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度普利尤单抗用于咽鼓管功能障碍后发生的急性重症免疫性血小板减少症:一例报告

Acute Severe Immune Thrombocytopenia Following Dupilumab Use for Eustachian Tube Dysfunction: A Case Report.

作者信息

Lu Amanda J, Morris Sean, Weissmann Lisa

机构信息

Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, USA.

Medicine, Mount Auburn Hospital, Harvard Medical School, Cambridge, USA.

出版信息

Cureus. 2025 Jul 11;17(7):e87724. doi: 10.7759/cureus.87724. eCollection 2025 Jul.

Abstract

Immune thrombocytopenic purpura (ITP) is a rare hematologic disorder characterized by isolated thrombocytopenia and mucocutaneous bleeding. While drug-induced ITP (DITP) is recognized with certain medications, reports associated with dupilumab, a monoclonal antibody used for atopic dermatitis and other inflammatory conditions, are exceedingly rare. We present a case of acute, severe thrombocytopenia occurring two weeks after dupilumab initiation for eustachian tube dysfunction in a 76-year-old male. Comprehensive evaluation excluded secondary causes, supporting a diagnosis of dupilumab-induced ITP. Treatment with corticosteroids and intravenous immunoglobulin led to rapid platelet recovery. Given the expanding use of dupilumab, awareness of this rare but potentially serious adverse event is crucial. Clinicians should remain vigilant for mucocutaneous bleeding in patients receiving biologic agents and initiate appropriate treatment promptly. Moreover, enhanced pharmacovigilance and further research are needed to elucidate the incidence, risk factors, and mechanisms of dupilumab-associated hematologic toxicity.

摘要

免疫性血小板减少性紫癜(ITP)是一种罕见的血液系统疾病,其特征为孤立性血小板减少和皮肤黏膜出血。虽然药物性ITP(DITP)与某些药物有关,但与用于特应性皮炎和其他炎症性疾病的单克隆抗体度普利尤单抗相关的报告极为罕见。我们报告一例76岁男性因咽鼓管功能障碍开始使用度普利尤单抗两周后发生急性、严重血小板减少的病例。全面评估排除了继发原因,支持度普利尤单抗诱导的ITP诊断。使用皮质类固醇和静脉注射免疫球蛋白治疗后血小板迅速恢复。鉴于度普利尤单抗的使用不断增加,认识到这种罕见但可能严重的不良事件至关重要。临床医生应对接受生物制剂治疗的患者的皮肤黏膜出血保持警惕,并及时启动适当治疗。此外,需要加强药物警戒并进行进一步研究,以阐明度普利尤单抗相关血液毒性的发生率、危险因素和机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cb7/12335817/b103607c78a7/cureus-0017-00000087724-i01.jpg

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