Mota-Hernández F, Briseño-Mondragón E, Gordillo-Paniagua G
Nephron. 1976;16(4):272-81. doi: 10.1159/000180611.
131 children with nephritic syndrome of acute onset were studied by renal biopsy and were followed clinically from 2 to 13 years. 87 patients (66%) with proliferative endocapillary glomerulonephritis all recovered. 21 (16%) had focal extracapillary and diffuse endocapillary glomerulonephritis. Eleven (52%) of these recovered. Six patients (5%) had diffuse extra and endocapillary glomerulonephritis, 13 (10%) had membrano-proliferative glomerulonephritis and four had diffuse glomerular fibrosis. All 23 patients of the latter groups progressed to renal insufficiency. A correlation between morphology and prognosis was apparent in this study.
对131例急性起病的肾病综合征患儿进行了肾活检,并进行了为期2至13年的临床随访。87例(66%)毛细血管内增生性肾小球肾炎患者均康复。21例(16%)患有局灶性毛细血管外和弥漫性毛细血管内肾小球肾炎。其中11例(52%)康复。6例(5%)患有弥漫性毛细血管外和毛细血管内肾小球肾炎,13例(10%)患有膜增生性肾小球肾炎,4例患有弥漫性肾小球纤维化。后几组的所有23例患者均进展为肾功能不全。本研究中形态学与预后之间的相关性明显。