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Transition from endocapillary proliferative glomerulonephritis to membranoproliferative glomerulonephritis in a patient with a prolonged human parvovirus B19 infection

机译:人类细小病毒B19感染时间延长的患者从毛细血管内增生性肾小球肾炎转变为膜增生性肾小球肾炎

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We report a case in which renal biopsies were performed 4 years apart in a woman with a prolonged human parvovirus B19 (HPB19) infection. When she was 29 years old the first biopsy, performed because of microscopic hematuria and mild proteinuria, showed endocapillary and mesangial proliferative glomerulonephritis in light microscopy as well as deposits of immunoglobulins (Igs) and complement C3 on capillary walls. Mesangial, intramembranous, and subepithelial hump-like electron dense deposits were seen in electron microscopy. The principal differential diagnoses, acute poststreptococcal glomerulonephritis and lupus nephritis, were unlikely, and her serological positivity for IgM antibody for HPB19 made us diagnose acute glomerulonephritis associated with HPB19 infection. The second biopsy, performed 4 years later because of persistent proteinuria and prolonged positivity for IgM antibody for HPB19, showed membranoproliferative glomerulonephritis (MPGN) with mesangial interposition and with thickening and double contours of glomerular basement membrane. In tissues obtained in both biopsies, HPB19 DNA was detected by polymerase chain reaction. HPB19 infection has been widely known to cause various glomerular diseases. This case reveals that acute endocapillary proliferative glomerulonephritis can change into MPGN during prolonged HPB19 infection.
机译:我们报告了一个案例,其中一名人类细小病毒B19(HPB19)感染时间延长的女性每隔4年进行一次肾脏活检。当她29岁时,由于显微镜下的血尿和轻度蛋白尿而进行的首次活检在光学显微镜下显示了毛细血管内膜和系膜增生性肾小球肾炎,以及在毛细血管壁上沉积了免疫球蛋白(Igs)和补体C3。在电子显微镜下可见肾小球膜,膜内和上皮下的驼峰状电子致密沉积物。主要的鉴别诊断是急性链球菌性肾小球性肾炎和狼疮性肾炎,可能性不大,她对HPB19的IgM抗体的血清学阳性使我们得以诊断与HPB19感染有关的急性肾小球性肾炎。由于持续的蛋白尿和对HPB19的IgM抗体的延长阳性而在4年后进行的第二次活检显示膜增生性肾小球肾炎(MPGN)伴有肾小球膜夹层,肾小球基底膜增厚和双轮廓。在两次活检中获得的组织中,通过聚合酶链反应检测到HPB19 DNA。众所周知,HPB19感染会引起各种肾小球疾病。该病例表明,在延长的HPB19感染期间,急性毛细血管内增生性肾小球肾炎可转变为MPGN。

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