Langer-Gould Annette, Atlas Scott W, Green Ari J, Bollen Andrew W, Pelletier Daniel
Department of Neurology, Stanford University School of Medicine, Stanford, Calif, USA.
N Engl J Med. 2005 Jul 28;353(4):375-81. doi: 10.1056/NEJMoa051847. Epub 2005 Jun 9.
We describe the clinical course of a patient with multiple sclerosis in whom progressive multifocal leukoencephalopathy (PML), an opportunistic viral infection of the central nervous system, developed during treatment with interferon beta-1a and a selective adhesion-molecule blocker, natalizumab. The first PML lesion apparent on magnetic resonance imaging was indistinguishable from a multiple sclerosis lesion. Despite treatment with corticosteroids, cidofovir, and intravenous immune globulin, PML progressed rapidly, rendering the patient quadriparetic, globally aphasic, and minimally responsive. Three months after natalizumab therapy was discontinued, changes consistent with an immune-reconstitution inflammatory syndrome developed. The patient was treated with systemic cytarabine, and two months later, his condition had improved.
我们描述了一名多发性硬化症患者的临床病程,该患者在接受β-1a干扰素和选择性黏附分子阻滞剂那他珠单抗治疗期间发生了进行性多灶性白质脑病(PML),这是一种中枢神经系统的机会性病毒感染。磁共振成像上出现的首个PML病灶与多发性硬化症病灶难以区分。尽管使用了皮质类固醇、西多福韦和静脉注射免疫球蛋白进行治疗,但PML仍迅速进展,导致患者四肢瘫痪、完全失语且反应极弱。那他珠单抗治疗停药三个月后,出现了与免疫重建炎症综合征相符的变化。该患者接受了全身阿糖胞苷治疗,两个月后病情有所改善。