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智力发育迟缓儿童的磁共振成像

MRI in children with mental retardation.

作者信息

Soto-Ares Gustavo, Joyes Béatrice, Lemaître Marie-Pierre, Vallée Louis, Pruvo Jean-Pierre

机构信息

Department of Neuroradiology, Hôpital Roger Salengro, CHRU Lille, 59037 Lille, France.

出版信息

Pediatr Radiol. 2003 May;33(5):334-45. doi: 10.1007/s00247-003-0891-z. Epub 2003 Mar 11.

Abstract

BACKGROUND

In mental retardation (MR) an aetiological diagnosis is not always obtained despite a detailed history, physical examination and metabolic or genetic investigations. In some of these patients, MRI is recommended and may identify subtle abnormal brain findings.

OBJECTIVE

We reviewed the cerebral MRI of children with non-specific mental retardation in an attempt to establish a neuroanatomical picture of this disorder.

MATERIALS AND METHODS

Thirty children with non-specific MR were selected to undergo cerebral MRI. The examination included supratentorial axial slices, mid-sagittal images and posterior fossa coronal images. Brain malformations, midline and cerebellar abnormalities were studied.

RESULTS

In 27 of 30 patients, the neuroimaging evaluation revealed a relatively high incidence of cerebral and posterior fossa abnormalities. The most frequent were: dysplasia of the corpus callosum (46%; hypoplasia, short corpus callosum and vertical splenium), partially opened septum pellucidum and/or cavum vergae (33%), ventriculomegaly (33%), cerebral cortical dysplasia (23%), subarachnoid space enlargement (16.6%), vermian hypoplasia (33%), cerebellar and/or vermian disorganised folia (20%), and subarachnoid spaces enlargement in the posterior fossa (20%). Other anomalies were: enlarged Virchow-Robin spaces (10%), white matter anomalies (10%) and cerebellar or vermian atrophy.

CONCLUSIONS

MRI has shown a high incidence of subtle cerebral abnormalities and unexpected minor forms of cerebellar cortical dysplasia. Even if most of these abnormalities are considered as subtle markers of brain dysgenesis, their role in the pathogenesis of mental retardation needs further investigation.

摘要

背景

在智力发育迟缓(MR)中,尽管进行了详细的病史询问、体格检查以及代谢或基因检查,病因诊断仍不总是能够得出。在其中一些患者中,推荐进行MRI检查,其可能会发现细微的脑部异常表现。

目的

我们回顾了非特异性智力发育迟缓儿童的脑部MRI检查结果,试图建立这种疾病的神经解剖学图像。

材料与方法

选取30例非特异性MR儿童进行脑部MRI检查。检查包括幕上轴位切片、正中矢状位图像和后颅窝冠状位图像。对脑畸形、中线和小脑异常进行研究。

结果

在30例患者中的27例中,神经影像学评估显示脑和后颅窝异常的发生率相对较高。最常见的异常包括:胼胝体发育异常(46%;发育不全、胼胝体短小和压部垂直)、透明隔部分开放和/或穹窿腔(33%)、脑室扩大(33%)、大脑皮质发育异常(23%)、蛛网膜下腔增宽(16.6%)、蚓部发育不全(33%)、小脑和/或蚓部小叶结构紊乱(20%)以及后颅窝蛛网膜下腔增宽(20%)。其他异常包括:血管周围间隙增宽(10%)、白质异常(10%)以及小脑或蚓部萎缩。

结论

MRI显示出细微脑异常和意外的小脑皮质发育异常轻微形式的高发生率。即使这些异常中的大多数被认为是脑发育异常的细微标志,它们在智力发育迟缓发病机制中的作用仍需进一步研究。

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