原发性抗磷脂综合征的膜性肾病

Clinical Kidney Journal Pub Date : 2024-02-01 DOI:10.1093/ckj/sfae017

R. Stammler, Camille Rapoport, Jean-Paul Duong Van Huyen, Stéphane Zuily, Olivier Moranne, Eric Daugas, Emmanuel Esteve, Mathilde de Menthon, Hélène Perrochia, Charlotte Mussini, Aurélie Sannier, Marion Rabant, David Buob, Alexandre Karras

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引用次数: 0

摘要

抗磷脂综合征（APS）是一种全身性自身免疫性疾病，其特征是与抗磷脂抗体相关的血栓和产科并发症。APS 的肾脏受累范围包括多种类型的肾病，主要是血管性肾病[......]。

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Membranous nephropathy in primary antiphospholipid syndrome

Antiphospholipid syndrome ( APS) is a systemic autoimmune disorder characterized by thrombotic and obstetrical complications associated with antiphospholipid antibodies. The spectrum of renal involvement in APS comprises several types of nephropathy, mainly vascular nephropathies [

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Clinical Kidney Journal

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