Dumbbell-shaped hypoglossal schwannoma with cystic and hemorrhagic degeneration: A case report of a rare entity

Q4 Medicine
Kaouthar Sfar, Fadwa Jaheddine, Kaoutar Maslouhi, Fatima Chait, Meriem Zhim, Najwa ECH-cherif El Kettani, Meriem Fikri, Mohamed Jiddane, Firdaous Touarsa
{"title":"Dumbbell-shaped hypoglossal schwannoma with cystic and hemorrhagic degeneration: A case report of a rare entity","authors":"Kaouthar Sfar,&nbsp;Fadwa Jaheddine,&nbsp;Kaoutar Maslouhi,&nbsp;Fatima Chait,&nbsp;Meriem Zhim,&nbsp;Najwa ECH-cherif El Kettani,&nbsp;Meriem Fikri,&nbsp;Mohamed Jiddane,&nbsp;Firdaous Touarsa","doi":"10.1016/j.radcr.2025.04.074","DOIUrl":null,"url":null,"abstract":"<div><div>Hypoglossal schwannoma (HS) is a rare, benign tumor arising from the myelin-producing Schwann cells of the twelfth cranial nerve. This tumor typically appears as solid mass, with cystic patterns being extremely rare. A. Kaye classified HS into 3 types based on their origin: type A, completely intracranial; type B, intracranial with extracranial extension via the hypoglossal canal, often referred to as \"dumbbell-shaped\"; and type C, arising solely from the extracranial portion of the XII nerve. Tongue deviation and hypotrophy are the most common symptoms. MRI is the gold standard for accurately characterizing the lesion's features and assessing its relationship with the surrounding structures, while high-resolution CT scan of the skull base is valuable for surgical planning. The treatment of hypoglossal schwannoma (HS) is surgical excision. Advances in microsurgical techniques, radiosurgery and neurophysiological monitoring have significantly reduced mortality and morbidity. Here, we report a case of cystic dumbbell-shaped hypoglossal schwannoma in a 71-year-old woman, aiming to emphasize the clinical and radiological characteristics of this rare entity.</div></div>","PeriodicalId":53472,"journal":{"name":"Radiology Case Reports","volume":"20 8","pages":"Pages 3851-3854"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiology Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1930043325003723","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Hypoglossal schwannoma (HS) is a rare, benign tumor arising from the myelin-producing Schwann cells of the twelfth cranial nerve. This tumor typically appears as solid mass, with cystic patterns being extremely rare. A. Kaye classified HS into 3 types based on their origin: type A, completely intracranial; type B, intracranial with extracranial extension via the hypoglossal canal, often referred to as "dumbbell-shaped"; and type C, arising solely from the extracranial portion of the XII nerve. Tongue deviation and hypotrophy are the most common symptoms. MRI is the gold standard for accurately characterizing the lesion's features and assessing its relationship with the surrounding structures, while high-resolution CT scan of the skull base is valuable for surgical planning. The treatment of hypoglossal schwannoma (HS) is surgical excision. Advances in microsurgical techniques, radiosurgery and neurophysiological monitoring have significantly reduced mortality and morbidity. Here, we report a case of cystic dumbbell-shaped hypoglossal schwannoma in a 71-year-old woman, aiming to emphasize the clinical and radiological characteristics of this rare entity.
哑铃形舌下神经鞘瘤伴囊性及出血性变性:一例罕见病例
舌下神经鞘瘤(HS)是一种罕见的良性肿瘤,起源于第十二脑神经产生髓磷脂的雪旺细胞。该肿瘤典型表现为实性肿块,囊性肿瘤极为罕见。A. Kaye根据起源将HS分为3种类型:A型,完全颅内;B型,颅内经舌下管经颅外延伸,常称为“哑铃形”;C型,仅来自第十二神经的颅外部分。舌偏和萎缩是最常见的症状。MRI是准确表征病变特征和评估其与周围结构关系的金标准,而颅底高分辨率CT扫描对手术计划有价值。舌下神经鞘瘤(HS)的治疗是手术切除。显微外科技术、放射外科和神经生理监测的进步大大降低了死亡率和发病率。在此,我们报告一例71岁女性的囊性哑铃状舌下神经鞘瘤,旨在强调这种罕见实体的临床和放射学特征。
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
Radiology Case Reports
Radiology Case Reports Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.10
自引率
0.00%
发文量
1074
审稿时长
30 days
期刊介绍: The content of this journal is exclusively case reports that feature diagnostic imaging. Categories in which case reports can be placed include the musculoskeletal system, spine, central nervous system, head and neck, cardiovascular, chest, gastrointestinal, genitourinary, multisystem, pediatric, emergency, women''s imaging, oncologic, normal variants, medical devices, foreign bodies, interventional radiology, nuclear medicine, molecular imaging, ultrasonography, imaging artifacts, forensic, anthropological, and medical-legal. Articles must be well-documented and include a review of the appropriate literature.
×
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