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家族性肾炎和“良性”血尿中的肾小球基底膜变薄

Glomerular basement membrane attenuation in familial nephritis and "benign" hematuria.

作者信息

Piel C F, Biava C G, Goodman J R

出版信息

J Pediatr. 1982 Sep;101(3):358-65. doi: 10.1016/s0022-3476(82)80058-9.

Abstract

Lamination of the basement membrane has been considered to be the lesion characteristic of familial nephritis and attenuation to be the lesion of "Benign" familial hematuria. Electron micrographs were reviewed of 57 children who had renal biopsies for persistent hematuria. Attenuation or lamination of the glomerular capillary basement membrane was found in each. Twenty of the 57 children had familial nephritis; 20 had familial hematuria; and 17 had no involved relatives. Follow-up data were available for 14 of 20 children with familial nephritis, 12 of 20 with familial hematuria, and 12 of 17 with sporadic hematuria for 13.6 +/- 6.3, 6.7 +/- 4.6, and 7.0 +/- 4.8 years, respectively, after discovery of hematuria. Five children developed end-stage renal disease: three with familial nephritis, one with familial hematuria, and one with sporadic hematuria. Only two no longer had hematuria. Attenuation of the glomerular capillary basement membrane was seen in every biopsy, whereas lamination was not. Because hematuria and ultrastructural abnormalities were findings shared by all the children, we suggest the possibility that familial nephritis, and familial or sporadic hematuria as defined in this study, may be variations in a spectrum of inherited abnormality or abnormalities in the formation of the glomerular capillary basement membrane.

摘要

基底膜分层一直被认为是家族性肾炎的病变特征,而基底膜变薄则被视为“良性”家族性血尿的病变特征。回顾了57例因持续性血尿而行肾活检的儿童的电子显微镜照片。每例均发现肾小球毛细血管基底膜有变薄或分层现象。57例儿童中,20例有家族性肾炎;20例有家族性血尿;17例无家族史。对20例家族性肾炎患儿中的14例、20例家族性血尿患儿中的12例以及17例散发性血尿患儿中的12例进行了随访,血尿发现后分别随访了13.6±6.3年、6.7±4.6年和7.0±4.8年。5例患儿发展为终末期肾病:3例为家族性肾炎,1例为家族性血尿,1例为散发性血尿。只有2例不再有血尿。每次活检均可见肾小球毛细血管基底膜变薄,而未见分层现象。由于血尿和超微结构异常是所有患儿共有的表现,我们认为家族性肾炎以及本研究中定义的家族性或散发性血尿,可能是肾小球毛细血管基底膜遗传性异常或异常形成谱中的不同表现形式。

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