• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一名成年患者的鼻咽部肿物被诊断为经蝶窦脑膨出。

Nasopharyngeal Mass Diagnosed as Transsphenoidal Encephalocele in an Adult Patient.

作者信息

Ertas Burak, Aksoy Elif Ayanoglu, Unal Omer Faruk

机构信息

*Department of Otorhinolaryngology, Acibadem University, Medical School †Department of Otorhinolaryngology, Koc University, Medical School, Istanbul, Turkey.

出版信息

J Craniofac Surg. 2015 Nov;26(8):e793-4. doi: 10.1097/SCS.0000000000002161.

DOI:10.1097/SCS.0000000000002161
PMID:26595010
Abstract

Transsphenoidal encephalocele, a rare congenital malformation, is generally diagnosed during childhood when investigating the reason for complaints such as nasal obstruction and recurring cerebrospinal fluid fistula. In this adult patient, the authors identified an asymptomatic transsphenoidal encephalocele after requested monitoring of a pedunculated mass detected in the nasopharynx during nasal endoscopy. After evaluation, the authors decided to follow the patient. Few cases of transsphenoidal encephalocele have been reported, and even fewer have been reported in older patients, with no other anomaly or symptoms. The success of surgical treatment for these masses is debatable. The authors did not consider surgery for this asymptomatic case. With this case presentation, the authors wish to emphasize that without making radiologic assessments of any masses identified in a nasopharyngeal examination, it would be inappropriate to perform a biopsy or any intervention.

摘要

经蝶窦脑膨出是一种罕见的先天性畸形,通常在儿童期调查诸如鼻塞和反复脑脊液瘘等主诉原因时被诊断出来。在这位成年患者中,作者在内镜检查时对鼻咽部发现的带蒂肿物进行监测后,发现了一例无症状的经蝶窦脑膨出。经过评估,作者决定对该患者进行随访观察。经蝶窦脑膨出的病例报道较少,在老年患者中且无其他异常或症状的报道更是少之又少。这些肿物手术治疗的成功率存在争议。作者未考虑对这例无症状病例进行手术。通过这例病例报告,作者希望强调,在未对鼻咽部检查中发现的任何肿物进行影像学评估的情况下,进行活检或任何干预都是不合适的。

相似文献

1
Nasopharyngeal Mass Diagnosed as Transsphenoidal Encephalocele in an Adult Patient.一名成年患者的鼻咽部肿物被诊断为经蝶窦脑膨出。
J Craniofac Surg. 2015 Nov;26(8):e793-4. doi: 10.1097/SCS.0000000000002161.
2
Transsellar transsphenoidal encephalocele: a case report.经蝶鞍经蝶骨脑膨出:一例报告。
Pediatr Neurosurg. 2010;46(6):472-4. doi: 10.1159/000325157. Epub 2011 May 10.
3
An unusual cause of nasal airway obstruction in a neonate: trans-sellar, trans-sphenoidal cephalocoele.新生儿鼻气道阻塞的一种罕见原因:经鞍、经蝶骨脑膨出。
J Laryngol Otol. 2011 Oct;125(10):1075-8. doi: 10.1017/S0022215111001800. Epub 2011 Jul 27.
4
Transsphenoidal encephalocele in a neonate.新生儿经蝶骨脑膨出
Ear Nose Throat J. 2006 Jul;85(7):420, 422.
5
Transsphenoidal (large craniopharyngeal) canal associated with a normally functioning pituitary gland and nasopharyngeal extension, hyperprolactinemia, and hypothalamic hamartoma.与功能正常的垂体、鼻咽部延伸、高催乳素血症及下丘脑错构瘤相关的经蝶骨(大型颅咽管)管
AJR Am J Roentgenol. 2003 Jan;180(1):76-7. doi: 10.2214/ajr.180.1.1800076.
6
A rare case of upper airway obstruction in an infant caused by basal encephalocele complicating facial midline deformity.一例罕见的婴儿上呼吸道梗阻病例,由基底脑膨出合并面部中线畸形引起。
Paediatr Anaesth. 1999;9(1):73-6.
7
Trans-sellar trans-sphenoidal encephaloceles: report of two cases.经蝶鞍经蝶骨脑膨出:两例报告。
J Clin Neurosci. 2002 Jan;9(1):89-92. doi: 10.1054/jocn.2001.0861.
8
Transsphenoidal meningoencephalocele in adults.成人经蝶窦脑膜脑膨出
Surg Neurol. 2000 Aug;54(2):183-7; discussion 187-8. doi: 10.1016/s0090-3019(00)00270-6.
9
Transsphenoidal encephalocele masquerading as nasal mass in a 2-year-old boy.一名2岁男孩中伪装成鼻腔肿物的经蝶骨脑膨出。
BMJ Case Rep. 2014 Mar 12;2014:bcr2013201426. doi: 10.1136/bcr-2013-201426.
10
Transsellar transsphenoidal encephalocele: a series of four cases.经蝶窦-颅底脑膨出:系列病例四例。
Neurol India. 2011 Mar-Apr;59(2):289-92. doi: 10.4103/0028-3886.79157.

引用本文的文献

1
A red herring CVA with unexpected outcome: illustrative case.一例结局意外的红鲱鱼样卒中:病例说明
J Neurosurg Case Lessons. 2022 Jan 10;3(2). doi: 10.3171/CASE21565.