Dorado Enrique G, Zambrano León Estefanía, García Fernández María Victoria, Khoury Marina, Rausch Silvia
Departamento de Nefrología, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, Buenos Aires, Argentina. E-mail:
Departamento de Nefrología, Instituto de Investigaciones Médicas Alfredo Lanari, Universidad de Buenos Aires, Buenos Aires, Argentina.
Medicina (B Aires). 2024;84(3):468-473.
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.
Paraffin-embedded samples were recovered from renal biopsies with a diagnosis of MN and MCD performed between 1/1/2008 and 4/1/2019. IH staining was performed by immunoperoxidase technique using a rabbit anti-human C4d polyclonal antibody.
In all cases with MN (n = 27, 15 males) with a median age of 63 (range: 18-87) years, C4d deposits were detected. In 21 cases with MCD (12 males) with a median age of 51 (range: 18-87) years, the C4d marking was negative in every samples.
The results indicate that the marking of the renal biopsy with C4d is a useful tool for the differential diagnosis between NM and MCD.
膜性肾病(MN)是成人原发性肾病综合征最常见的病因(20%-30%)。光镜下可见肾小球基底膜增厚并出现钉突。这些组织学表现在早期并不明显,在这种情况下,免疫荧光(IF)显示基底膜中IgG和/或C3的颗粒状沉积模式是将其与微小病变肾病(MCD)区分开来的诊断工具。补体系统在MN的病理生理学中起关键作用。C4d是补体系统激活的降解产物和标志物。当IF材料不足且光镜正常时,免疫组织化学(HI)技术检测C4d标记有助于NM和MCD这两种肾小球病的鉴别诊断。我们的目的是探讨C4d在肾活检材料中区分MN和MCD的鉴别能力。
从2008年1月1日至2019年4月1日期间诊断为MN和MCD的肾活检石蜡包埋样本中获取样本。使用兔抗人C4d多克隆抗体通过免疫过氧化物酶技术进行IH染色。
在所有MN病例(n = 27,15名男性)中,中位年龄为63岁(范围:18-87岁),均检测到C4d沉积。在21例MCD病例(12名男性)中,中位年龄为51岁(范围:18-87岁),每个样本的C4d标记均为阴性。
结果表明,肾活检C4d标记是NM和MCD鉴别诊断的有用工具。