Adalimumab-Induced Thrombocytopenia: A Case Report of Drug-Induced Thrombocytopenia.

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2025-09-08 eCollection Date: 2025-01-01 DOI:10.1155/crh/4414589
Shelby E Jones, Joshua Sellers, Margaret C Wheless, Danielle Fishman, Robert K McKenzie
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引用次数: 0

Abstract

In this case report, we present a patient with severe thrombocytopenia induced by adalimumab after 4 weeks of treatment for rheumatoid arthritis. This case adds to present literature regarding antitumor necrosis factor-alpha (TNF-α)-induced thrombocytopenia and explores the use of thrombopoietin receptor agonist medications in refractory drug-induced immune thrombocytopenia (DITP). A 57-year-old female with a history of rheumatoid arthritis presented to the emergency department for progressive petechial rash 4 days after her third dose of adalimumab. It was determined that the patient had immune thrombocytopenia caused by adalimumab and was initially treated with steroids and intravenous immunoglobulin (IVIG). Platelets remained undetectable; hence, romiplostim was initiated, after which platelets trended up to normal levels a week later. Anti-TNF-α agents carry the risk of severe side effects, including thrombocytopenia, which should be monitored closely in the first few months of therapy. The treatment of DITP is challenging, especially when the causative agent has a prolonged half-life.

阿达木单抗致血小板减少1例。
在这个病例报告中,我们提出了一个患者严重的血小板减少症由阿达木单抗治疗4周后,类风湿关节炎。本病例补充了目前关于抗肿瘤坏死因子-α (TNF-α)诱导的血小板减少的文献,并探讨了血小板生成素受体激动剂在难治性药物诱导的免疫性血小板减少(DITP)中的应用。一名57岁女性,有类风湿关节炎病史,在第三次阿达木单抗治疗4天后因进行性点疹就诊于急诊科。确定患者有阿达木单抗引起的免疫性血小板减少症,最初使用类固醇和静脉注射免疫球蛋白(IVIG)治疗。血小板仍未检测到;因此,开始使用romiplostim,一周后血小板趋于正常水平。抗tnf -α药物具有严重副作用的风险,包括血小板减少症,在治疗的前几个月应密切监测。DITP的治疗具有挑战性,特别是当病原体的半衰期延长时。
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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审稿时长
13 weeks
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