[横贯脊髓炎20多年后复发1例,怀疑为视神经脊髓炎谱系障碍]。

Q4 Medicine
Clinical Neurology Pub Date : 2025-07-25 Epub Date: 2025-06-26 DOI:10.5692/clinicalneurol.cn-002108
Toshiyuki Mizukura, Yu Sugiyama
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引用次数: 0

摘要

患者是一位78岁的女性。在X-23年,她出现步态障碍和胸部以下感觉障碍,被诊断为急性横贯脊髓炎并接受治疗。神经系统症状在X-22年复发,怀疑为视脊髓多发性硬化症(OSMS)。随后,她没有经历神经症状的复发;然而,x年患者出现左侧面瘫,双上肢感觉异常,左下肢肌肉无力。MRI显示病变从延髓延伸至C6水平,血清aqp4抗体检测阳性,诊断为视神经脊髓炎频谱障碍。本病例是视神经脊髓炎谱系障碍长期复发的典型病例,具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case of recurrence after more than 20 years from transverse myelitis suspected to be neuromyelitis optica spectrum disorder].

This patient was a 78-year-old woman. In year X-23, she presented with gait disturbance and sensory impairment below the chest level and was diagnosed with and treated for acute transverse myelitis. The neurological symptoms recurred in year X-22, and she was treated under suspicion of opticospinal multiple sclerosis (OSMS). Subsequently, she did not experience a relapse of neurological symptoms; however, she developed left facial paralysis, abnormal sensations in both upper limbs, and muscle weakness in the left lower limb in year X. MRI revealed lesions extending from the medulla oblongata to the C6 level, and serum testing was positive for anti-AQP4 antibodies, leading to a diagnosis of neuromyelitis optica spectrum disorder. This case was considered clinically significant as an example of neuromyelitis optica spectrum disorder recurrence after a long period.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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