肺神经内分泌肿瘤引起硬膜外脊髓压迫和经硬膜髓内侵犯的外科治疗:一个说明性病例。

Wesley Shoap, Kion Gregory, Jack A Leoni, Gabriel C Tender
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引用次数: 0

摘要

背景:髓内脊髓转移是一种非常罕见的事件。因此,缺乏关于手术干预时机、类型和程度的具体指导。观察:一名60岁男性,患有已知的肺神经内分泌肿瘤,表现为2天进行性下肢截瘫,使他无法行动。MRI显示肿块经胸膜和椎旁侵入,并延伸至左侧T1-2和T2-3神经孔,造成明显的硬膜外压迫。T2处也有经硬膜侵袭,延伸髓内至C4脊柱水平,并伴有脊髓水肿。他接受了后颈胸椎板切除术和经椎弓根硬膜外肿瘤切除术。髓内组件未被移除。他接受了辅助放疗和化疗,在6个月的随访中,他的下肢运动功能明显恢复,可以用助行器行走。经验教训:本病例表明,快速手术减压即使对侵袭性肿瘤造成硬膜外和髓内侵袭也能提供益处。是否切除髓内假体应根据具体情况,结合患者的神经学检查和影像学表现来决定。https://thejns.org/doi/10.3171/CASE25200。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Surgical management of a pulmonary neuroendocrine tumor causing epidural spinal cord compression and transdural intramedullary invasion: illustrative case.

Background: Intramedullary spinal cord metastasis from local transdural invasion is an exceedingly rare event. Therefore, specific guidance on the timing, type, and extent of surgical intervention is lacking.

Observations: A 60-year-old male with a known pulmonary neuroendocrine tumor presented with 2 days of progressive lower extremity paraplegia rendering him nonambulatory. MRI demonstrated transpleural and paravertebral invasion by the mass with extension through the left T1-2 and T2-3 neural foramina causing significant epidural compression. There was also transdural invasion at T2 extending intramedullary to the C4 spinal level, with associated cord edema. He underwent posterior cervicothoracic laminectomy and fusion with transpedicular epidural tumor debulking. The intramedullary component was not removed. He received adjuvant radiation therapy and chemotherapy and at the 6-month follow-up demonstrated significant return of motor function in his lower extremities, ambulating with a walker.

Lessons: This case illustrates that rapid surgical decompression can still provide benefit even for aggressive tumors causing transdural and intramedullary invasion. The decision on whether to remove the intramedullary component should be made on a case-by-case basis and guided by the patient's neurological examination in combination with imaging findings. https://thejns.org/doi/10.3171/CASE25200.

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