Subtle Manifestation of Lower Cavernous Sinus Syndrome as the Initial and Sole Presentation of Pterygopalatine Squamous Cell Carcinoma Invasion from the Skull Base: A Case Report.

Acta neurologica Taiwanica Pub Date : 2025-07-01 Epub Date: 2025-09-29 DOI:10.4103/ANT.ANT_112_0109
Brian Po-Sheng Wu, Poyin Huang
{"title":"Subtle Manifestation of Lower Cavernous Sinus Syndrome as the Initial and Sole Presentation of Pterygopalatine Squamous Cell Carcinoma Invasion from the Skull Base: A Case Report.","authors":"Brian Po-Sheng Wu, Poyin Huang","doi":"10.4103/ANT.ANT_112_0109","DOIUrl":null,"url":null,"abstract":"<p><p>We present a case highlighting the critical role of early recognition of partial cavernous sinus syndrome (CSS), as diagnostic delay can lead to irreversible tumor progression. A 50-year-old woman presented with subtle binocular diplopia and facial tingling sensation for 1 month. Neurological examination revealed isolated right abducens nerve (VI) palsy and paresthesia at territories of right ophthalmic (V1) and maxillary (V2) nerves. Partial CSS was suspected. Brain magnetic resonance image (MRI) revealed a contrast-enhancing mass involving the pterygopalatine fossa, sphenoid, and maxillary sinuses extending into the cavernous sinus. Fiberscope biopsy confirmed nonkeratinizing squamous cell carcinoma (SCC). After consultation with otolaryngologist, concurrent chemoradiation as the initial treatment modality was suggested. We describe an uncommon etiology of CSS by pterygopalatine SCC invasion, presenting initially as subtle cranial nerve palsies. Involvement of lower anatomical structures in cavernous sinus and \"mandibular sparing\" can be a hint of invasive lesion from pterygopalatine fossa. This case emphasizes the importance of high clinical suspicion for partial CSS, as early recognition can have great impact on patient's prognosis.</p>","PeriodicalId":93852,"journal":{"name":"Acta neurologica Taiwanica","volume":"34 3","pages":"173-175"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta neurologica Taiwanica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ANT.ANT_112_0109","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/29 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

We present a case highlighting the critical role of early recognition of partial cavernous sinus syndrome (CSS), as diagnostic delay can lead to irreversible tumor progression. A 50-year-old woman presented with subtle binocular diplopia and facial tingling sensation for 1 month. Neurological examination revealed isolated right abducens nerve (VI) palsy and paresthesia at territories of right ophthalmic (V1) and maxillary (V2) nerves. Partial CSS was suspected. Brain magnetic resonance image (MRI) revealed a contrast-enhancing mass involving the pterygopalatine fossa, sphenoid, and maxillary sinuses extending into the cavernous sinus. Fiberscope biopsy confirmed nonkeratinizing squamous cell carcinoma (SCC). After consultation with otolaryngologist, concurrent chemoradiation as the initial treatment modality was suggested. We describe an uncommon etiology of CSS by pterygopalatine SCC invasion, presenting initially as subtle cranial nerve palsies. Involvement of lower anatomical structures in cavernous sinus and "mandibular sparing" can be a hint of invasive lesion from pterygopalatine fossa. This case emphasizes the importance of high clinical suspicion for partial CSS, as early recognition can have great impact on patient's prognosis.

下海绵状窦综合征的细微表现是翼腭部鳞状细胞癌从颅底侵入的最初和唯一表现:1例报告。
我们提出一个病例,强调早期识别部分海绵窦综合征(CSS)的关键作用,因为诊断延迟可能导致不可逆转的肿瘤进展。女性,50岁,有轻微双眼复视及面部刺痛感1个月。神经学检查显示孤立性右展神经(VI)麻痹,右眼神经(V1)和上颌神经(V2)区域感觉异常。怀疑存在部分CSS。脑磁共振成像(MRI)显示一个增强肿块累及翼腭窝、蝶窦和上颌窦,并延伸至海绵窦。纤维镜活检证实非角化鳞状细胞癌(SCC)。在与耳鼻喉科医生协商后,建议同步放化疗作为初始治疗方式。我们描述了一个罕见的病因CSS翼腭SCC侵袭,最初表现为细微的脑神经麻痹。海绵窦的下解剖结构受累和“下颌保留”可能提示翼腭窝的侵袭性病变。本病例强调了临床对部分CSS高度怀疑的重要性,因为早期识别对患者预后有很大影响。
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
1.20
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