Suppr超能文献

Chiari I型畸形中枕骨基底部发育不全的发生率:后颅窝的比较形态计量学研究。临床文章。

Incidence of basioccipital hypoplasia in Chiari malformation type I: comparative morphometric study of the posterior cranial fossa. Clinical article.

作者信息

Noudel Rémy, Jovenin Nicolas, Eap Cristophe, Scherpereel Bernard, Pierot Laurent, Rousseaux Pascal

机构信息

Department of Neurosurgery, Maison Blanche Hospital, University of Reims, France.

出版信息

J Neurosurg. 2009 Nov;111(5):1046-52. doi: 10.3171/2009.2.JNS08284.

Abstract

OBJECT

The chronic tonsillar herniation defining Chiari malformation Type I (CMI) is thought to result from overcrowding of a normally developing hindbrain within a congenitally small posterior cranial fossa (PCF) due to occipital hypoplasia. The goals in the present study were to authenticate the cranioencephalic disproportion in a group of patients with CMI and to discuss new developmental aspects according to which part of the occipital bone was underdeveloped.

METHODS

The authors retrospectively examined a group of 17 patients with CMI. Measurements of osteotentorial and neural structures of the PCF were made on MR images of the brain. The results were compared with findings in 30 healthy controls by using the Mann-Whitney U-test.

RESULTS

Dimensions of the neural structures did not differ between the 2 groups of patients. The mean length of the basiocciput was significantly shorter in the CMI group (19.4 mm) compared with the control group (25.7 mm; p = 0.0003). The mean diameter of the foramen magnum was larger in the CMI group, but this difference was not statistically significant. The dimensions of the supraocciput and the mean angle of the cerebellar tentorium were identical in the 2 groups.

CONCLUSIONS

Data in this study support the idea that occipital hypoplasia is the main cause of overcrowding within the PCF. Basioccipital shortness is a cardinal feature of the resultant shallow PCF and could proceed from a congenital disorder of the cephalic mesoderm of the parachordal plate or occur later in the infancy because of premature stenosis of the sphenooccipital synchondrosis.

摘要

目的

I型 Chiari 畸形(CMI)所定义的慢性扁桃体疝被认为是由于枕骨发育不全,正常发育的后脑在先天性小后颅窝(PCF)内过度拥挤所致。本研究的目的是验证一组CMI患者的颅-脑比例失调情况,并根据枕骨发育不全的部位探讨新的发育方面的问题。

方法

作者回顾性研究了一组17例CMI患者。在脑部磁共振成像上测量PCF的骨-小脑幕和神经结构。通过Mann-Whitney U检验将结果与30名健康对照者的结果进行比较。

结果

两组患者的神经结构尺寸没有差异。CMI组的枕骨基部平均长度(19.4mm)明显短于对照组(25.7mm;p = 0.0003)。CMI组的枕骨大孔平均直径较大,但这种差异无统计学意义。两组的枕骨上部尺寸和小脑幕平均角度相同。

结论

本研究数据支持枕骨发育不全是PCF内过度拥挤的主要原因这一观点。枕骨基部短小是由此产生的浅后颅窝的主要特征,可能源于脊索旁板头侧中胚层的先天性疾病,或因蝶枕软骨结合过早狭窄而在婴儿期后期出现。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验