• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

癫痫作为一名儿童中与胼胝体发育不全相关的神经胶质囊肿的一种表现形式。

Epilepsy as a Presentation of a Neuroglial Cyst Associated with Dysgenesis of Corpus Callosum in a Child.

作者信息

Mustapha Outznit, Allali Nazik, Latifa Chat, El Haddad Siham

机构信息

Pediatric Radiology Department, Rabat Children's Hospital, Avicenne University Hospital, Morocco.

出版信息

Case Rep Radiol. 2021 Jan 21;2021:6675071. doi: 10.1155/2021/6675071. eCollection 2021.

DOI:10.1155/2021/6675071
PMID:33552610
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7847349/
Abstract

Neuroglial (glioependymal) cyst is a rare congenital tumor of the central nervous system usually found in childhood. It can be isolated or associated with other brain malformations. Magnetic resonance imaging is the technique of choice for making the diagnosis. We report the case of a 10-year-old child who presented with epileptic seizures revealing a neuroglial cyst and dysgenesis of the corpus callosum.

摘要

神经胶质（室管膜胶质）囊肿是一种罕见的中枢神经系统先天性肿瘤，通常在儿童期发现。它可以是孤立的，也可与其他脑畸形相关。磁共振成像是进行诊断的首选技术。我们报告一例10岁儿童病例，该患儿因癫痫发作就诊，检查发现有神经胶质囊肿和胼胝体发育不全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d2/7847349/8fddfe3cae19/CRIRA2021-6675071.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d2/7847349/069be5553e4f/CRIRA2021-6675071.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d2/7847349/8fddfe3cae19/CRIRA2021-6675071.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d2/7847349/069be5553e4f/CRIRA2021-6675071.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33d2/7847349/8fddfe3cae19/CRIRA2021-6675071.002.jpg

相似文献

1
Epilepsy as a Presentation of a Neuroglial Cyst Associated with Dysgenesis of Corpus Callosum in a Child.癫痫作为一名儿童中与胼胝体发育不全相关的神经胶质囊肿的一种表现形式。
Case Rep Radiol. 2021 Jan 21;2021:6675071. doi: 10.1155/2021/6675071. eCollection 2021.
2
[Associated brain anomalies and clinical findings in corpus callosum dysgenesis].胼胝体发育不全相关的脑异常及临床发现
Tani Girisim Radyol. 2003 Dec;9(4):411-7.
3
Fetal MRI demonstrates glioependymal cyst in a case of sonographic unilateral ventriculomegaly.胎儿磁共振成像显示一例超声检查发现单侧脑室扩大病例中的室管膜下囊肿。
Pediatr Radiol. 2007 Apr;37(4):391-5. doi: 10.1007/s00247-007-0419-z. Epub 2007 Feb 8.
4
[Corpus callosum agenesis and epileptic seizures].[胼胝体发育不全与癫痫发作]
Rev Neurol. 1999 Jan;28 Suppl 1:S6-13.
5
Lipoma with Agenesis of Corpus Callosum: 2 Case Reports and Literature Review.脂肪瘤伴胼胝体发育不全：2例报告及文献复习
World Neurosurg. 2019 May;125:123-125. doi: 10.1016/j.wneu.2019.01.088. Epub 2019 Jan 28.
6
[Lipoma of calm body revealed by a convulsive crisis: about a case].[惊厥发作揭示的平静身体脂肪瘤：病例报告]
Pan Afr Med J. 2020 Apr 7;35:101. doi: 10.11604/pamj.2020.35.101.20440. eCollection 2020.
7
Interhemispheric glioependymal cyst associated with agenesis of the corpus callosum--case report.与胼胝体发育不全相关的半球间胶质室管膜囊肿——病例报告
Neurol Med Chir (Tokyo). 2000 Oct;40(10):536-42. doi: 10.2176/nmc.40.536.
8
Interhemispheric multiloculated ependymal cyst with dysgenesis of the corpus callosum: a case in a preterm fetus.伴有胼胝体发育不全的半球间多房性室管膜囊肿：一例早产胎儿病例
Childs Nerv Syst. 2007 Jul;23(7):807-13. doi: 10.1007/s00381-006-0275-4. Epub 2007 Mar 27.
9
Altered integrity of corpus callosum in generalized epilepsy in relation to seizure lateralization after corpus callosotomy.胼胝体切开术后，与致痫灶偏侧化相关的全面性癫痫胼胝体完整性改变。
Neurosurg Focus. 2020 Apr 1;48(4):E15. doi: 10.3171/2020.1.FOCUS19791.
10
[Intramedullary neuroglial cyst: a case report].
Neurochirurgie. 2012 Oct;58(5):320-4. doi: 10.1016/j.neuchi.2009.10.001. Epub 2012 Jun 14.

