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灾难性抗磷脂综合征1例诊治报告 被引量:1

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摘要 抗磷脂综合征(antiphospholipid syndrome,APS)是自身免疫介导的,以反复动静脉血栓形成、习惯性流产、持续抗磷脂抗体(antiphospholipid antibody,aPL)阳性为特征的一组临床综合征[1]。其中有1%的患者呈现爆发性的多发小血管血栓形成、出现多器官受累的临床表现,称为灾难性抗磷脂综合征(catastrophic antiphospholipid syndrome,CAPS)[2]。
出处 《内科急危重症杂志》 2018年第6期512-515,共4页 Journal of Critical Care In Internal Medicine
基金 国家自然科学基金(No:81501415) 武汉市科技计划项目(No:2017060201010184)
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