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表现为布朗 - 塞卡尔综合征的特发性横贯性脊髓炎。

Idiopathic transverse myelitis presenting as the Brown-Sequard syndrome.

作者信息

Moon S-J, Lee J-K, Kim T-W, Kim S-H

机构信息

Department of Neurosurgery, Chonnam National University Hospital and Medical School, Gwangju, Korea.

出版信息

Spinal Cord. 2009 Feb;47(2):176-8. doi: 10.1038/sc.2008.23. Epub 2008 Mar 11.

Abstract

STUDY DESIGN

Case report.

OBJECTIVES

To report an unusual case of Brown-Sequard syndrome (BSS) associated with idiopathic transverse myelitis (TM).

SETTING

Department of Neurosurgery, Chonnam National University Hospital, Gwangju, South Korea.

METHODS

A 38-year-old man presented with left leg weakness and right-sided decrease in sensation at the T11 level below. Magnetic resonance images (MRI) of the thoracic spine showed diffuse swelling of the spinal cord spanning the fifth to the eighth thoracic vertebra. The lesion had high signal intensity on T2-weighted images. Eccentric nodular enhancement within the left anterolateral aspect of the spinal cord was appreciated with gadolinium administration.

RESULTS

The patient was treated with pulsed methylprednisone and showed marked improvement in neurological function within 3 days. An MRI at 5-month follow-up demonstrated complete resolution of the abnormalities.

CONCLUSION

This case illustrates a rare case of BSS caused by idiopathic TM of the thoracic spinal cord. TM should be considered in the differential diagnosis of BSS.

摘要

研究设计

病例报告。

目的

报告一例与特发性横贯性脊髓炎(TM)相关的罕见布朗 - 塞卡尔综合征(BSS)病例。

背景

韩国光州全南国立大学医院神经外科。

方法

一名38岁男性出现左腿无力及T11水平以下右侧感觉减退。胸椎磁共振成像(MRI)显示脊髓弥漫性肿胀,累及胸5至胸8椎体。该病变在T2加权图像上呈高信号强度。静脉注射钆剂后可见脊髓左前外侧偏心结节状强化。

结果

患者接受脉冲式甲泼尼龙治疗,3天内神经功能显著改善。5个月随访时的MRI显示异常完全消退。

结论

本病例说明了由胸段脊髓特发性TM引起的罕见BSS病例。在BSS的鉴别诊断中应考虑TM。

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