0 UROLOGY & NEPHROLOGY
Mariela Navarro-Torres, Benjamin Wooden, Dominick Santoriello, Jai Radhakrishnan, Andrew S. Bomback
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引用次数: 0

摘要

足细胞是肾小球滤过屏障的重要组成部分。对这些特化细胞的损伤导致足细胞病。肾活检可发现局灶节段性肾小球硬化或微小病变。这些疾病可能具有不同的临床表现和活检特征,这将有助于将其分为原发性或继发性足细胞病变,并进一步指导治疗。与继发性局灶节段性肾小球硬化相反,原发性局灶节段性肾小球硬化和微小改变疾病需要免疫抑制,因为自发缓解很少,与肾病综合征相关的并发症可能危及生命。继发于基因突变的足细胞病很少需要免疫抑制,但这可能在特殊人群中表明。本文就足细胞病的诊断和治疗要点进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Podocytopathies
The podocyte is a critical component of the glomerular filtration barrier. Injury to these specialized cells results in podocytopathies. A kidney biopsy will reveal focal segmental glomerulosclerosis or minimal change disease. These diseases can have variable clinical presentations and biopsy features, which will help classify them into primary or secondary podocytopathies and further guide treatment. Contrary to secondary focal segmental glomerulosclerosis, primary focal segmental glomerulosclerosis and minimal change disease require immunosuppression since spontaneous remission is rare and complications related to nephrotic syndrome can be life-threatening. Podocytopathies secondary to genetic mutations rarely require immunosuppression, but this may be indicated in special populations. The purpose of this review is to discuss key points in diagnosis and treatment for patients with podocytopathies.
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CiteScore
5.30
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0.00%
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