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延髓分裂合并多发神经管闭合性缺陷。

Split medulla in association with multiple closed neural tube defects.

作者信息

Muroi Ai, Fleming Karen L, McComb J Gordon

机构信息

Division of Neurosurgery, Childrens Hospital Los Angeles, Suite 1006, Los Angeles, CA 90027, USA.

出版信息

Childs Nerv Syst. 2010 Jul;26(7):967-71. doi: 10.1007/s00381-010-1098-x. Epub 2010 Feb 24.

Abstract

PURPOSE

We describe the case of a patient with a split medulla associated with multiple closed neural tube defects.

CASE REPORT

This 13-year-old female initially presented to our service at just over a year of age for neck abnormalities and a congenital midline occipital dermal sinus. MRI and CT scans showed the presence of multiple cervical vertebral segmentation abnormalities, a bony spur at the level of the craniocervical junction, split medulla, split cervical spinal cord, and a midline occipital dermal sinus. Since the patient's neurological course had remained stable during follow-up for over 11 years, the only surgical procedure undertaken was excision of the dermal sinus to prevent infection.

CONCLUSIONS

The constellation of abnormalities indicates that the notochord was split early during gestation, both rostral and caudal to the cervicomedullary junction. Surgical intervention to treat the other malformations needs to be considered only if the patient develops a progressive neurological deficit.

摘要

目的

我们描述了一例伴有多处闭合性神经管缺陷的延髓分裂患者的病例。

病例报告

这名13岁女性在一岁多一点时因颈部异常和先天性枕部中线皮肤窦首次前来就诊。磁共振成像(MRI)和计算机断层扫描(CT)显示存在多处颈椎节段异常、颅颈交界处的骨质增生、延髓分裂、颈髓分裂以及枕部中线皮肤窦。由于患者在超过11年的随访期间神经病程保持稳定,所以仅进行了切除皮肤窦以预防感染的手术。

结论

这一系列异常表明脊索在妊娠早期于颈髓交界处的头侧和尾侧均发生了分裂。仅当患者出现进行性神经功能缺损时才需要考虑手术干预来治疗其他畸形。

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