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具有常见骨质形态的I型脊髓纵裂畸形

Type I split cord malformation with an usual bony morphology.

作者信息

Shokouhi G, Tubbs R S, Shoja M M

机构信息

Department of Neurosurgery, University of Tabriz, Tabriz, Iran.

出版信息

Folia Morphol (Warsz). 2007 Feb;66(1):78-9.

Abstract

Variations in the configuration of the bony septum found in patients with split cord malformations are rare. We report the seemingly rare occurrence of a midline bony septum that ended posteriorly as a fully formed bony spinous process. We speculate that this variation is due to misplaced mesodermal cells associated with the primitive endomesenchymal tract during approximately the third week of foetal life. The clinician that manages these patients may wish to consider this rare morphology and avoid excessive manipulation of such a process, which could potentially injure an underlying hemicord.

摘要

在脊髓纵裂畸形患者中发现的骨隔形态变异很罕见。我们报告了一种看似罕见的中线骨隔情况,其向后终止于一个完全形成的棘突。我们推测这种变异是由于在胎儿生命大约第三周时,与原始内胚层间质束相关的中胚层细胞位置异常所致。治疗这些患者的临床医生可能希望考虑这种罕见的形态,并避免对这样一个结构进行过度操作,因为这可能会潜在地损伤下方的半侧脊髓。

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