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
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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.

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。
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CiteScore
1.10
自引率
0.00%
发文量
41
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