Hogg R J, Savino D A
Department of Pediatrics, Baylor University Medical Center, Dallas, TX 75246.
Pediatr Nephrol. 1990 Jan;4(1):36-8. doi: 10.1007/BF00858435.
A patient with spontaneous remission of nephrotic syndrome (NS) associated with IgA nephropathy is described. The patient presented at the age of 8 years with asymptomatic proteinuria, and at the age of 11 years developed classical features of NS. A percutaneous renal biopsy showed mild mesangial prominence without significant hypercellularity, electron-dense deposits within the mesangium, and 3+ mesangial staining with IgA and IgG. NS resolved 6 weeks after onset without any form of therapy; absence of proteinuria persisted 6 months later. This report demonstrates clearly that patients with NS associated with IgA nephropathy may undergo spontaneous resolution of their proteinuria.
本文描述了一名患有与IgA肾病相关的肾病综合征(NS)且病情自发缓解的患者。该患者8岁时出现无症状蛋白尿,11岁时出现NS的典型症状。经皮肾活检显示轻度系膜突出,无明显细胞增多,系膜内有电子致密沉积物,系膜IgA和IgG染色为3+。NS在发病6周后未经任何形式的治疗即缓解;6个月后仍无蛋白尿。本报告清楚地表明,患有与IgA肾病相关的NS的患者可能会自发缓解蛋白尿。