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先天性梅毒与具有免疫发病机制证据的肾小球肾炎。

Congenital syphilis and glomerulonephritis with evidence for immune pathogenesis.

作者信息

Wiggelinkhuizen J, Kaschula R O, Uys C J, Kuijten R H, Dale J

出版信息

Arch Dis Child. 1973 May;48(5):375-81. doi: 10.1136/adc.48.5.375.

Abstract

In 3 infants with congenital syphilis the dominant clinical manifestation of syphilitic kidney disease was the nephrotic syndrome. Mesangioendothelial proliferation was present in 2 cases and mixed proliferative glomerulonephritis with crescent formation in the third. The severity of the clinical and histopathological abnormalities could be related to the apparent duration of the illness. In all 3 cases immune complex deposition could be shown within and along the epithelial aspect of the glomerular basement membrane on light, electron, and immunofluorescent microscopy. These features, together with a reduced total serum haemolytic complement, suggest an immune pathogenesis of the glomerulonephritis associated with early congenital syphilis.

摘要

在3例先天性梅毒患儿中,梅毒性肾病的主要临床表现为肾病综合征。2例出现系膜内皮细胞增生,第3例为伴有新月体形成的混合性增生性肾小球肾炎。临床和组织病理学异常的严重程度可能与疾病的明显病程有关。在所有3例病例中,光镜、电镜和免疫荧光显微镜检查均显示免疫复合物在肾小球基底膜上皮侧及内部沉积。这些特征,再加上血清总溶血补体降低,提示与早期先天性梅毒相关的肾小球肾炎存在免疫发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7980/1648370/76ae616aac92/archdisch00865-0050-a.jpg

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