodular glomerulosclerosis was made. This variant has to be included in the differential diagnosis of nodular glomerulopathy associated with nephrotic syndrome.
报告了一例酷似糖尿病性结节性肾小球硬化症的特发性结节性肾小球硬化症病例。患者为一名45岁患有肾病综合征的男性。光镜和电镜检查显示弥漫性和结节性肾小球硬化,与糖尿病结节性肾小球硬化难以区分。然而,通过广泛的临床和实验室检查已排除糖尿病。鉴别诊断还包括淀粉样和非淀粉样纤维性肾小球病、轻链肾小球病、III型胶原病、免疫触须样肾小球病以及膜增生性肾小球肾炎的硬化变异型。然而,免疫组化和超微结构检查排除了这些疾病,从而做出了特发性结节性肾小球硬化症的诊断。这种变异型必须纳入肾病综合征相关结节性肾小球病的鉴别诊断中。