Primary antiphospholipid syndrome in the elderly: Four strokes and mechanical thrombectomies until the diagnosis - A case report.

IF 2.3 4区 医学 Q3 CLINICAL NEUROLOGY
Brain Circulation Pub Date : 2024-06-26 eCollection Date: 2024-04-01 DOI:10.4103/bc.bc_67_23
Anatoli Anastasiadi, Chiara Bott, Daniel Kitterer, Elke Roser, Hans Henkes, Hansjörg Bäzner, Marc E Wolf
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引用次数: 0

Abstract

Antiphospholipid syndrome (APS) is known as a rare etiology of embolic ischemic stroke. In individuals below 50 years, up to 20% of strokes are associated with APS, whereas in patients >50 years, it is considered a very seldom cause of stroke. We describe the course of a 66-year-old white woman, who experienced four embolic strokes with large vessel occlusion over a period of 2 years, which were repeatedly and successfully treated by mechanical thrombectomy. Initially attributed to atrial fibrillation and treated with direct oral anticoagulants, the patient was finally diagnosed with primary APS due to isolated anti-beta 2-glycoprotein antibodies and successfully treated after several stroke recurrences. After initiation of Vitamin K antagonist therapy, no further strokes occurred. For recurrent embolic stroke despite oral anticoagulation, late-onset APS might be considered a rare etiology also in the elderly.

老年人原发性抗磷脂综合征:直到确诊前的四次中风和机械性血栓切除术--病例报告。
众所周知,抗磷脂综合征(APS)是栓塞性缺血性脑卒中的一种罕见病因。在 50 岁以下的人群中,多达 20% 的中风与 APS 有关,而在 50 岁以上的患者中,APS 被认为是极少见的中风病因。我们描述了一位 66 岁白人女性的病程,她在 2 年内经历了 4 次伴有大血管闭塞的栓塞性脑卒中,并多次通过机械性血栓切除术成功治疗。患者最初被诊断为心房颤动,并接受了直接口服抗凝剂治疗,但最终被诊断为原发性 APS,原因是分离出了抗 beta 2-糖蛋白抗体,并在数次中风复发后成功接受了治疗。在开始接受维生素 K 拮抗剂治疗后,没有再发生中风。对于口服抗凝药后仍复发的栓塞性中风,晚发型 APS 可能被认为是一种罕见的病因,在老年人中也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brain Circulation
Brain Circulation Multiple-
自引率
5.30%
发文量
31
审稿时长
16 weeks
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