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儿童厚胼胝体

Thick Corpus Callosum in Children.

作者信息

Schupper Aviv, Konen Osnat, Halevy Ayelet, Cohen Rony, Aharoni Sharon, Shuper Avinoam

机构信息

Department of Pediatric Neurology and Epilepsy Center, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

出版信息

J Clin Neurol. 2017 Apr;13(2):170-174. doi: 10.3988/jcn.2017.13.2.170.

DOI:10.3988/jcn.2017.13.2.170
PMID:28406584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5392459/
Abstract

BACKGROUND AND PURPOSE

A thick corpus callosum (TCC) can be associated with a very grave outcome in fetuses, but its clinical presentation in older children seems to be markedly different.

METHODS

The corpus callosum (CC) was defined as thick based on observations and impressions. We reviewed cases of children who were diagnosed as TCC based on brain magnetic resonance imaging (MRI) studies. The pertinent clinical data of these children were collected, and their CCs were measured.

RESULTS

Out of 2,552 brain MRI images, those of 37 children were initially considered as showing a TCC. Those initial imaging were reviewed by an experienced neuroradiologist, who confirmed the diagnosis in 34 children (1.3%): 13 had neurofibromatosis-1 (NF-1), 9 had epilepsy, 3 had macrocephaly capillary malformation (MCM) syndrome, 3 had autistic spectrum disorder, 1 had a Chiari-1 malformation, and 1 had increased head circumference. No specific neurologic disorder could be defined in seven children. The measured thickness of the CC in these children was comparable to those published in the literature for adults.

CONCLUSIONS

A TCC is a rare brain malformation that can be found in neuropathologies with apparently diverse pathognomonic mechanisms, such as NF-1 and MCM. It is not necessarily associated with life-threatening conditions, instead being a relatively benign finding, different in nature from that reported in fetuses.

摘要

背景与目的

胎儿胼胝体增厚(TCC)可能与非常严重的后果相关,但在大龄儿童中的临床表现似乎明显不同。

方法

基于观察和印象将胼胝体(CC)定义为增厚。我们回顾了根据脑磁共振成像(MRI)研究诊断为TCC的儿童病例。收集了这些儿童的相关临床数据,并测量了他们的CC。

结果

在2552份脑MRI图像中,最初有37名儿童的图像被认为显示TCC。这些初始图像由一位经验丰富的神经放射科医生进行了复查,确诊34名儿童(1.3%)患有TCC:13名患有神经纤维瘤病1型(NF-1),9名患有癫痫,3名患有巨头毛细血管畸形(MCM)综合征,3名患有自闭症谱系障碍,1名患有Chiari-1畸形,1名头围增大。7名儿童未发现特定的神经系统疾病。这些儿童测量的CC厚度与文献中报道的成人厚度相当。

结论

TCC是一种罕见的脑畸形,可在具有明显不同病理机制的神经病理学中发现,如NF-1和MCM。它不一定与危及生命的情况相关,相反是一个相对良性的发现,其本质与胎儿中报道的不同。

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本文引用的文献

1
Congenital and acquired abnormalities of the corpus callosum: a pictorial essay.胼胝体先天性和获得性异常:影像学研究。
Biomed Res Int. 2013;2013:265619. doi: 10.1155/2013/265619. Epub 2013 Aug 6.
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Comparison of cranial magnetic resonance imaging findings and clinical features in patients with corpus callosum abnormalities.胼胝体异常患者的头颅磁共振成像结果与临床特征比较
Neuropediatrics. 2014 Feb;45(1):30-5. doi: 10.1055/s-0033-1349228. Epub 2013 Jul 25.
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Biometry of the fetal corpus callosum by three-dimensional ultrasound.三维超声对胎儿胼胝体的生物测量。
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Imaging spectrum of pediatric corpus callosal pathology: a pictorial review.儿童胼胝体病变的影像学表现:影像学综述。
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Thick corpus callosum: a clue to the diagnosis of fetal septopreoptic holoprosencephaly?胼胝体增厚:胎儿前脑无裂畸形的诊断线索?
Pediatr Radiol. 2012 Jul;42(7):886-90. doi: 10.1007/s00247-011-2260-7. Epub 2011 Oct 18.
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Connectivity and the corpus callosum in autism spectrum conditions: insights from comparison of autism and callosal agenesis.自闭症谱系障碍的连接与胼胝体:自闭症与胼胝体发育不全的比较研究的启示。
Prog Brain Res. 2011;189:303-17. doi: 10.1016/B978-0-444-53884-0.00031-2.
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Megalencephaly, mega corpus callosum, and complete lack of motor development: delineation of a rare syndrome.巨脑回、巨大胼胝体和完全缺乏运动发育:一种罕见综合征的描绘。
Am J Med Genet A. 2010 Sep;152A(9):2360-4. doi: 10.1002/ajmg.a.33577.
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The development of the corpus callosum in the healthy human brain.胼胝体在健康人脑内的发育。
J Neurosci. 2010 Aug 18;30(33):10985-90. doi: 10.1523/JNEUROSCI.5122-09.2010.
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Corpus callosum morphology and its relationship to cognitive function in neurofibromatosis type 1.1型神经纤维瘤病中胼胝体形态及其与认知功能的关系。
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Thick fetal corpus callosum: an ominous sign?胎儿胼胝体增宽:不祥之兆?
Ultrasound Obstet Gynecol. 2009 Jul;34(1):55-61. doi: 10.1002/uog.6356.