Strategies in the Management of Lower Cranial Nerve Schwannomas: Insights From the Gruppo Otologico.

IF 1.4
Melcol Hailu Yilala, Giuseppe Fancello, Lucia Bélen Musumano, Gianluca Piras, Lorenzo Lauda, Yi Sun, Fernando Mancini, Luca Morelli, Mario Sanna
{"title":"Strategies in the Management of Lower Cranial Nerve Schwannomas: Insights From the Gruppo Otologico.","authors":"Melcol Hailu Yilala, Giuseppe Fancello, Lucia Bélen Musumano, Gianluca Piras, Lorenzo Lauda, Yi Sun, Fernando Mancini, Luca Morelli, Mario Sanna","doi":"10.1227/ons.0000000000001981","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>Jugular foramen schwannoma is a rare benign tumor arising from the lower cranial nerves. After reviewing their experience with microsurgical management of jugular foramen schwannomas through lateral skull base and transcervical approaches, the authors recommend a management algorithm to direct simplified surgical management.</p><p><strong>Methods: </strong>Cases of jugular foramen schwannomas treated by the senior author between 1983 and 2024 were analyzed retrospectively. Sociodemographic data, clinical presentation, radiological and intraoperative tumor characteristics, histopathological results, surgical approaches, and postoperative course until the last visit were thoroughly documented and analyzed.</p><p><strong>Results: </strong>A total of 53 cases of jugular foramen tumors were treated over a 40-year period. Age at presentation ranged from 13 to 76 years, with a mean age of 42.84 years. Women comprised 53% (n = 28) of the total patients operated on, whereas the rest, 47% (n = 25), were men. The most common presenting symptoms were hearing loss and dysphagia. Tumors were classified according to the Kaye and Pellet classification system into classes A (11.32%), B (39.62%), C (15.09%), and D (33.96%). The most commonly used surgical approach was the petro-occipital trans-sigmoid approach, either alone or combined with other approaches, and gross total removal was achieved in 98% of patients. New postoperative paralysis in previously normal lower cranial nerve function was evident in 44% (n = 8) of patients who had normal lower cranial nerve function before surgery. The duration of follow-up ranged from 12 to 144 months, with a mean follow-up period of 63.46 months. Three patients (5.6%) had tumor recurrence.</p><p><strong>Conclusion: </strong>Based on their experience, the authors have proposed a treatment algorithm that guides the best surgical strategy. Even if gross total tumor removal of jugular foramen area lesions can safely be achieved nowadays, an extensive understanding of microsurgical anatomy of the area and surgical training is mandatory.</p>","PeriodicalId":520730,"journal":{"name":"Operative neurosurgery (Hagerstown, Md.)","volume":" ","pages":"852-864"},"PeriodicalIF":1.4000,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Operative neurosurgery (Hagerstown, Md.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1227/ons.0000000000001981","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/3/13 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background and objectives: Jugular foramen schwannoma is a rare benign tumor arising from the lower cranial nerves. After reviewing their experience with microsurgical management of jugular foramen schwannomas through lateral skull base and transcervical approaches, the authors recommend a management algorithm to direct simplified surgical management.

Methods: Cases of jugular foramen schwannomas treated by the senior author between 1983 and 2024 were analyzed retrospectively. Sociodemographic data, clinical presentation, radiological and intraoperative tumor characteristics, histopathological results, surgical approaches, and postoperative course until the last visit were thoroughly documented and analyzed.

Results: A total of 53 cases of jugular foramen tumors were treated over a 40-year period. Age at presentation ranged from 13 to 76 years, with a mean age of 42.84 years. Women comprised 53% (n = 28) of the total patients operated on, whereas the rest, 47% (n = 25), were men. The most common presenting symptoms were hearing loss and dysphagia. Tumors were classified according to the Kaye and Pellet classification system into classes A (11.32%), B (39.62%), C (15.09%), and D (33.96%). The most commonly used surgical approach was the petro-occipital trans-sigmoid approach, either alone or combined with other approaches, and gross total removal was achieved in 98% of patients. New postoperative paralysis in previously normal lower cranial nerve function was evident in 44% (n = 8) of patients who had normal lower cranial nerve function before surgery. The duration of follow-up ranged from 12 to 144 months, with a mean follow-up period of 63.46 months. Three patients (5.6%) had tumor recurrence.

Conclusion: Based on their experience, the authors have proposed a treatment algorithm that guides the best surgical strategy. Even if gross total tumor removal of jugular foramen area lesions can safely be achieved nowadays, an extensive understanding of microsurgical anatomy of the area and surgical training is mandatory.

下颅神经鞘瘤的治疗策略:来自耳科小组的见解。
背景与目的:颈静脉孔神经鞘瘤是一种罕见的起源于下颅神经的良性肿瘤。在回顾了通过侧颅底和经颈入路显微外科治疗颈静脉孔神经鞘瘤的经验后,作者推荐了一种指导简化手术治疗的管理算法。方法:回顾性分析资深作者1983 ~ 2024年收治的颈静脉孔神经鞘瘤病例。社会人口学数据、临床表现、放射学和术中肿瘤特征、组织病理学结果、手术入路和术后过程直到最后一次就诊都被彻底记录和分析。结果:在40多年的时间里,共治疗了53例颈静脉孔肿瘤。发病年龄13 ~ 76岁,平均42.84岁。女性占手术患者总数的53% (n = 28),其余47% (n = 25)为男性。最常见的症状是听力丧失和吞咽困难。根据Kaye和Pellet分类系统将肿瘤分为A(11.32%)、B(39.62%)、C(15.09%)和D(33.96%)。最常用的手术入路是经乙状窦枕岩入路,无论是单独入路还是与其他入路联合入路,98%的患者实现了大体全切除。术前下颅神经功能正常的患者中,44% (n = 8)出现术后新发麻痹。随访时间12 ~ 144个月,平均63.46个月。肿瘤复发3例(5.6%)。结论:作者根据自己的经验,提出了一种治疗算法,指导最佳手术策略。即使现在可以安全地实现颈静脉孔区病变的大体全肿瘤切除,对该区域的显微外科解剖和手术训练的广泛理解也是必须的。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信
小红书