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阿达木单抗诱导的抗磷脂综合征继发的手指缺血

Digital ischaemia secondary to adalimumab-induced antiphospholipid syndrome.

作者信息

Cheemalavagu Shashank, McCoy Sara S, Knight Jason S

机构信息

Internal Medicine, University of Michigan Hospital, Ann Arbor, Michigan, USA.

Division of Rheumatology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

出版信息

BMJ Case Rep. 2020 Feb 9;13(2):e232907. doi: 10.1136/bcr-2019-232907.

Abstract

A 50-year-old woman with a history of Crohn's disease treated with adalimumab presented with left hand pain and duskiness. Angiogram showed non-filling of the radial and digital arteries of the hand. Antiphospholipid antibody testing was positive, leading to a diagnosis of antitumour necrosis factor-induced antiphospholipid syndrome. Adalimumab was discontinued, and she was treated with the vitamin K antagonist warfarin and low-dose aspirin. Upon resolution of the antiphospholipid antibodies, she was transitioned to aspirin alone without recurrence of thrombosis.

摘要

一名50岁有克罗恩病病史且接受阿达木单抗治疗的女性,出现左手疼痛和皮肤发暗。血管造影显示手部桡动脉和指动脉未显影。抗磷脂抗体检测呈阳性,导致诊断为抗肿瘤坏死因子诱导的抗磷脂综合征。停用阿达木单抗,她接受了维生素K拮抗剂华法林和低剂量阿司匹林治疗。抗磷脂抗体消退后,她仅改用阿司匹林治疗,血栓未复发。

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