膜性肾病
肾病
医学
计算生物学
病理
肾小球肾炎
内科学
生物
内分泌学
肾
糖尿病
作者
Enrique Dorado,Estefanía Zambrano León,María Victoria García Fernández,Marina Khoury,Silvia Rausch
出处
期刊:PubMed
日期:2024-01-01
卷期号:84 (3): 468-473
摘要
Membranous nephropathy (MN) is the most common cause of primary nephrotic syndrome in adults (20-30%). Light microscopy shows thickening of glomerular basement membrane with appearance of spikes. These histological findings are not evident in early forms, in which case the granular deposition pattern of IgG and/or C3 in the basement membrane by immunofluorescence (IF) constitutes the diagnostic tool that allows to differentiate it from minimal change disease (MCD). Complement system plays a key role in the pathophysiology of MN. C4d is a degradation product and a marker of the complement system activation. C4d labelling by immunohistochemical (HI) technique can help in the differential diagnosis between both glomerulopathies NM and MCD when the material for IF is insufficient and light microscopy is normal. Our objective was to explore the discrimination power of C4d to differentiate between MN and MCD in renal biopsy material.
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