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先天性脑积水患儿颅骨的额孔

Frontal foramina in pediatric skull in cases of congenital hydrocephalus.

作者信息

Sun J K, LeMay D R, Couldwell W T, Zee C

机构信息

Department of Neuroradiology, University of Southern California, Los Angeles County Hospital 90033, USA.

出版信息

Radiology. 1995 Nov;197(2):497-9. doi: 10.1148/radiology.197.2.7480701.

Abstract

PURPOSE

To describe a new observation, frontal calvarial foramina, in pediatric patients with congenital hydrocephalus secondary to central nervous system malformation.

MATERIALS AND METHODS

Frontal foramina were initially identified in three female patients with Chiari II malformation. Subsequently, head computed tomographic (CT) scans in 99 patients with congenital hydrocephalus were retrospectively reviewed. CT scans in a control group of 116 patients without hydrocephalus were also retrospectively reviewed.

RESULTS

Frontal foramina were found in eight of 61 (13%) patients with Chiari II malformation, in one child with Dandy-Walker malformation, and in one child with occipital horn dilatation (colpocephaly), but not in control patients. Sequential CT examinations in three patients with frontal foramina depicted gradual closure after ventriculoperitoneal shunt placement.

CONCLUSION

Frontal foramina may represent an abnormality variably expressed in certain central nervous system malformations that cause congenital hydrocephalus. The presence of frontal foramina palpated or visualized on plain radiographs may help in the diagnosis of congenital hydrocephalus and central nervous system malformation.

摘要

目的

描述在继发于中枢神经系统畸形的先天性脑积水小儿患者中一种新发现的额骨孔。

材料与方法

最初在3例患有Chiari II畸形的女性患者中发现额骨孔。随后,对99例先天性脑积水患者的头部计算机断层扫描(CT)进行回顾性分析。还对116例无脑积水的对照组患者的CT扫描进行回顾性分析。

结果

在61例(13%)患有Chiari II畸形的患者中有8例发现额骨孔,在1例患有Dandy-Walker畸形的患儿和1例患有枕角扩张(脑室后部积水)的患儿中发现额骨孔,但对照组患者未发现。对3例有额骨孔的患者进行的连续CT检查显示,在脑室腹腔分流术后额骨孔逐渐闭合。

结论

额骨孔可能代表在某些导致先天性脑积水的中枢神经系统畸形中可变表达的一种异常。在平片上可触及或看到的额骨孔可能有助于先天性脑积水和中枢神经系统畸形的诊断。

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