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C1神经根的延髓颈髓海绵状畸形:病例展示

Cervicomedullary cavernous malformation of the C1 nerve root: illustrative case.

作者信息

Zhang Yi, Yuan Lorenzo, Marianayagam Neelan J, Kumar Kevin K, Fatemi Parastou, Park David J, Chang Steven D

机构信息

Department of Neurosurgery, Stanford University School of Medicine, Stanford, California.

Department of Neurological Surgery, Cleveland Clinic, Cleveland, Ohio.

出版信息

J Neurosurg Case Lessons. 2024 Jul 29;8(5). doi: 10.3171/CASE2456.

Abstract

BACKGROUND

Cavernous malformations (CMs) originating from spinal nerve roots are rare but can present with rapidly progressing neurological deficits. Therefore, quick identification and treatment are essential.

OBSERVATIONS

The authors present the case of a 52-year-old male presenting with headaches and gait disturbance, found to have a CM of the C1 nerve root. The patient underwent successful suboccipital craniectomy and C1 laminectomy, with complete resection of the lesion, preservation of the cervical spinal nerve roots, and symptomatic improvement postoperatively.

LESSONS

This is the first presentation in the literature of a CM originating from the C1 nerve root. The authors show complete resection of the lesion with preservation of the C1 nerve root. Nerve root lesions usually show insidious symptomatic onset. Quick identification and resection are recommended to prevent permanent neurological disability. https://thejns.org/doi/10.3171/CASE2456.

摘要

背景

起源于脊神经根的海绵状畸形(CMs)较为罕见,但可表现为迅速进展的神经功能缺损。因此,快速识别和治疗至关重要。

观察结果

作者报告了一例52岁男性,表现为头痛和步态障碍,发现患有C1神经根海绵状畸形。患者接受了成功的枕下开颅术和C1椎板切除术,病变完全切除,颈脊神经根得以保留,术后症状改善。

经验教训

这是文献中首次报道起源于C1神经根的海绵状畸形。作者展示了在保留C1神经根的情况下完全切除病变。神经根病变通常起病隐匿,症状逐渐出现。建议快速识别并切除病变以预防永久性神经功能残疾。https://thejns.org/doi/10.3171/CASE2456

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7068/11301600/4ff5222bef59/CASE2456_figure_1.jpg

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