Suppr超能文献

马来西亚患者群体中原发性IgA肾病的组织病理学模式。

The histopathological pattern of primary IgA nephropathy in a Malaysian patient population.

作者信息

Peh S C, Looi L M, Wang F, Chua C T, Tan H W, Lam K L

机构信息

Department of Pathology, Faculty of Medicine, University of Malaya, Kuala Lumpur.

出版信息

Malays J Pathol. 1990 Jun;12(1):21-6.

PMID:2090886
Abstract

In the 10-year period from October 1977 to July 1987, 149 cases of primary IgA nephropathy were histologically confirmed through renal biopsies in the Department of Pathology, University Hospital, Kuala Lumpur. The ages of these patients ranged from 5 to 72 years, with the majority in the 20-30 year age group. There was no sex preponderance. The ethnic distribution showed a significant predominance of Chinese with 107 (71.8%) Chinese, 24 (16.1%) Malays, 15 (10.1%) Indians and 3 others. A wide range of renal glomerular pathology was seen, the commonest being diffuse mesangioproliferative glomerulonephritis (59.1%). Focal proliferative glomerulonephritis (14.1%) followed by minimal change glomerulonephritis (10.7%) were next in order of frequency. Immunofluorescence studies consistently demonstrated heavy and predominant IgA deposition in the mesangium. Weak deposition of C3, IgG and IgM were also observed in various combinations.

摘要

在1977年10月至1987年7月的10年期间,吉隆坡大学医院病理科通过肾活检组织学确诊了149例原发性IgA肾病。这些患者的年龄在5岁至72岁之间,大多数在20至30岁年龄组。没有性别优势。种族分布显示,华人占显著多数,其中华人107例(71.8%),马来人24例(16.1%),印度人15例(10.1%),其他3例。可见广泛的肾小球病理改变,最常见的是弥漫性系膜增生性肾小球肾炎(59.1%)。局灶性增生性肾小球肾炎(14.1%)其次是微小病变性肾小球肾炎(10.7%),按频率排列居次。免疫荧光研究一致显示系膜中有大量且主要的IgA沉积。还观察到C3、IgG和IgM以各种组合方式出现弱阳性沉积。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验