Jander Sebastian, Turowski Bernd, Kieseier Bernd C, Hartung Hans-Peter
Department of Neurology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.
Mult Scler. 2012 Nov;18(11):1650-2. doi: 10.1177/1352458512463768.
In this report we describe a multiple sclerosis patient who developed a relapse with magnetic resonance imaging (MRI) features of tumefactive demyelination after switching therapy from natalizumab to fingolimod. Tumefactive lesions emerged 16 weeks after stopping natalizumab and eight weeks after commencing fingolimod therapy but had been absent at the time of diagnosis and throughout the preceding course of the disease. Thus, the first-time occurrence of atypical lesion features may have been caused by the change in immunotherapy. The possible relevance of natalizumab withdrawal vs fingolimod introduction is discussed against the background of recently published case studies.
在本报告中,我们描述了一名多发性硬化症患者,该患者在从那他珠单抗转换为芬戈莫德治疗后出现了具有肿胀性脱髓鞘磁共振成像(MRI)特征的病情复发。肿胀性病变在停用那他珠单抗16周后以及开始使用芬戈莫德治疗8周后出现,但在诊断时及整个疾病前期病程中均未出现。因此,非典型病变特征的首次出现可能是由免疫治疗的改变所致。结合最近发表的病例研究背景,讨论了停用那他珠单抗与引入芬戈莫德的可能相关性。