原发性膜性肾病-我们今天知道什么?

Marcin Wais, Konrad Warchoł, Adam Jasiura, Aleksandra Wójcik, Kamila Giżewska
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摘要

原发性膜性肾病(PMN)是成人肾病综合征的常见病因,其特征是免疫复合物在肾小球基底膜沉积。本研究目的:评价PMN的发病率、病理、临床特点及免疫抑制治疗的效果。材料和方法:本综述基于PubMed数据库中的文章,关键词“原发性膜性肾病”加上适当的后缀。结果:PMN是一种具有挑战性的疾病,需要多学科的诊断和治疗方法。实验室检查,包括自身抗体和补体水平的评估,对于PMN的诊断是必不可少的。免疫抑制疗法可以有效地诱导相当比例的患者缓解。结论:需要进一步的研究来优化免疫抑制治疗的持续时间和强度,并评估新疗法如利妥昔单抗和贝利单抗的作用。
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Primary Membranous Nephropathy - what do we know today?
Introduction: Primary membranous nephropathy (PMN) is a common cause of nephrotic syndrome in adults, characterized by the deposition of immune complexes in the glomerular basement membrane. Aim of this study: evaluate the features of PMN such as incidence, pathology, clinical features and assess the effectiveness of immunosuppressive therapy. Materials and Methods: The review was based on articles found in PubMed database, using keyword „primary membranous nephropathy” with appropriate sufixes. Results: PMN is a challenging disease that requires a multidisciplinary approach to diagnosis and management. Laboratory tests, including assessment of autoantibodies and complement levels, are essential for the diagnosis of PMN. Immunosuppressive therapy can be effective in inducing remission in a significant proportion of patients. Conclusions: Further research is needed to optimize the duration and intensity of immunosuppressive therapy, and to evaluate the role of newer therapies such as rituximab and belimumab.
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