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伴有主要动脉血栓形成的抗磷脂综合征，表现为肺血栓栓塞、脑血管意外和冠状动脉疾病：一例报告及文献综述

Antiphospholipid syndrome with major arterial thrombosis, presenting as pulmonary thromboembolism, cerebrovascular accident, and coronary artery disease: A case report and literature review.

作者信息

Shirani Aria, Daraei Morteza, Shirani Aryan

机构信息

Research Scholar, School of Medicine Iran University of Medical Sciences Tehran Iran.

Assistant Professor of Internal Medicine, Department of Internal Medicine Imam Khomeini Hospital Complex Tehran Iran.

出版信息

Clin Case Rep. 2024 Aug 5;12(8):e9254. doi: 10.1002/ccr3.9254. eCollection 2024 Aug.

DOI:10.1002/ccr3.9254
PMID:39104736
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11299070/
Abstract

Antiphospholipid syndrome is an immunopathologic disorder that should be considered in all patients with recurrent and/or unexplained thromboembolic events. Antiphospholipid antibodies are diagnostic markers, and anticoagulation therapy is the therapeutic and preventive strategy. Long-term anticoagulation therapy is necessary, with careful attention to potential bleeding complications.

摘要

抗磷脂综合征是一种免疫病理疾病，所有复发性和/或不明原因血栓栓塞事件的患者均应考虑此病。抗磷脂抗体是诊断标志物，抗凝治疗是治疗和预防策略。长期抗凝治疗是必要的，同时要密切关注潜在的出血并发症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efa/11299070/76f7c48ddafa/CCR3-12-e9254-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efa/11299070/abeed8437eac/CCR3-12-e9254-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efa/11299070/76f7c48ddafa/CCR3-12-e9254-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efa/11299070/abeed8437eac/CCR3-12-e9254-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7efa/11299070/76f7c48ddafa/CCR3-12-e9254-g001.jpg

相似文献

1
Antiphospholipid syndrome with major arterial thrombosis, presenting as pulmonary thromboembolism, cerebrovascular accident, and coronary artery disease: A case report and literature review.伴有主要动脉血栓形成的抗磷脂综合征，表现为肺血栓栓塞、脑血管意外和冠状动脉疾病：一例报告及文献综述
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本文引用的文献

1
Epidemiology of antiphospholipid syndrome: macro- and microvascular manifestations.抗磷脂综合征的流行病学：大血管和微血管表现。
Rheumatology (Oxford). 2024 Feb 6;63(SI):SI24-SI36. doi: 10.1093/rheumatology/kead571.
2
Global Antiphospholipid Syndrome Score (GAPSS) in Patients with Systemic Lupus Erythematosus.系统性红斑狼疮患者的全球抗磷脂抗体综合征评分（GAPSS）。
Dokl Biochem Biophys. 2023 Aug;511(1):227-234. doi: 10.1134/S160767292370028X. Epub 2023 Oct 13.
3
2023 ACR/EULAR antiphospholipid syndrome classification criteria.
2023 年 ACR/EULAR 抗磷脂综合征分类标准。
Ann Rheum Dis. 2023 Oct;82(10):1258-1270. doi: 10.1136/ard-2023-224609. Epub 2023 Aug 28.
4
Antiphospholipid syndrome: advances in diagnosis, pathogenesis, and management.抗磷脂综合征：诊断、发病机制及管理方面的进展
BMJ. 2023 Feb 27;380:e069717. doi: 10.1136/bmj-2021-069717.
5
A Case Report of Anti-phospholipid Syndrome With Lower Extremity Arterial Thrombosis That Didn't Respond to Heparin and Direct Oral Anticoagulation: Ultimately, the Patient Agreed to Oral Warfarin.1例抗磷脂综合征合并下肢动脉血栓形成患者对肝素和直接口服抗凝药治疗无效：最终，患者同意口服华法林。
Cureus. 2022 Nov 8;14(11):e31230. doi: 10.7759/cureus.31230. eCollection 2022 Nov.
6
Bilateral Upper Limb Symmetrical Digital Gangrene: A Rare Presentation of Anti-Phospholipid Syndrome.双侧上肢对称性指端坏疽：抗磷脂综合征的一种罕见表现
Cureus. 2022 Sep 23;14(9):e29516. doi: 10.7759/cureus.29516. eCollection 2022 Sep.
7
Direct oral anticoagulants versus warfarin in patients with antiphospholipid syndrome: A meta-analysis of randomized controlled trials.直接口服抗凝剂与华法林用于抗磷脂综合征患者的疗效比较：一项随机对照试验的荟萃分析
Lupus. 2022 Oct;31(11):1335-1343. doi: 10.1177/09612033221118463. Epub 2022 Aug 13.
8
Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.凝血酶原G20210A基因突变所致复发性深静脉血栓形成和肺栓塞：病例报告及文献复习
J Investig Med High Impact Case Rep. 2022 Jan-Dec;10:23247096211058486. doi: 10.1177/23247096211058486.
9
Polycythemia vera presenting with pulmonary embolism and splenic infarction: a case report.真性红细胞增多症合并肺栓塞和脾梗死 1 例报告。
J Int Med Res. 2022 Jan;50(1):3000605211072801. doi: 10.1177/03000605211072801.
10
Epidemiology of Antiphospholipid Syndrome in the General Population.抗磷脂综合征在普通人群中的流行病学。
Curr Rheumatol Rep. 2022 Jan 5;23(12):85. doi: 10.1007/s11926-021-01038-2.