Bilateral juvenile nasopharyngeal angiofibroma: A rare case report

IF 0.3 Q4 OTORHINOLARYNGOLOGY
M. Adham, Kartika Hajarani, Lisnawati Rachmadi, I. Suroyo
{"title":"Bilateral juvenile nasopharyngeal angiofibroma: A rare case report","authors":"M. Adham, Kartika Hajarani, Lisnawati Rachmadi, I. Suroyo","doi":"10.1080/23772484.2021.1914060","DOIUrl":null,"url":null,"abstract":"Abstract Juvenile nasopharyngeal angiofibroma (JNA) is a benign, vascular, tumour primarily occuring in adolescent males. Juvenile nasopharyngeal angiofibroma is normally unilateral, originating from the sphenopalatine artery. Two separate masses arising from both sides are exceedingly rare. We report a case of a 29-year-old male presented with increasing nasal obstruction, recurrent epistaxis, and a mass on his left buccal. Computed tomography and magnetic resonance imaging revealed non-contiguous tumours on the right nasopharynx and on the left buccal. Angiography showed independent vascular supplies from each side with no bilateral supply noted. Preoperative embolization on both vascular supplies was done, followed by surgical removal of the tumours with no major complication. Histopathological examination showed both are JNA. No major complications were noted. This case discusses how suspecting bilateral juvenile angiofibroma in a patient with two non-contiguous masses in head and neck region is recommended. Proper diagnosis of bilateral JNA can lead to better management and results.","PeriodicalId":40723,"journal":{"name":"Acta Oto-Laryngologica Case Reports","volume":"6 1","pages":"45 - 52"},"PeriodicalIF":0.3000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/23772484.2021.1914060","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Oto-Laryngologica Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/23772484.2021.1914060","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OTORHINOLARYNGOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Abstract Juvenile nasopharyngeal angiofibroma (JNA) is a benign, vascular, tumour primarily occuring in adolescent males. Juvenile nasopharyngeal angiofibroma is normally unilateral, originating from the sphenopalatine artery. Two separate masses arising from both sides are exceedingly rare. We report a case of a 29-year-old male presented with increasing nasal obstruction, recurrent epistaxis, and a mass on his left buccal. Computed tomography and magnetic resonance imaging revealed non-contiguous tumours on the right nasopharynx and on the left buccal. Angiography showed independent vascular supplies from each side with no bilateral supply noted. Preoperative embolization on both vascular supplies was done, followed by surgical removal of the tumours with no major complication. Histopathological examination showed both are JNA. No major complications were noted. This case discusses how suspecting bilateral juvenile angiofibroma in a patient with two non-contiguous masses in head and neck region is recommended. Proper diagnosis of bilateral JNA can lead to better management and results.
双侧青少年鼻咽血管纤维瘤1例
青少年鼻咽血管纤维瘤(JNA)是一种主要发生在青少年男性的良性血管性肿瘤。青少年鼻咽血管纤维瘤通常是单侧的,起源于蝶腭动脉。从两边产生两个独立的质量是极其罕见的。我们报告一个29岁男性的病例表现为鼻塞增加,复发性鼻出血,并在他的左颊肿块。计算机断层扫描和磁共振成像显示在右侧鼻咽部和左侧颊部有不连续的肿瘤。血管造影显示两侧血管独立供应,未见双侧血管供应。术前对两条血管进行栓塞,随后手术切除肿瘤,无重大并发症。组织病理学检查均为JNA。无重大并发症。本病例讨论了在头颈部有两个不相邻肿块的患者如何怀疑双侧青少年血管纤维瘤。正确诊断双侧JNA可获得更好的治疗和效果。
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
9
审稿时长
29 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