原发性局灶节段性肾小球硬化:为什么这个谜团仍然缺失?

H. Trimarchi
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引用次数: 2

摘要

局灶节段性肾小球硬化(FSGS)可分为原发性和继发性。此外,近年来已经确定了许多原发性FSGS的原因。在这方面,遗传循环通透性因子和共刺激分子的足细胞异常表达已被报道。然而,这种实体的分类仍然难以理解,主要是因为它描述了疤痕的形态模式。FSGS是几乎所有肾小球肾炎共有的一种组织学模式,它描述的是足细胞病变,而不是疾病。因此,应根据新的病理生理发现和每个触发通路中遇到的生物标志物进行重新分类。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Focal Segmental Glomerulosclerosis: Why Are Pieces of This Puzzle Still Missing?
Focal segmental glomerulosclerosis (FSGS) can be classified as primary or secondary. Moreover, many causes of primary FSGS have been identified in recent years. In this regard, genetic circulating permeability factors and the abnormal podocyte expression of co-stimulatory molecules have been reported. However, the classification of this entity remains difficult to understand, mainly due to the fact that it describes a morphologic pattern of scarring. FSGS is a histological pattern shared by almost all the glomerulonephritides that describes a podocyte lesion and not a disease. Therefore, it should be reclassified according to the new pathophysiological findings and the biomarkers encountered in each triggered pathway.
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