以反复肺动脉栓塞为首发症状的原发性抗磷脂综合征1例  

A case of primary antiphospholipid syndrome with recurrent pulmonary embolism as the first symptom

作　　者：张金 李程 张如意 韩笑蓉 陈中波 王英慧 孙健[1] ZHANG Jin;LI Cheng;ZHANG Ruyi;HAN Xiaorong;CHEN Zhongbo;WANG Yinghui;SUN Jian(Department of Cardiology,the First Hospital of Jilin University,Changchun,130000,China)

机构地区：[1]吉林大学第一医院心内科,长春130000

出　　处：《临床心血管病杂志》2020年第7期684-686,共3页Journal of Clinical Cardiology

摘　　要：抗磷脂综合征(antiphospholipid syndrome,APS)是一种自身免疫状态,可以针对某些磷脂结合的血浆蛋白产生自身抗体,与血栓形成(包括静脉和动脉)、妊娠丢失等疾病发生风险相关。发生在没有其他自身免疫性疾病的情况下,称为原发性APS(primary APS,PAPS)。发生在系统性红斑狼疮或其他自身免疫性疾病患者的APS被称为继发性APS(secondary APS,SAPS)。APS特征是血液循环中抗磷脂抗体(antiphospholipid antibodies,APL)持续阳性.Extensive pulmonary disease may occur in antiphospholipid syndrome.The most common pulmonary manifestation is pulmonary thromboembolism.Therefore,for patients with pulmonary embolism,we should pay special attention to the possibility of autoimmune diseases,in order to early diagnosis and treatment.

关 键 词：肺栓塞 抗磷脂综合征 

分 类 号：R593.2[医药卫生—内科学]