新闻 自身免疫

抗磷脂抗体的临床意义及抗磷脂综合征的管理

中国 - 2020/04/30

抗磷脂综合征(antiphospholipid syndrome,APS)是一种非炎症性自身免疫病,临床上以动脉、静脉血栓形成,病态妊娠 (妊娠早期流产和中晚期死胎)和血小板减少等症状为表现,血清中存在抗磷脂抗体(antiphospholipid antibody,aPL),上述症状可以单独或多个共同存在,APS 可分为原发性 APS 和继发性 APS,继发性 APS 多见于系统性红斑狼疮(SLE)或类风湿关节炎(RA)等自身免疫病1。

抗磷脂综合征因其临床诊断复杂,患者风险高、预后差,已成为国内外医学领域的共同关注的焦点话题。

划重点

从本周起,沃芬微信公众号将上新自身免疫微信课堂,围绕 APS 的话题展开,由该领域的重量级专家带来。所有视频均录制于去年 10 月在上海举办的“第七届全国生殖免疫高峰论坛”,该论坛由赵爱民教授任大会主席。

本期首先播出日本札幌北海道大学医学院医学教授,风湿病、内分泌和肾脏科主任 Tatsuya Atsumi 主讲的“抗磷脂抗体的临床意义及抗磷脂综合征的管理 ”。敬请关注!

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