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一例成人硬脊膜内髓内颈段脊髓神经肠囊肿罕见病例:病例展示

A rare case of intradural intramedullary cervical spinal neurenteric cyst in an adult: illustrative case.

作者信息

Porto Carl, Thakrar Raj, Abdulrazeq Hael, Teshome Abigail, Ramesh Navin, Dailey Jennifer, Rosenberg Harry, Fridley Jared

机构信息

The Warren Alpert School of Medicine, Brown University, Providence, Rhode Island.

Department of Neurosurgery, Rhode Island Hospital, The Warren Alpert School of Medicine, Brown University, Providence, Rhode Island.

出版信息

J Neurosurg Case Lessons. 2025 Jun 30;9(26). doi: 10.3171/CASE25253.

Abstract

BACKGROUND

Neurenteric cysts are rare congenital lesions of the CNS, typically found in the cervical or thoracic spine and presenting in early life. Only 5% of spinal neurenteric cysts are intramedullary. The authors report the case of an intradural intramedullary neurenteric cyst in a 68-year-old woman.

OBSERVATIONS

The patient presented with 4 months of progressive left extremity numbness, weakness, and imbalance consistent with cervical myelopathy. MRI revealed a 1-cm cystic lesion in the intradural intramedullary cervical spine. Multilevel posterior cervical laminectomy for cyst resection was performed with gross-total resection. Histopathological analysis revealed squamous, columnar, and pseudostratified epithelium positive for epithelial membrane antigen and cytokeratin and negative for glial fibrillary acidic protein and S100 protein, consistent with a neurenteric cyst. Her symptoms and examination significantly improved after surgery.

LESSONS

Neurenteric cysts comprise 1% of spinal lesions, and 5% are intradural intramedullary. Symptoms progress gradually but may fluctuate with cyst size changes. MRI is the preferred imaging, with histopathological analysis required for diagnosis. Operative intervention for gross-total resection is the recommended management. This case emphasizes that neurenteric cysts should be considered in older adults with cervical myelopathy and a cystic intramedullary mass and demonstrates the benefit of complete surgical removal. https://thejns.org/doi/10.3171/CASE25253.

摘要

背景

神经肠囊肿是中枢神经系统罕见的先天性病变,通常见于颈椎或胸椎,在生命早期出现。仅5%的脊柱神经肠囊肿位于髓内。作者报告了一例68岁女性的硬膜内髓内神经肠囊肿病例。

观察结果

患者出现4个月的进行性左侧肢体麻木、无力和失衡,符合颈椎病。磁共振成像(MRI)显示颈椎硬膜内髓内有一个1厘米的囊性病变。行多节段颈椎后路椎板切除术以切除囊肿,实现了全切。组织病理学分析显示,鳞状、柱状和假复层上皮上皮膜抗原和细胞角蛋白呈阳性,胶质纤维酸性蛋白和S100蛋白呈阴性,符合神经肠囊肿。术后她的症状和检查结果明显改善。

经验教训

神经肠囊肿占脊柱病变的1%,其中5%为硬膜内髓内病变。症状逐渐进展,但可能随囊肿大小变化而波动。MRI是首选的影像学检查,诊断需要组织病理学分析。建议的治疗方法是手术干预以实现全切。该病例强调,对于患有颈椎病和髓内囊性肿块的老年人应考虑神经肠囊肿,并证明了完全手术切除的益处。https://thejns.org/doi/10.3171/CASE25253。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/742b/12210062/cf7a895697ec/CASE25253_figure_1.jpg

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