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成人原发性肾小球疾病的患病率:对206例肾活检的回顾性分析(1990 - 1993年)

Prevalence of adult primary glomerular diseases: retrospective analysis of 206 kidney biopsies (1990-1993).

作者信息

Mazzarolo Cruz H M, Cruz J, Silva A L, Saldanha L B, de Oliveira Penna D

机构信息

Department of Internal Medicine, University of São Paulo School of Medicine, Brazil.

出版信息

Rev Hosp Clin Fac Med Sao Paulo. 1996 Jan-Feb;51(1):3-6.

PMID:8762646
Abstract

The prevalences of the various histopathologic forms of primary glomerular disease (PGD) were evaluated by the retrospective analysis of 206 kidney biopsies performed in a three-year period (september 1990-september 1993) in patients between 14 and 73 years of age (107 men and 99 women). Data were compared with those of a study conducted in 1985-1987, on patients of the same age group. In the present study, primary glomerular diseases showed the following prevalences: focal glomerulosclerosis, 43.2%; membranous GN, 20.4%; membranoproliferative GN, 14.1%; IgA nephropathy, 10.2%; minimal-change disease, 5.3%; mesangioproliferative GN, 2.9%; acute diffuse GN, 1.9%; rapidly progressive GN and proliferative focal segmental GN, 1% each one. Prevalences were similar in both sexes. Primary glomerular diseases were significantly more prevalent in patients with 35 years or less than in those up this age (64.6% vs 34.4%). Nonproliferative primary glomerular diseases were significantly more prevalent than the proliferative forms (68.9% vs 31.1%). The prevalences of the various histopathologic of PGD, with few exceptions, were about similar in the periods 1985-1987 and 1990-1993: the prevalences of focal glomerulosclerosis, membranous GN, IgA nephropathy and mesangioproliferative GN showed no significant differences; the prevalence of membranoproliferative GN increased (6.8% vs 14.1%), but that of type II remained very low (0.5%). Focal glomerulosclerosis was the most prevalent PGD. The prevalence of IgA nephropathy remained low, comparable with the smallest prevalences found in some of the Western countries.

摘要

通过对1990年9月至1993年9月三年间对14至73岁患者(107名男性和99名女性)进行的206例肾活检进行回顾性分析,评估了原发性肾小球疾病(PGD)各种组织病理学形式的患病率。将数据与1985 - 1987年对同一年龄组患者进行的一项研究的数据进行了比较。在本研究中,原发性肾小球疾病的患病率如下:局灶性肾小球硬化症,43.2%;膜性肾小球肾炎,20.4%;膜增生性肾小球肾炎,14.1%;IgA肾病,10.2%;微小病变病,5.3%;系膜增生性肾小球肾炎,2.9%;急性弥漫性肾小球肾炎,1.9%;急进性肾小球肾炎和增生性局灶节段性肾小球肾炎,各为1%。两性患病率相似。35岁及以下患者原发性肾小球疾病的患病率显著高于该年龄以上患者(64.6%对34.4%)。非增生性原发性肾小球疾病的患病率显著高于增生性形式(68.9%对31.1%)。PGD各种组织病理学形式的患病率,除少数例外,在1985 - 1987年和1990 - 1993年期间大致相似:局灶性肾小球硬化症、膜性肾小球肾炎、IgA肾病和系膜增生性肾小球肾炎的患病率无显著差异;膜增生性肾小球肾炎的患病率有所增加(6.8%对14.1%),但II型的患病率仍然很低(0.5%)。局灶性肾小球硬化症是最常见的PGD。IgA肾病的患病率仍然较低,与一些西方国家发现的最低患病率相当。

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