Hara M, Asada R, Miura I K, Mase D, Inaba S, Higuchi A, Tanizawa T, Sado Y, Okada T
Am J Clin Pathol. 1986 Dec;86(6):792-7. doi: 10.1093/ajcp/86.6.792.
In this report, the authors describe a case of a 2-year, 11-month-old girl with glomerulonephritis and no family history of renal diseases and deafness. Immunofluorescent studies in the renal biopsy specimens with the use of anti-sera against human glomerular basement membrane (GBM) and P3 antigen (prepared from bovine GBM and inducible of Steblay's type nephritis in rats) demonstrated focal and segmental distribution of the GBM antigen(s). Electron microscopic examination revealed splitting and thinning of the GBM. Indirect immunofluorescence showed that there was no binding of Goodpasture's anti-GBM antibodies to the glomeruli. These findings are similar to those in patients with hereditary nephritis. The immunofluorescent examination of the fixation of the various anti-sera, including anti-types IV and V collagens, laminin, fibronectin, and actomyosin sera on the GBM, revealed normal reactivity. The abnormalities observed in this case may be a part of the spectrum of primary GBM defects.
在本报告中,作者描述了一例2岁11个月大的女孩,患有肾小球肾炎,且无肾脏疾病和耳聋的家族病史。在肾脏活检标本中,使用抗人肾小球基底膜(GBM)和P3抗原(由牛GBM制备,可在大鼠中诱导出Steblay型肾炎)的抗血清进行免疫荧光研究,结果显示GBM抗原呈局灶性和节段性分布。电子显微镜检查显示GBM出现分裂和变薄。间接免疫荧光显示,Goodpasture抗GBM抗体与肾小球无结合。这些发现与遗传性肾炎患者的发现相似。对包括抗IV型和V型胶原、层粘连蛋白、纤连蛋白和肌动球蛋白血清在内的各种抗血清在GBM上的固定情况进行免疫荧光检查,结果显示反应正常。该病例中观察到的异常情况可能是原发性GBM缺陷谱系的一部分。