Hyperostotic meningiomas in children. A case-based update.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY Child's Nervous System Pub Date : 2024-12-11 DOI:10.1007/s00381-024-06708-x
Fulvio Grilli, Hamzah Youssef Smaili, Federico Bianchi, Paolo Frassanito, Gianpiero Tamburrini, Luca Massimi
{"title":"Hyperostotic meningiomas in children. A case-based update.","authors":"Fulvio Grilli, Hamzah Youssef Smaili, Federico Bianchi, Paolo Frassanito, Gianpiero Tamburrini, Luca Massimi","doi":"10.1007/s00381-024-06708-x","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Meningiomas are rare tumors in children compared with adults. Their main peculiarities are the frequent convexity or intraventricular location, the common association with neurofibromatosis-2 (NF-2) and the relatively high rate of aggressive and/or hyperostotic variants. Hyperostosis may complicate the surgical management. The goal of this paper is to provide an update on the main characteristics and the management of hyperostotic meningiomas.</p><p><strong>Case description: </strong>A 7-year-old girl was admitted to our department because of a long-lasting history of left frontal skull bulging. Neuroimaging examinations revealed a huge hyperostotic meningioma with bony invasion and infiltration of the superior sagittal sinus. Genetic tests were positive for NF-2. The tumor (atypical meningioma) was gross totally resected. During the same operation, a custom-made cranioplasty was realized with the help of a frame-based craniectomy. The patient is asymptomatic and under oncological follow-up.</p><p><strong>Discussion and conclusion: </strong>Although generally rare, hyperostotic meningiomas are relatively common in children and clinically demanding because of their large size, the possible aggressive behavior and the need of a cranioplasty as additional surgical step. Therefore, a careful preoperative surgical planning is required, taking into account that the extent of surgical resection is an important prognostic factor. The long-term outcome is good.</p>","PeriodicalId":9970,"journal":{"name":"Child's Nervous System","volume":"41 1","pages":"43"},"PeriodicalIF":1.3000,"publicationDate":"2024-12-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Child's Nervous System","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00381-024-06708-x","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Meningiomas are rare tumors in children compared with adults. Their main peculiarities are the frequent convexity or intraventricular location, the common association with neurofibromatosis-2 (NF-2) and the relatively high rate of aggressive and/or hyperostotic variants. Hyperostosis may complicate the surgical management. The goal of this paper is to provide an update on the main characteristics and the management of hyperostotic meningiomas.

Case description: A 7-year-old girl was admitted to our department because of a long-lasting history of left frontal skull bulging. Neuroimaging examinations revealed a huge hyperostotic meningioma with bony invasion and infiltration of the superior sagittal sinus. Genetic tests were positive for NF-2. The tumor (atypical meningioma) was gross totally resected. During the same operation, a custom-made cranioplasty was realized with the help of a frame-based craniectomy. The patient is asymptomatic and under oncological follow-up.

Discussion and conclusion: Although generally rare, hyperostotic meningiomas are relatively common in children and clinically demanding because of their large size, the possible aggressive behavior and the need of a cranioplasty as additional surgical step. Therefore, a careful preoperative surgical planning is required, taking into account that the extent of surgical resection is an important prognostic factor. The long-term outcome is good.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
儿童肥厚性脑膜瘤。基于案例的更新。
背景:儿童脑膜瘤是一种少见的肿瘤。它们的主要特点是常呈凸状或位于脑室内,常与神经纤维瘤病-2 (NF-2)相关,侵袭性和/或增厚变异的发生率相对较高。骨质增生可能使手术治疗复杂化。本文的目的是提供一个更新的主要特点和管理的肥厚脑膜瘤。病例描述:一名7岁女童因左额颅骨长时间突出入住我科。神经影像学检查显示一个巨大的骨质增生脑膜瘤,并伴有骨侵犯和上矢状窦浸润。基因检测NF-2呈阳性。肿瘤(非典型脑膜瘤)全部切除。在同一手术中,在框架颅骨切除术的帮助下实现了定制的颅骨成形术。患者无症状,正在接受肿瘤随访。讨论与结论:虽然通常罕见,但肥大脑膜瘤在儿童中相对常见,由于其体积大,可能的侵袭性行为以及需要颅骨成形术作为额外的手术步骤,临床要求很高。因此,考虑到手术切除的程度是一个重要的预后因素,需要仔细的术前手术计划。长期结果是好的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Child's Nervous System
Child's Nervous System 医学-临床神经学
CiteScore
3.00
自引率
7.10%
发文量
322
审稿时长
3 months
期刊介绍: The journal has been expanded to encompass all aspects of pediatric neurosciences concerning the developmental and acquired abnormalities of the nervous system and its coverings, functional disorders, epilepsy, spasticity, basic and clinical neuro-oncology, rehabilitation and trauma. Global pediatric neurosurgery is an additional field of interest that will be considered for publication in the journal.
期刊最新文献
Do routine antibiotics change the myelomeningocele infection rate? A case series. Rare regression of congenital brainstem high-grade glioma: case report and literature review. Primary diffuse leptomeningeal atypical teratoid/rhabdoid tumours (ATRT) of childhood: a molecularly characterised case report and literature review. Comparison of failure rates between full-barium and striped barium distal shunt catheters: a matched case-control study. Comparative analysis of treatment modalities for pediatric spinal cord glioblastoma: insights from a meta-analysis.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1