...
首页> 外文期刊>Internet Journal of Pediatrics and Neonatology >Cervical meningocele with tethered cord in a seven-years old child: Case Report
【24h】

Cervical meningocele with tethered cord in a seven-years old child: Case Report

机译:一名七岁儿童的颈部脊髓带束缚脊髓性脑膜膨出:病例报告

获取原文
           

摘要

Meningoceles are typically associated with other congenital spinal anomalies, and are usuallydiagnosed in childhood. Cervical meningoceles are extremely uncommon congenital spinal anomalies. Most patients have no neurological deficit at presentation and treatment has been mainly cosmetic. Treatment aims to prevent future neurological deterioration, and should include careful intradural exploration with untethering of the cord. We report a case of cervical meningocele in a 7-year-old girl. The tethering band, confirmed intra-operatively. Untethering of the cord was performed together with resection of the sac and repair of the dura. Early intervention is recommended even in cases with normal neurological examinations in order to prevent deterioration. These cases should be operated as soon as possible after birth. Introduction Cervical meningoceles and myelomeningoceles account for only 4% to 8% of spina bifida cystica lesions. Cervical meningoceles comprise only a small proportion of neural tube defects [123]. A meningocele is a single, posteriorly herniating cystic sac. The sac is cerebrospinal fluid filled and is lined by arachnoid and dura [4]. There may be a band of tissue that tents the posterior aspect of the cervical cord and extends into the wall of the sac either to the base or the dome [5]. A small number of reports have noted that meningoceles may feature associated tethering of the cervical spinal cord [126].In this report, we presented a 7 year-old patient harboring a meningocel in the upper cervical region with neurological deficit and tethered cord. The lesion was treated surgically. Case History A 7-years-old girl suffering from a posterior mass in the cervical region was admitted to our clinic (Figure 1).
机译:脑膜膨出症通常与其他先天性脊柱畸形相关,通常在儿童时期被诊断。子宫颈脑膜膨出是极少见的先天性脊柱畸形。大多数患者在就诊时没有神经功能缺损,治疗主要是美容。治疗的目的是防止将来的神经系统恶化,并且应包括在不松动绳索的情况下进行仔细的硬膜内探查。我们报告了一名7岁女孩的宫颈脑膜膨出病例。系留带,术中证实。脐带的束缚与囊的切除和硬脑膜的修复一起进行。即使在神经系统检查正常的情况下,也建议尽早干预以防止恶化。这些病例应在出生后尽快进行手术。引言宫颈脑膜膨出和脊髓膜脑膨出仅占脊柱裂囊肿病变的4%至8%。颈脑膜膨出仅占神经管缺损的一小部分[123]。脑膜膨出是单个的,后突出的囊性囊。囊内充满脑脊液,内衬蛛网膜和硬脑膜[4]。可能有一条组织带束住颈索的后部,并延伸到囊壁至基部或圆顶[5]。少数报告指出脑膜膨出可能与颈脊髓束缚有关[126]。在本报告中,我们介绍了一名7岁的患者,该患者在上颈区有脑膜囊肿,伴有神经功能缺损和系绳。病变已通过手术治疗。病例历史一名7岁的女孩在颈部区域患有后部肿块,被送入我们的诊所(图1)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号