Suppr超能文献

室管膜下结节性异位、额鼻脑膨出、胼胝体发育不全和蛛网膜囊肿:一名癫痫患儿的一系列异常表现。

Periventricular nodular heterotopia, frontonasal encephalocele, corpus callosal dysgenesis and arachnoid cyst: A constellation of abnormalities in a child with epilepsy.

作者信息

Krishnan Prasad, Chattopadhyay Arijit, Saha Manash

机构信息

Department of Neurosurgery, National Neurosciences Centre, Peerless Hospital Complex, Panchasayar, Kolkata, West Bengal, India.

Department of Neurology, National Neurosciences Centre, Peerless Hospital Complex, Panchasayar, Kolkata, West Bengal, India.

出版信息

J Pediatr Neurosci. 2014 Sep-Dec;9(3):273-5. doi: 10.4103/1817-1745.147591.

Abstract

A 7-year-old male child presented with poorly controlled generalized tonic-clonic seizures. On examination, he was mentally retarded, deaf and had a swelling at the root on the nose. Computed tomography scan done previously revealed a left temporal arachnoid cyst (AC) due to which he was referred for surgery. However, magnetic resonance imaging revealed a constellation of abnormalities - all of which could be responsible for his seizures. The combination of periventricular nodular heterotopias with encepaholcele is rarely described in the literature, and more infrequently so its combination with AC and callosal dysgenesis - the Chudley-Mccullough syndrome. We describe the case and review relevant literature on this subject.

摘要

一名7岁男童出现全身性强直阵挛性癫痫发作,控制不佳。检查发现,他智力发育迟缓、失聪,鼻根部有肿胀。此前进行的计算机断层扫描显示左侧颞叶蛛网膜囊肿(AC),因此他被转诊接受手术。然而,磁共振成像显示出一系列异常——所有这些都可能是其癫痫发作的原因。脑室周围结节性异位合并脑膨出的情况在文献中很少被描述,而其与AC和胼胝体发育不全的合并情况则更少见——即Chudley-Mccullough综合征。我们描述了该病例并回顾了关于这一主题的相关文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69f0/4302553/9f194ef583aa/JPN-9-273-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验