Current state of spinal nerve sheath tumor management and future advances

IF 3.7 Q1 CLINICAL NEUROLOGY
Chloe Gui, Luxshikka Canthiya, Gelareh Zadeh, S. Suppiah
{"title":"Current state of spinal nerve sheath tumor management and future advances","authors":"Chloe Gui, Luxshikka Canthiya, Gelareh Zadeh, S. Suppiah","doi":"10.1093/noajnl/vdae067","DOIUrl":null,"url":null,"abstract":"\n Nerve sheath tumors are the most common benign tumors of the spine after meningiomas. They include schwannomas, neurofibroma, and malignant peripheral nerve sheath tumors. These can arise sporadically or in association with tumor predisposition syndromes, including Neurofibromatosis type 1, Neurofibromatosis type 2, and Schwannomatosis. Though surgery is the traditional mainstay of treatment for these tumors, the discovery of the genetic and molecular basis of these diseases in recent decades has prompted investigation into targeted therapies. Here, we give a clinical overview of spinal nerve sheath tumors, their imaging features, current management practices, and explore ongoing advances in systemic therapies.","PeriodicalId":94157,"journal":{"name":"Neuro-oncology advances","volume":null,"pages":null},"PeriodicalIF":3.7000,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuro-oncology advances","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1093/noajnl/vdae067","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Nerve sheath tumors are the most common benign tumors of the spine after meningiomas. They include schwannomas, neurofibroma, and malignant peripheral nerve sheath tumors. These can arise sporadically or in association with tumor predisposition syndromes, including Neurofibromatosis type 1, Neurofibromatosis type 2, and Schwannomatosis. Though surgery is the traditional mainstay of treatment for these tumors, the discovery of the genetic and molecular basis of these diseases in recent decades has prompted investigation into targeted therapies. Here, we give a clinical overview of spinal nerve sheath tumors, their imaging features, current management practices, and explore ongoing advances in systemic therapies.
脊神经鞘瘤的治疗现状和未来进展
神经鞘瘤是继脑膜瘤之后最常见的脊柱良性肿瘤。它们包括分裂瘤、神经纤维瘤和恶性周围神经鞘瘤。这些肿瘤可能是散发性的,也可能与肿瘤易感综合征有关,包括神经纤维瘤病 1 型、神经纤维瘤病 2 型和许旺瘤病。虽然手术是治疗这些肿瘤的传统主要方法,但近几十年来对这些疾病的遗传和分子基础的发现促使人们开始研究靶向疗法。在此,我们将对脊神经鞘瘤的临床概况、影像学特征、当前的治疗方法进行概述,并探讨系统疗法的最新进展。
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 求助全文
来源期刊
CiteScore
6.20
自引率
0.00%
发文量
0
审稿时长
12 weeks
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信