Jennette J C, Newman W J, Diaz-Buxo J A
Am J Clin Pathol. 1987 Jul;88(1):74-8. doi: 10.1093/ajcp/88.1.74.
Four patients with overlapping IgA nephropathy and membranous nephropathy recently have been reported from two different medical centers in Japan. The authors describe two patients from the United States with the concurrence of IgA and membranous nephropathy and a third patient who may have the same overlapping glomerular lesions. All three patients had hematuria and nephrotic range proteinuria. Renal biopsy specimens from two of the patients revealed focal proliferative glomerular lesions, large mesangial and numerous subepithelial electron-dense deposits, exclusively mesangial intense immunostaining for IgA, and extensive granular capillary wall immunostaining for IgG. The third patient is a sibling of one of the other patients and was shown to have focal proliferative glomerular lesions, mesangial immunostaining for IgA, and numerous subepithelial electron-dense deposits. Pathogenic possibilities are discussed.
日本两个不同医疗中心最近报告了4例重叠性IgA肾病和膜性肾病患者。作者描述了来自美国的2例同时患有IgA和膜性肾病的患者,以及第3例可能具有相同重叠性肾小球病变的患者。所有3例患者均有血尿和肾病范围蛋白尿。其中2例患者的肾活检标本显示局灶性增生性肾小球病变、大的系膜和大量上皮下电子致密沉积物、仅系膜IgA强免疫染色以及广泛的毛细血管壁IgG颗粒状免疫染色。第3例患者是另外1例患者的兄弟姐妹,显示有局灶性增生性肾小球病变、系膜IgA免疫染色和大量上皮下电子致密沉积物。文中讨论了致病的可能性。