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[I型和III型膜增生性肾小球肾炎。临床表现与预后]

[Type I and III membranoproliferative glomerulonephritis. Clinical picture and prognosis].

作者信息

Matousovic K, Rossmann P, Prát V, Chadimová M

机构信息

Program výzkumu transplantací orgánů, Institutu klinické a experimentální medicíny, Praha.

出版信息

Cas Lek Cesk. 1990 Jun 22;129(25):778-81.

PMID:2393885
Abstract

Membranoproliferative glomerulonephritis (CN) of types I and III was diagnosed in 154 patients (15.5% out of primary CN). Out of this number 60% were men. During biopsy, one third of the patients were normotensive, 40% were slightly hypertensive and one third suffered from severe hypertension. Mean proteinuria was 6.5 +/- 5.5 g/24 h. In two thirds of the patients erythrocyturia was higher than 35 mil. in Addis' sediment and the findings in the urine were characterised by the proportion between proteinuria and erythrocyturia (p less than 0.001). During biopsy in one half of the patients, the serum creatinine level was already elevated. The presence of creatininemia was found to be directly linked to blood pressure, proteinuria, the degrees of extracapillary proliferation, tubulointerstitial regression and vascular arteriolosclerosis. The cumulative duration of the kidney function within the period of 10-20 years was 41 or 28%, the cumulative cure amounted to 14% 10 years after biopsy.

摘要

154例患者被诊断为I型和III型膜增生性肾小球肾炎(CN)(占原发性CN的15.5%)。其中60%为男性。活检时,三分之一的患者血压正常,40%轻度高血压,三分之一患有重度高血压。平均蛋白尿为6.5±5.5g/24小时。三分之二的患者红细胞尿高于3500万/艾迪计数,尿液检查结果以蛋白尿与红细胞尿的比例为特征(p<0.001)。活检时,一半患者的血清肌酐水平已升高。发现肌酐血症与血压、蛋白尿、毛细血管外增生程度、肾小管间质退变和血管小动脉硬化直接相关。10至20年期间肾功能的累积持续时间为41%或28%,活检后10年累积治愈率为14%。

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