一个原发性膜性肾小球肾炎伴肾病综合征和标准治疗耐药的临床病例

L.D. Denova, I. Krasiuk
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引用次数: 0

摘要

原发性膜性肾小球肾炎的发病率为每年十万分之一(75-80%),男女比例为 2:1。膜性肾小球肾炎的问题在于难以鉴别诊断和经常出现抗药性。10%-20%的患者会出现抗药性,导致终末期肾病,需要进行肾脏替代治疗(透析或肾移植)。我们的研究展示了对一名原发性膜性肾小球肾炎、肾病综合征和标准治疗耐药患者的临床观察结果。在服用利妥昔单抗的背景下,该患者的临床、实验室和仪器指标均呈现出积极的动态变化,生活质量也有所改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A clinical case of primary membranous glomerulonephritis with nephrotic syndrome and resistance to standard treatment
The incidence of primary membranous glomerulonephritis is 1 case per 100,000 each year (75–80 %), with a male-to-female ratio of 2 : 1. It is the cause of idiopathic nephrotic syndrome in more than 20 % of cases (over 40 % in people aged 60 and older). The problem of membranous glomerulonephritis consists in a difficult differential diagnostic search and frequent cases of resistance to treatment. Resistance to treatment may develop in 10–20 % of patients, resulting in the end-stage renal disease requiring renal replacement therapy (dialysis or kidney transplantation). Our work presents the results of clinical observation of a patient with primary membranous glomerulonephritis, nephrotic syndrome and resistance to standard treatment. This patient had a positive dynamics of clinical-laboratory-instrumental indicators and an improvement in the quality of life against the background of taking rituximab.
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