一名重症抗磷脂综合征患者的恶性复发性血栓形成及其 30 天后的结果

IF 2.1 Q4 IMMUNOLOGY
Immuno Pub Date : 2024-03-04 DOI:10.3390/immuno4010008
P. Di Micco, Maurizio Dorato, Maurizio Latte, Maria D’Antò, Vittorio Luiso, Gerolamo Sibilio
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引用次数: 0

摘要

灾难性抗磷脂综合征(CAPS)是抗磷脂综合征(APS)的一种罕见临床形式,由于可能同时影响大、小血管的血栓形成而导致危及生命的并发症。它可能同时发生在静脉和/或动脉,目前还没有基于随机临床试验或大型系列研究的指南。我们在此报告了一例临床病例,该病例在无症状感染 SARS-CoV-2 后发病,尽管在标签外使用低剂量低分子量肝素治疗,但血栓复发后使用华法林治疗后病情得到短暂改善。此外,由于该病发病率高、死亡率高、住院时间长,我们试图找出一条多学科团队可据以设定具体随访时间的路线。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fulminant Recurrent Thrombosis in a Patient with Catastrophic Antiphospholipid Syndrome and Its Thirty-Day Outcome
Catastrophic antiphospholipid syndrome (CAPS) is a rare clinical form of antiphospholipid syndrome (APS) associated with life-threatening complications due to simultaneous thrombosis that may affect small and large vessels. It may be localized to the venous and/or arteries at the same time, and there are not available guidelines based on randomized clinical trials or large series. We here report a clinical case of CAPS with onset after resolution of oligo-symptomatic infection SARS-CoV-2, that had transient improvement with warfarin after recurrent thromboses occurred despite treatment off-label with low doses of low molecular weight heparin. Furthermore, we tried to trace a line by which a multidisciplinary team may set specific timing to have follow-up because of the high morbidity, mortality, and prolonged time of hospitalization.
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CiteScore
2.60
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