Severe Disease Activation after Fingolimod Discontinuation in a Pediatric Multiple Sclerosis Patient: A Case Report and Literature Review.

IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY
Brenda Huppke, Heike de Vries, Astrid Blaschek, Peter Huppke
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引用次数: 0

Abstract

Adult reports of unexpected severe disease worsening, often termed "rebound," shortly after discontinuing fingolimod in a subset of patients with multiple sclerosis (MS), have grown over the last decade. This phenomenon, however, remains poorly described in pediatric MS patients. We present findings of a 15-year-old who experienced a debilitating relapse 4 weeks after stopping fingolimod to switch to ocrelizumab. Imaging revealed multiple large new lesions far exceeding any previously observed activity level in the patient. Despite prompt high-dose corticosteroids, plasma exchange, and prolonged rehabilitation therapy, significant residual deficits involving cognition, balance, and vision remain from the attack. This case underscores that pediatric MS patients are also at risk of severe disease deterioration after fingolimod withdrawal and require close monitoring when switching therapies.

小儿多发性硬化症患者停药后严重疾病激活:1例报告和文献综述。
在过去十年中,关于停止使用芬戈莫德后不久出现意外严重疾病恶化(通常称为“反弹”)的成人报告有所增加。然而,这种现象在儿科患者中仍然很少被描述。我们报告了一名15岁的患者的研究结果,他在停止使用芬戈莫德转而使用奥克雷单抗四周后经历了衰弱性复发。影像学显示多个大的新病灶远远超过任何先前观察到的患者的活动水平。尽管及时给予大剂量皮质类固醇、血浆置换和长期康复治疗,但仍存在严重的认知、平衡和视力缺陷。该病例强调,小儿患者在停药后也有严重疾病恶化的风险,在转换治疗时需要密切监测。
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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来源期刊
Neuropediatrics
Neuropediatrics 医学-临床神经学
CiteScore
2.80
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: For key insights into today''s practice of pediatric neurology, Neuropediatrics is the worldwide journal of choice. Original articles, case reports and panel discussions are the distinctive features of a journal that always keeps abreast of current developments and trends - the reason it has developed into an internationally recognized forum for specialists throughout the world. Pediatricians, neurologists, neurosurgeons, and neurobiologists will find it essential reading.
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