Connectome imaging to facilitate preservation of the frontal aslant tract.

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY
Harshal A Shah, Laura Mittelman, Souvik Singha, Rosivel Galvez, Julianna Cavallaro, Beril Yaffe, Grace Huang, Justin W Silverstein, Randy S D'Amico
{"title":"Connectome imaging to facilitate preservation of the frontal aslant tract.","authors":"Harshal A Shah, Laura Mittelman, Souvik Singha, Rosivel Galvez, Julianna Cavallaro, Beril Yaffe, Grace Huang, Justin W Silverstein, Randy S D'Amico","doi":"10.1016/j.clineuro.2025.108726","DOIUrl":null,"url":null,"abstract":"<p><p>Supplementary motor area (SMA) syndrome is characterized by contralateral akinesia and mutism, and frequently occurs following resection of tumors involving the superior frontal gyrus. The frontal aslant tract (FAT), involved in functional connectivity of the supplementary area and other related large-scale brain networks, is implicated in the pathogenesis of, and recovery from, SMA syndrome. However, intraoperative neuromonitoring of the FAT is inconsistent and poorly reproducible, leading to a high rate of postoperative SMA syndrome. We report the cases of two patients harboring lesions of the superior frontal gyrus: one cavernoma and one low grade glioma. Connectome imaging revealed involvement of functional networks implicated in SMA syndrome, as well as displacement of the FAT. A connectome-guided awake craniotomy was performed in both cases, and a combinatorial approach using awake language mapping and connectome-imaging guidance facilitated gross total resection of both patient's lesions without inducing SMA syndrome postoperatively. Functional and structural connectivity imaging through connectomics allows the identification of areas not traditionally considered eloquent, such as the SMA and FAT, and can help facilitate their preservation. Conserving the functional and structural connectivity of broader brain regions that are not traditionally deemed eloquent can improve patient outcomes.</p>","PeriodicalId":10385,"journal":{"name":"Clinical Neurology and Neurosurgery","volume":"249 ","pages":"108726"},"PeriodicalIF":1.8000,"publicationDate":"2025-01-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Neurology and Neurosurgery","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.clineuro.2025.108726","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Supplementary motor area (SMA) syndrome is characterized by contralateral akinesia and mutism, and frequently occurs following resection of tumors involving the superior frontal gyrus. The frontal aslant tract (FAT), involved in functional connectivity of the supplementary area and other related large-scale brain networks, is implicated in the pathogenesis of, and recovery from, SMA syndrome. However, intraoperative neuromonitoring of the FAT is inconsistent and poorly reproducible, leading to a high rate of postoperative SMA syndrome. We report the cases of two patients harboring lesions of the superior frontal gyrus: one cavernoma and one low grade glioma. Connectome imaging revealed involvement of functional networks implicated in SMA syndrome, as well as displacement of the FAT. A connectome-guided awake craniotomy was performed in both cases, and a combinatorial approach using awake language mapping and connectome-imaging guidance facilitated gross total resection of both patient's lesions without inducing SMA syndrome postoperatively. Functional and structural connectivity imaging through connectomics allows the identification of areas not traditionally considered eloquent, such as the SMA and FAT, and can help facilitate their preservation. Conserving the functional and structural connectivity of broader brain regions that are not traditionally deemed eloquent can improve patient outcomes.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Clinical Neurology and Neurosurgery
Clinical Neurology and Neurosurgery 医学-临床神经学
CiteScore
3.70
自引率
5.30%
发文量
358
审稿时长
46 days
期刊介绍: Clinical Neurology and Neurosurgery is devoted to publishing papers and reports on the clinical aspects of neurology and neurosurgery. It is an international forum for papers of high scientific standard that are of interest to Neurologists and Neurosurgeons world-wide.
×
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