引用本文的文献

1
Pediatric third ventricular glioependymal cyst: A case report.小儿第三脑室胶质室管膜囊肿：一例报告。
Surg Neurol Int. 2025 Feb 28;16:64. doi: 10.25259/SNI_814_2024. eCollection 2025.
2
Neuroepithelial cyst causing homonymous hemianopia treated through surgical marsupialization under visual-evoked potentials: A case report.通过视觉诱发电位引导下手术造袋术治疗导致同向性偏盲的神经上皮囊肿：病例报告
Surg Neurol Int. 2024 Nov 15;15:419. doi: 10.25259/SNI_529_2024. eCollection 2024.
3
Giant supra and retrosellar glioependymal cyst presenting with only precocious puberty. Clinical study and review of the literature.

本文引用的文献

1
A large interhemispheric glioependymal cyst associated with partial defect of the corpus callosum in an elderly man.一名老年男性存在大脑半球间大的胶质室管膜囊肿，伴有胼胝体部分缺损。
Neuropathology. 2020 Oct;40(5):496-500. doi: 10.1111/neup.12661. Epub 2020 Jul 14.
2
Neuroendoscopic fenestration of glioependymal cysts to the ventricle: report of 3 cases.
J Neurosurg. 2018 Nov 30;131(5):1615-1619. doi: 10.3171/2018.7.JNS172501. Print 2019 Nov 1.
3
Intracranial glioependymal (neuroglial) cysts: a systematic review.颅内胶质室管膜（神经胶质）囊肿：一项系统评价
仅以性早熟为表现的巨大鞍上和鞍后胶质室管膜囊肿。临床研究及文献复习
Int J Surg Case Rep. 2024 Mar;116:109360. doi: 10.1016/j.ijscr.2024.109360. Epub 2024 Feb 21.
Acta Neurochir (Wien). 2018 Jul;160(7):1439-1449. doi: 10.1007/s00701-018-3566-0. Epub 2018 May 25.
4
Porencephalic cyst: a rare cause of new-onset seizure in an adult.脑穿通畸形囊肿：成人新发癫痫的罕见病因。
J Community Hosp Intern Med Perspect. 2018 Apr 17;8(2):92-93. doi: 10.1080/20009666.2018.1454788. eCollection 2018.
5
Hemiatrophy as a presentation of a glioependymal cyst.
Clin Neurol Neurosurg. 2014 Sep;124:6-7. doi: 10.1016/j.clineuro.2014.06.005. Epub 2014 Jun 19.
6
Glioependymal cyst in children: a case report.儿童胶质室管膜囊肿：一例报告
Clin Neurol Neurosurg. 2013 Oct;115(10):2288-90. doi: 10.1016/j.clineuro.2013.07.036. Epub 2013 Aug 6.
7
Intracranial cysts: radiologic-pathologic correlation and imaging approach.颅内囊肿：放射学与病理学的相关性及影像学检查方法
Radiology. 2006 Jun;239(3):650-64. doi: 10.1148/radiol.2393050823.
8
Congenital porencephaly: MR features and relationship to hippocampal sclerosis.先天性脑穿通畸形：磁共振成像特征及其与海马硬化的关系。
AJNR Am J Neuroradiol. 1998 Jan;19(1):135-41.