1例原发性抗磷脂综合征和冠状病毒病的斯坦福A型主动脉夹层

Q3 Medicine
AORTA Pub Date : 2023-02-01 DOI:10.1055/s-0042-1757952
Sarah A Ahmad, Nauman Khalid, Lovely Chhabra, Waleed T Kayani, Tarek Helmy
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引用次数: 0

摘要

急性主动脉夹层是最致命的疾病之一,它影响了主动脉壁的内壁。我们描述了一例斯坦福a型主动脉夹层患者,该患者患有原发性抗磷脂综合征(APS)并合并2019年冠状病毒病(COVID-19)。APS的特征是静脉和/或动脉血栓形成,血小板减少,很少出现血管动脉瘤。APS引起的高凝环境和COVID-19引起的血栓形成前状态对患者实现最佳术后抗凝提出了挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Stanford Type A Aortic Dissection in A Patient with Primary Antiphospholipid Syndrome and Coronavirus Disease 2019.

Stanford Type A Aortic Dissection in A Patient with Primary Antiphospholipid Syndrome and Coronavirus Disease 2019.

Acute aortic dissection is one of the most lethal diseases, affecting the lining of the aortic wall. We describe a case of Stanford Type A aortic dissection in a patient with underlying primary antiphospholipid syndrome (APS) complicated by coronavirus disease 2019 (COVID-19). APS is characterized by recurrent venous and/or arterial thrombosis, thrombocytopenia, and rarely vascular aneurysms. The hypercoagulable milieu attributable to APS and the prothrombotic state from COVID-19 posed a challenge in achieving optimal postoperative anticoagulation in our patient.

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来源期刊
AORTA
AORTA Medicine-Surgery
CiteScore
1.00
自引率
0.00%
发文量
119
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