梅奥诊所关于膜性肾病的共识报告;向更好地治疗疾病迈出了充满希望的一步

Q3 Medicine
S. Zandifar, Leila Alem, Azadeh Khayyat, Mohammad Ali Esmaeil pour
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引用次数: 0

摘要

膜性肾病是一种由上皮下沉积物引起的免疫复合物疾病。膜性肾病的病理表现是肾小球基底膜上皮细胞内产生免疫复合物。原发性膜性肾病的既定病理特征包括上皮下免疫沉积、肾小球基底膜增厚和荚膜脚突起脱落。原发性膜性肾病病理特征的临床意义包括男性性别、年龄、持续大量蛋白尿、发病时肾小球滤过率下降和肾小管间质纤维化。膜性肾病是通过肾活检确诊的,活检可确认上皮下免疫沉积、肾小球基底膜增厚和荚膜足突脱落。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Mayo Clinic consensus report on membranous nephropathy; a promising step toward better treating the disease
Membranous nephropathy is an immune complex disease caused by subepithelial deposits. The pathological manifestations of membranous nephropathy are considered by the creation of immune complexes in the epithelial cells of the glomerular basement membrane. The established pathologic features of primary membranous nephropathy include subepithelial immune deposits, thickening of the glomerular basement membrane, and podocyte foot process effacement. The clinical implications of pathological features of primary membranous nephropathy include male gender, age, persistent heavy proteinuria, decreased glomerular filtration rate on presentation, and tubulointerstitial fibrosis. Membranous nephropathy is diagnosed through a kidney biopsy, confirming subepithelial immune deposits, thickening of the glomerular basement membrane, and podocyte foot process effacement.
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来源期刊
Journal of Nephropharmacology
Journal of Nephropharmacology Medicine-Pharmacology (medical)
CiteScore
1.70
自引率
0.00%
发文量
18
审稿时长
4 weeks
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