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[阿哌沙班治疗下的高危型静脉抗磷脂综合征患者的Libman-Sacks心内膜炎]

[Libman-Sacks endocarditis under apixaban in a patient with a high-risk profile venous antiphospholipid syndrome].

作者信息

Allain J-S, Paven E, Henriot B, Belhomme N, Le Bot A, Ballerie A, Jego P

机构信息

Department of Internal Medicine and Clinical Immunology, Unité d'Investigation Clinique, Rennes University Hospital, Pontchaillou Hospital, 2, rue Henri-Le-Guilloux, 35 000 Rennes, France; Pole CVM, Paul Broussais General Hospital Center, Saint Malo, France; Clinical Investigation Center of Rennes, National Institute of Health and Scientific Research (CIC-INSERM 1414), Rennes, France.

Department of Cardiology, Rennes University Hospital, Pontchaillou Hospital, Rennes, France.

出版信息

Rev Med Interne. 2021 Mar;42(3):218-222. doi: 10.1016/j.revmed.2020.08.009. Epub 2020 Nov 3.

Abstract

INTRODUCTION

Libman-Sacks endocarditis is a rare complication of antiphospholipid syndrome. Anti-vitamin K therapy is the standard treatment, although valvular replacement surgery may be required in some severe cases. In the latest EULAR recommendations, it is advised not to use direct oral anticoagulants in the management of antiphospholipid syndrome, especially of high-risk profile.

CASE REPORT

We present a case of a mitral Libman-Sacks endocarditis complicated with multiple strokes occurring in the setting of an antiphospholipid syndrome with triple positive antibody profile in a 63-year-old woman with multiple sclerosis. She was previously treated with apixaban for two years. Tinzaparin followed by prolonged warfarine treatment and two months of hydroxychloroquine resulted in valvular improvement.

CONCLUSION

To our knowledge, this is the first case of Libman-Sacks endocarditis occurring during apixaban therapy in a patient with antiphospholipid syndrome. This severe case highlights the inefficiency of direct oral anticoagulants to prevent thrombotic events in the antiphospholipid syndrome.

摘要

引言

利布曼-萨克斯心内膜炎是抗磷脂综合征的一种罕见并发症。抗维生素K治疗是标准疗法,不过在一些严重病例中可能需要进行瓣膜置换手术。在欧洲抗风湿病联盟(EULAR)的最新建议中,建议在抗磷脂综合征的管理中,尤其是高危型患者,不要使用直接口服抗凝剂。

病例报告

我们报告一例63岁患有多发性硬化症的女性,其患有抗磷脂综合征且抗体三项呈阳性,并发二尖瓣利布曼-萨克斯心内膜炎及多次中风。她此前接受阿哌沙班治疗两年。之后使用替奈肝素,接着长期服用华法林并使用两个月的羟氯喹,瓣膜状况得到改善。

结论

据我们所知,这是抗磷脂综合征患者在接受阿哌沙班治疗期间发生利布曼-萨克斯心内膜炎的首例病例。这一严重病例凸显了直接口服抗凝剂在预防抗磷脂综合征血栓形成事件方面的无效性。

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