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[透明隔腔和穹窿间腔患儿的脑部磁共振成像数据]

[MRI brain imaging data in children with cavum septi pellucidi and vergae].

作者信息

Kaciński Marek, Kubik Alicja, Herman-Sucharska Izabela, Paciorek Anna, Kroczka Sławomir, Zajac Anna

机构信息

Klinika Neurologii Dziecigcej, Uniwersytetu Jagiellońskiego, Collegium Medicum, Kraków.

出版信息

Przegl Lek. 2007;64(11):923-8.

Abstract

BACKGROUND

Cavum septum pellucidum (CSP) is commonly known marker of neurodevelopmental brain malformation. In MR imaging it is seen either as an isolated finding or with association of others developmental brain changes e.g. cavum vergae (CV).

AIM OF THE STUDY

was to assess the frequency of CSP and CV associated with others brain developmental malformations in children. We also classified clinical syndromes in children with these structural brain malformations.

MATERIAL AND METHODS

The study was performed on 55 children, hospitalised in the Department of Pediatric Neurology, Jagiellonian University in Krakow, between 1998-2006 with diagnosed CSP and/or CV in MRI. There were 29 girls and 26 boys aged 4 months-16 years old. Clinical history, clinical status and neurological findings in physical examination were main indication to perform brain MRI. MRI scans was done in SE T1, FSE T2, PD, FLAIR, IR T1 sequences, 3 and 5 mm depth, in vertical, frontal and axial surfaces, performed on 1,5 T machine Signa Horizon HiSpeed General Electric.

RESULTS

There were 38 children with CSP, 12 children with CSP and CV, and 5 with CV. In 18/55 children (33%) CSP was isolated, but in 37/55 children (67%) CSP was coexisted with other brain structural malformations. The average age of diagnosis in isolated CSP was 10 years old, in coexisting malformation was 5 years. In half of the children, the reason of neuroimaging was epilepsy, in this 6/18 patient with isolated CSP or CV. 58% of the study group had a normal mental development, but 35% of children with additional brain malformation and 11% of children with isolated CSP and CV were mentally retarded.

CONCLUSION

  1. The majority of the children with CSP and CV had also coexisting brain malformations diagnosed in MRI. 2. CSP and CV coexisting with large brain malformation e.g. dysplasia septo-optica and agenesis of corpus callosum. were diagnosed earlier. 4. Mental retardation was diagnosed in 1/3 children with different structural brain malformation but also in 11% of children with CSP and CV as well.
摘要

背景

透明隔腔(CSP)是常见的神经发育性脑畸形标志物。在磁共振成像中,它可表现为孤立性发现,或与其他脑部发育改变如透明隔腔(CV)相关联。

研究目的

评估儿童中CSP和CV与其他脑部发育畸形相关的频率。我们还对患有这些脑部结构畸形的儿童的临床综合征进行了分类。

材料与方法

该研究对1998年至2006年间在克拉科夫雅盖隆大学儿科神经科住院的55名儿童进行,这些儿童在磁共振成像中被诊断出患有CSP和/或CV。其中有29名女孩和26名男孩,年龄在4个月至16岁之间。临床病史、临床状况和体格检查中的神经学发现是进行脑部磁共振成像的主要指征。磁共振成像扫描采用SE T1、FSE T2、PD、FLAIR、IR T1序列,层厚3毫米和5毫米,在垂直、冠状和轴位面上进行,使用1.5T的通用电气Signa Horizon HiSpeed机器。

结果

有38名儿童患有CSP,12名儿童同时患有CSP和CV,5名儿童患有CV。在18/55名儿童(33%)中,CSP是孤立性的,但在37/55名儿童(67%)中,CSP与其他脑部结构畸形共存。孤立性CSP的平均诊断年龄为10岁,合并畸形的为5岁。在一半的儿童中,神经影像学检查的原因是癫痫,其中6/18例为孤立性CSP或CV患者。研究组中58%的儿童智力发育正常,但35%的合并其他脑部畸形的儿童和11%的孤立性CSP和CV儿童存在智力发育迟缓。

结论

  1. 大多数患有CSP和CV的儿童在磁共振成像中也被诊断出合并有脑部畸形。2. CSP和CV与严重的脑部畸形如视隔发育不良和胼胝体发育不全共存。3. (此处原文似乎缺失内容)4. 三分之一患有不同脑部结构畸形的儿童以及11%患有CSP和CV的儿童被诊断为智力发育迟缓。

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