作者: Laura E. Baldassari , Stephen E. Jones , David B. Clifford , Robert J. Fox
DOI: 10.1212/CPJ.0000000000000457
关键词: Pediatrics 、 Natalizumab 、 Medicine 、 White matter 、 Medical history 、 Progressive multifocal leukoencephalopathy 、 CHOP 、 Multiple sclerosis 、 Expressive aphasia 、 Hyperintensity
摘要: A 53-year-old man with an 18-year history of multiple sclerosis (MS) was treated natalizumab for 7 years. Two years prior to presentation, treatment interval increased every 6 weeks in attempt reduce the risk PML. Medical notable cutaneous T-cell lymphoma status-post CHOP chemotherapy. JCV serology positive (index 2.8). He presented our tertiary referral center consultation due 8 months progressive left-sided paresthesias, 4 right arm clumsiness, and several expressive aphasia. Neurologic examination consistent these symptoms. Serial brain MRIs demonstrated development a subcortical, multifocal T2/fluid-attenuated inversion recovery hyperintensity left frontoparietal white matter (figure 1). Subtle but definite MRI abnormalities were present same area 12 prior. His clinical course findings prompted urgent evaluation