Velásquez-Jones L, Sánchez-Aguilar J R, Ramòn-Garcia G, Rosado-Tun M A, Romero-Navarro B, Gómez-Chico R, Muñoz-Arizpe R
Departamento de Nefrología, Hospital Infantil de México Federico Gómez, D.F.
Bol Med Hosp Infant Mex. 1992 Dec;49(12):832-8.
IgA nephropathy, also called Berger's disease, is characterized by recurrent gross hematuria or persistent microscopic hematuria, together with mesangial glomerular deposits of IgA found in the renal biopsy. Seven children with IgA nephropathy were studied. Most of them presented initially with recurrent macroscopic hematuria and low or moderate-grade proteinuria, without hypertension or renal function impairment. Only one patient presented with a rapidly progressive glomerulonephritis. Four patients did not receive any treatment; one of them is in remission, one has improved and two remain with moderate proteinuria and hematuria. One patient with significant proteinuria improved after prednisone and azathioprine treatment. The patient with rapidly progressive glomerulonephritis improved his renal function after oral prednisone and intravenous boluses of methylprednisolone and cyclophosphamide.
IgA肾病,也称为伯杰氏病,其特征为反复肉眼血尿或持续性镜下血尿,同时在肾活检中发现肾小球系膜有IgA沉积。对7例IgA肾病患儿进行了研究。他们大多最初表现为反复肉眼血尿和轻度或中度蛋白尿,无高血压或肾功能损害。只有1例患者表现为快速进展性肾小球肾炎。4例患者未接受任何治疗;其中1例缓解,1例病情改善,2例仍有中度蛋白尿和血尿。1例有大量蛋白尿的患者在泼尼松和硫唑嘌呤治疗后病情改善。快速进展性肾小球肾炎患者在口服泼尼松、静脉推注甲泼尼龙和环磷酰胺后肾功能得到改善。