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首页> 外文期刊>European journal of paediatric neurology: EJPN : official journal of the European Paediatric Neurology Society >Brain anomalies in 121 children with non-syndromic single suture craniosynostosis by MR imaging
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Brain anomalies in 121 children with non-syndromic single suture craniosynostosis by MR imaging

机译:MR影像学检查121例非综合征性单缝颅缝综合征患者的脑部异常

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摘要

Introduction: The aim of this study was to evaluate prevalence of intracranial abnormalities in children with non-syndromic single suture craniosynostosis scheduled for cranial vault remodelling surgery using pre-operative magnetic resonance imaging. Patients and methods: A retrospective analysis of brain magnetic resonance imaging studies of 129 non-syndromic single suture craniosynostosis children undergoing craniofacial surgery between January, 2004-October, 2010 was conducted. Statistical analysis was performed for child, maternal and sibling related predisposing factors for abnormal brain magnetic resonance imaging findings. The mean age of these 121 patients at the time of imaging was 21.6 months. The majority, 78% were males and 74% of the patients were scaphocephalic. Results: In 18 (15%) patients abnormal brain findings were noted. The most common finding was Chiari 1 malformation in 11 (9%). Chiari 1 malformation comprised over half (61%) of the brain anomalies identified. None of these findings required any additional surgical procedures. None of the statistical analysis reached statistical significance. Conclusions: Brain anomalies in connection with non-syndromic single suture craniosynostosis patients seem to be a coincidental event. We did not establish any specific craniosynostosis form to be regularly associated with abnormal brain magnetic resonance imaging findings. The routine use of pre-operative magnetic resonance imaging in non-syndromic single suture craniosynostosis patients seems to be of limited value in the search for associated intracranial malformations necessitating additional interventions.
机译:简介:这项研究的目的是通过术前磁共振成像评估计划进行颅穹改建手术的非综合征性单线缝线颅骨融合症患儿颅内异常的患病率。患者和方法:回顾性分析了2004年1月至2010年10月之间接受颅面外科手术的129例非综合征性单缝线颅骨合缝症儿童的脑磁共振成像研究。对儿童,母亲和兄弟姐妹相关的诱发脑磁共振成像异常的诱发因素进行统计分析。这121例患者在成像时的平均年龄为21.6个月。多数为男性,78%为男性,74%为头颅型患者。结果:在18(15%)位患者中,发现了异常的大脑发现。最常见的发现是11例Chiari 1畸形(9%)。 Chiari 1畸形占所识别出的大脑异常的一半以上(61%)。这些发现均不需要任何其他外科手术程序。统计分析均未达到统计学意义。结论:与非综合征性单缝线颅骨融合症患者相关的脑部异常似乎是一个偶然事件。我们没有建立任何特定的颅前突增生形式来定期与异常的脑磁共振成像结果相关联。对于非综合征性单线缝隙性颅骨融合症患者,术前磁共振成像的常规使用在寻找相关颅内畸形方面的价值有限,因此需要采取其他干预措施。

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