视神经脊髓炎后恢复行走和皮质脊髓束兴奋性1例

Hui-Ting Shih , Hui-Ting Goh , Seema Sikka , Rita Hamilton , Chad Swank
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引用次数: 0

摘要

视神经脊髓炎谱系障碍(NMOSD)是一种罕见的自身免疫性疾病,引起轴突损伤并伴有相应的功能缺陷。在本病例报告中,我们前瞻性地跟踪了一名确诊为NMOSD的女性患者在住院康复(IPR)后6个月的行走恢复和皮质脊髓兴奋性。她在家庭和社区环境中恢复了独立行走功能。经颅磁刺激获得的神经生理测量显示两种时间演化模式。在恢复早期,皮质内抑制明显减少,皮质内促进明显增加,而在IPR出院后6个月,皮质脊髓通路兴奋性明显增加。
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Regaining walking and restoring corticospinal tract excitability after neuromyelitis optica spectrum disorder: A case report

Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease causing axonal damage with corresponding functional deficits. In this case report, we prospectively tracked walking recovery and corticospinal excitability of a female diagnosed with NMOSD through six months after her inpatient rehabilitation (IPR) stay. She recovered independent walking function in home and community settings. Neurophysiological measures acquired using transcranial magnetic stimulation showed two temporal evolution patterns. There was a remarkably reduced intra-cortical inhibition and increased intra-cortical facilitation at the early recovery phase whereas increased corticospinal pathway excitability was noted at 6 months after IPR discharge.

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