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圆锥部伴脊髓纵裂畸形的无症状神经肠囊肿:病例报告及文献复习

Silent neurenteric cyst with split cord malformation at conus medullaris: Case report and literature review.

作者信息

Srinivas Hanuma, Kumar Ashish

机构信息

Department of Neurosurgery, Nizam's Institute of Medical Sciences, Hyderabad, Telangana, India.

出版信息

J Pediatr Neurosci. 2014 Sep-Dec;9(3):246-8. doi: 10.4103/1817-1745.147579.

Abstract

Split cord malformations (SCM) are a common pediatric abnormality where children present with features of tethering and backache along with varying neurological deficits. Multiple neural tube defects may co-exist in children having defects of primary and/or secondary neurulation. Co-existent neurenteric cysts along with type 1 SCM have been described very rarely in the literature. We report a case of silent neurenteric cyst at conus medullaris with SCM type 1 where the cyst was missed in the preoperative imaging. Until date, only 8 such cases of neurenteric cysts with SCM at lumbar region have been reported. We review the literature regarding co-existing dual pathologies of neurenteric cysts and type 1 SCMs in light of limited capacity of imaging modalities to detect small neurenteric cysts in presence of co-existent neural tube defects. Multiple spinal neural tube defects in children need more attention and precise microneurosurgical skills as management differs in each of them. Co-existence of such pathologies detected intra-operatively may need modifications in preoperative planning to achieve the best possible outcomes.

摘要

脊髓纵裂畸形(SCM)是一种常见的儿科异常疾病,患儿表现为脊髓栓系和背痛症状,同时伴有不同程度的神经功能缺损。原发性和/或继发性神经管形成缺陷的儿童可能同时存在多种神经管缺陷。文献中很少描述1型SCM合并神经肠囊肿的情况。我们报告一例圆锥部无症状神经肠囊肿合并1型SCM的病例,术前影像学检查漏诊了该囊肿。迄今为止,仅报道了8例腰椎区域神经肠囊肿合并SCM的病例。鉴于在存在神经管缺陷的情况下,成像方式检测小神经肠囊肿的能力有限,我们回顾了有关神经肠囊肿和1型SCM并存的双重病理的文献。儿童多发性脊髓神经管缺陷需要更多关注以及精确的显微神经外科技术,因为每种缺陷的治疗方法不同。术中检测到此类病变并存可能需要对术前规划进行调整,以实现最佳治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f3/4302545/570619086964/JPN-9-246-g001.jpg

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