Spinal Neurenteric Cyst of the Ventral Cervicothoracic Junction With Klippel-Feil Syndrome as a Symptom of Progressive Myelopathy: A Case Report.

Q3 Medicine Korean Journal of Neurotrauma Pub Date : 2024-03-11 eCollection Date: 2024-03-01 DOI:10.13004/kjnt.2024.20.e8
Jong Tae Lee, Myeong Jin Ko, Hee Sung Kim, Seung Won Park, Young-Seok Lee
{"title":"Spinal Neurenteric Cyst of the Ventral Cervicothoracic Junction With Klippel-Feil Syndrome as a Symptom of Progressive Myelopathy: A Case Report.","authors":"Jong Tae Lee, Myeong Jin Ko, Hee Sung Kim, Seung Won Park, Young-Seok Lee","doi":"10.13004/kjnt.2024.20.e8","DOIUrl":null,"url":null,"abstract":"<p><p>Neurenteric cysts are rare and account for only 0.7%-1.3% of all spinal tumors. Spinal neurenteric cysts are associated with spina bifida, split-cord malformations, and Klippel-Feil syndrome, a rare congenital disorder characterized by fusion of two or more cervical vertebrae. Klippel-Feil syndrome is rarely accompanied by neurenteric cysts. In this case report, we describe a cervicothoracic junction neurenteric cyst associated with Klippel-Feil syndrome in a 30-year-old man who presented with a 2-month history of neck pain with radiation of pain into both arms and a 1-month history of weakness in the left arm. Magnetic resonance imaging (MRI) of the spine revealed an expansive intradural extramedullary cystic lesion anterior to the spinal cord at the cervicothoracic junction. The neurenteric cyst was removed using an anterior approach, accompanied by C5-C6 corpectomy. The patient's condition improved postoperatively, and he was discharged after postoperative MRI. Spinal neurenteric cysts should be considered in the differential diagnosis in cases of vertebral developmental abnormalities concurrent with intraspinal cysts.</p>","PeriodicalId":36879,"journal":{"name":"Korean Journal of Neurotrauma","volume":"20 1","pages":"69-74"},"PeriodicalIF":0.0000,"publicationDate":"2024-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10990689/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Korean Journal of Neurotrauma","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13004/kjnt.2024.20.e8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Neurenteric cysts are rare and account for only 0.7%-1.3% of all spinal tumors. Spinal neurenteric cysts are associated with spina bifida, split-cord malformations, and Klippel-Feil syndrome, a rare congenital disorder characterized by fusion of two or more cervical vertebrae. Klippel-Feil syndrome is rarely accompanied by neurenteric cysts. In this case report, we describe a cervicothoracic junction neurenteric cyst associated with Klippel-Feil syndrome in a 30-year-old man who presented with a 2-month history of neck pain with radiation of pain into both arms and a 1-month history of weakness in the left arm. Magnetic resonance imaging (MRI) of the spine revealed an expansive intradural extramedullary cystic lesion anterior to the spinal cord at the cervicothoracic junction. The neurenteric cyst was removed using an anterior approach, accompanied by C5-C6 corpectomy. The patient's condition improved postoperatively, and he was discharged after postoperative MRI. Spinal neurenteric cysts should be considered in the differential diagnosis in cases of vertebral developmental abnormalities concurrent with intraspinal cysts.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
颈胸交界处脊髓神经源性囊肿伴有作为进行性脊髓病症状的 Klippel-Feil 综合征:病例报告。
神经管囊肿非常罕见,仅占所有脊柱肿瘤的 0.7%-1.3%。脊髓神经管囊肿与脊柱裂、脊髓分裂畸形和克利珀尔-费尔综合征有关,克利珀尔-费尔综合征是一种罕见的先天性疾病,其特征是两个或多个颈椎融合。克利珀尔-费尔综合征很少伴有神经节囊肿。在本病例报告中,我们描述了一名 30 岁男性的颈胸交界处神经软骨囊肿与 Klippel-Feil 综合征的相关性,该患者有 2 个月的颈部疼痛病史,疼痛可放射至双臂,并有 1 个月的左臂无力病史。脊柱磁共振成像(MRI)显示,颈胸交界处脊髓前方有一个膨胀性硬膜外囊肿病变。患者采用前路手术切除了神经根囊肿,同时进行了C5-C6椎体切除术。患者术后情况有所好转,术后核磁共振检查后出院。在椎体发育异常并发椎管内囊肿的病例中,应将脊髓神经节囊肿考虑在鉴别诊断中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
1.10
自引率
0.00%
发文量
41
期刊最新文献
Letter to the Editor: Commentary on Acute Paraparesis Caused by Spinal Epidural Fluid After Balloon Kyphoplasty for Traumatic Avascular Necrosis: A Case Report (Korean J Neurotrauma 2023;19:398-402). Should Hypertonic Saline Be Considered for the Treatment of Intracranial Hypertension? A Review of Current Evidence and Clinical Practices. Pain Intervention for Osteoporotic Compression Fracture, From Physical Therapy to Surgery: A Literature Review. KJNT Symposium 2024: A Starting Point for a Leap Forward. Feasibility Study of Parkinson's Speech Disorder Evaluation With Pre-Trained Deep Learning Model for Speech-to-Text Analysis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1