地纽昔单抗诱发非典型溶血性尿毒症病例报告

IF 0.9 4区 医学 Q4 HEMATOLOGY
Letha Huang, Danielle Miller, Fouad Hajjar
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引用次数: 0

摘要

描述非典型溶血性尿毒症(aHUS)的发生与使用地纽昔单抗之间关系的证据有限。本病例报告描述了一名患有神经母细胞瘤的 20 岁男性患者在使用地纽昔单抗后出现非典型溶血性尿毒症。患者出现无法控制的高血压和肾功能障碍,最终通过肾活检明确诊断为 aHUS。患者需要使用依库珠单抗进行补体引导治疗,后来转为使用雷珠单抗。本病例进一步描述了地努昔单抗用药与 aHUS 发展之间的先后关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Case Report of Dinutuximab-induced Atypical Hemolytic Uremic Syndrome.

Limited evidence exists describing the relationship between the development of atypical hemolytic uremic syndrome (aHUS) and the administration of dinutuximab. This case report describes a 20-year-old male with neuroblastoma who experienced aHUS post-dinutuximab administration. The patient presented with uncontrolled hypertension and renal dysfunction, ultimately receiving a definitive diagnosis of aHUS through a renal biopsy. The patient required complement-directed therapy with eculizmab and later transitioned to ravulizumab. This case further describes a sequential relationship between dinutuximab administration and aHUS development.

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来源期刊
CiteScore
1.90
自引率
8.30%
发文量
415
审稿时长
2.5 months
期刊介绍: ​Journal of Pediatric Hematology/Oncology (JPHO) reports on major advances in the diagnosis and treatment of cancer and blood diseases in children. The journal publishes original research, commentaries, historical insights, and clinical and laboratory observations.
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