模拟室管膜瘤的髓内神经鞘瘤:说明性病例。

Takayasu Ando, Hisaaki Uchikado, Natsuko Miyahara, Satoshi Nagase, Takehiro Makizono, Jin Kikuchi, Gohsuke Hattori, Motohiro Morioka
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引用次数: 0

摘要

背景:大多数髓内脊髓肿瘤为胶质瘤,如星形细胞瘤和室管膜瘤。髓内神经鞘瘤很少见。观察:一名73岁女性,表现为缓慢进行性腿部麻木和步态紊乱。MRI造影诊断为T10-11型髓内室管膜瘤。在电生理监测下经后正中沟入路行肿瘤切除。肿瘤病理为神经鞘瘤。术后,患者改良McCormick评分等级恶化(II级至III级)。经验教训:如果后正中沟移位,应怀疑脊髓室管膜瘤。在这种情况下应考虑后外侧沟入路。https://thejns.org/doi/10.3171/CASE25127。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intramedullary schwannoma mimicking ependymoma: illustrative case.

Background: Most intramedullary spinal cord tumors are gliomas such as astrocytoma and ependymoma. Intramedullary schwannoma is rare.

Observations: A 73-year-old woman presented with slowly progressive leg numbness and disturbed gait. A T10-11 intramedullary ependymoma was diagnosed by contrast-enhanced MRI. Tumor resection was performed via the posterior median sulcus approach under electrophysiological monitoring. Tumor pathology was schwannoma. After surgery, the patient's modified McCormick Scale grade worsened (grade II to grade III).

Lessons: Spinal cord ependymoma should be suspected if the posterior median sulcus is displaced. A posterolateral sulcus approach should be considered in such cases. https://thejns.org/doi/10.3171/CASE25127.

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