Komatsu Junji, Sakai Kenji, Nakada Mitsutoshi, Iwasa Kazuo, Yamada Masahito
Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa 920-8640, Japan.
Department of Neurosurgery, Kanazawa University Hospital, 13-1 Takara-machi, Kanazawa 920-8640, Japan.
J Clin Neurosci. 2017 Aug;42:106-108. doi: 10.1016/j.jocn.2017.03.022. Epub 2017 Apr 29.
Multiple sclerosis (MS) is an inflammatory demyelinating disease of the central nervous system. We report the case of a 50-year-old man who presented with progressive gait ataxia. Brain magnetic resonance imaging (MRI) on fluid-attenuated inversion recovery revealed a hyperintense lesion in the right temporal white matter. The spinal cord showed a long hyperintense lesion between the vertebral levels C6 and L1 on T2-weighted MRI. Biopsied tissues from the brain lesion demonstrated features of inflammatory demyelination with preservation of astrocytes, consistent with typical MS. This is the first reported case of pathologically proven MS with longitudinally extensive spinal cord lesions.
多发性硬化症(MS)是一种中枢神经系统的炎性脱髓鞘疾病。我们报告了一例50岁男性患者,其表现为进行性步态共济失调。液体衰减反转恢复序列的脑部磁共振成像(MRI)显示右侧颞叶白质有一个高信号病变。脊髓在T2加权MRI上显示C6至L1椎体水平之间有一个长的高信号病变。脑病变的活检组织显示出伴有星形胶质细胞保留的炎性脱髓鞘特征,与典型的MS一致。这是首例经病理证实的伴有纵向广泛脊髓病变的MS病例。