Cheemalavagu Shashank, McCoy Sara S, Knight Jason S
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.
BMJ Case Rep. 2020 Feb 9;13(2):e232907. doi: 10.1136/bcr-2019-232907.
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.
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。