• 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

一种新的分类:面神经与内耳畸形相关的异常走行。

A Novel Classification: Anomalous Routes of the Facial Nerve in Relation to Inner Ear Malformations.

机构信息

Department of Otolaryngology, Hacettepe University School of Medicine, Ankara, Turkey.

Department of Otolaryngology, Ondokuz Mayıs University School of Medicine, Samsun, Turkey.

出版信息

Laryngoscope. 2020 Nov;130(11):E696-E703. doi: 10.1002/lary.28596. Epub 2020 Mar 5.

DOI:10.1002/lary.28596
PMID:32134124
Abstract

OBJECTIVES/HYPOTHESIS: The objective of this study was to classify anomalous facial nerve (FN) routes and to determine their association with inner ear malformations (IEMs).

STUDY DESIGN

Retrospective cross sectional study.

METHODS

The computed tomography images of 519 patients (796 ears) with IEMs were retrospectively evaluated, and the abnormal routes of the FN were classified as: Meatal segment: type 1, normal internal auditory canal (IAC); type 2, narrow IAC; type 3, facial canal (FC) only; type 4: separate FC/duplicated IAC. Labyrinthine segment (LS): type 1, normal; type 2a/b/c, mild/moderate/severe anterior displacement; type 3, superior displacement; type 4: straight LS. Tympanic segment (TS): type 1, normal; type 2, superiorly displaced TS; type 3, TS at the oval window; type 4: TS inferior to the oval window; type 5: unclassified. Mastoid segment: type 1, normal facial recess (FR)/normal mastoid segment; type 2: narrow FR; type 3, unclassified.

RESULTS

In meatal segment classification, a narrow IAC was common in ears with cochlear hypoplasia (CH) (76.1%), and only FC was common in ears with severe IEMs (62.7%) such as Michel deformity, common cavity, and cochlear aplasia. Incomplete partition-III has its unique superiorly displaced LS (100%). CH-IV also has its unique mild anterosuperior displacement. Ears with a superiorly displaced TS usually (93.1%) had aplastic or hypoplastic semicircular canals. The FR is likely to be narrow in CH and severe IEMs.

CONCLUSIONS

The FN route is affected in IEMs, which must be kept in mind when operating on ears with IEMs. Especially in CH cases, all segments of the FN can be abnormal.

LEVEL OF EVIDENCE

4 Laryngoscope, 130:E696-E703, 2020.

摘要

目的/假设:本研究的目的是对异常面神经(FN)走行进行分类,并确定其与内耳畸形(IEM)的关系。

研究设计

回顾性横断面研究。

方法

回顾性评估了 519 例(796 耳)IEM 患者的 CT 图像,并将 FN 的异常路径分为:外段:1 型,正常内听道(IAC);2 型,IAC 狭窄;3 型,仅面神经管;4 型:面神经管单独/重复 IAC。迷路段(LS):1 型,正常;2a/b/c 型,轻度/中度/重度前移位;3 型,上移位;4 型:直 LS。鼓室段(TS):1 型,正常;2 型,TS 上移位;3 型,TS 位于卵圆窗;4 型:TS 位于卵圆窗下;5 型:未分类。乳突段:1 型,正常面神经隐窝(FR)/正常乳突段;2 型:FR 狭窄;3 型,未分类。

结果

在外段分类中,耳蜗发育不全(CH)患者的 IAC 狭窄较常见(76.1%),而严重 IEM 患者(如 Michel 畸形、共同腔和耳蜗发育不全)仅面神经管常见(62.7%)。不完全分隔-III 有其独特的上移位 LS(100%)。CH-IV 也有其独特的轻度前上移位。TS 上移位的耳朵通常(93.1%)有发育不良或发育不全的半规管。CH 和严重 IEM 中 FR 可能变窄。

结论

FN 路径在 IEM 中受到影响,在对 IEM 患者进行手术时必须牢记这一点。特别是在 CH 病例中,FN 的所有节段都可能异常。

证据水平

4 级喉镜,130:E696-E703,2020 年。

相似文献

1
A Novel Classification: Anomalous Routes of the Facial Nerve in Relation to Inner Ear Malformations.一种新的分类:面神经与内耳畸形相关的异常走行。
Laryngoscope. 2020 Nov;130(11):E696-E703. doi: 10.1002/lary.28596. Epub 2020 Mar 5.
2
A new classification for cochleovestibular malformations.一种新的耳蜗前庭畸形分类法。
Laryngoscope. 2002 Dec;112(12):2230-41. doi: 10.1097/00005537-200212000-00019.
3
Congenital aplasia of the semicircular canals.先天性半规管发育不全
Otol Neurotol. 2003 May;24(3):437-46. doi: 10.1097/00129492-200305000-00014.
4
[The facial nerve study of multi-slice spiral computed tomography in congenital abnormality of external and middle ear].多层螺旋计算机断层扫描在先天性中耳及外耳畸形中的面神经研究
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2017 Mar 5;31(5):347-351. doi: 10.13201/j.issn.1001-1781.2017.05.005.
5
The vestibulocochlear nerve: aplasia and hypoplasia in combination with inner ear malformations.前庭耳蜗神经:发育不良和发育不全与内耳畸形相结合。
Eur Radiol. 2012 Mar;22(3):519-24. doi: 10.1007/s00330-011-2287-z. Epub 2011 Sep 30.
6
Internal auditory canal volume in normal and malformed inner ears.正常内耳和畸形内耳的内耳道容积。
Eur Arch Otorhinolaryngol. 2023 May;280(5):2149-2154. doi: 10.1007/s00405-022-07676-1. Epub 2022 Oct 9.
7
Variations in the labyrinthine segment of facial nerve canal revealed by high-resolution computed tomography.高分辨率计算机断层扫描显示面神经管迷路段的变异。
Auris Nasus Larynx. 2018 Apr;45(2):261-264. doi: 10.1016/j.anl.2017.05.022. Epub 2017 Aug 10.
8
CT Imaging Categorization and Biomarker Study of Anomalous Tympanic Segment of the Facial Nerves in Patients With Hearing Loss in the Absence of Microtia.无小耳畸形的听力损失患者面神经鼓室段异常的CT成像分类及生物标志物研究
Ear Nose Throat J. 2019 Jul;98(6):340-345. doi: 10.1177/0145561319839899. Epub 2019 Apr 8.
9
Anatomic variations and anomalies involving the facial canal.涉及面神经管的解剖变异和异常。
Otolaryngol Clin North Am. 1991 Jun;24(3):531-53.
10
Histopathology of Inner Ear Malformations: Potential Pitfalls for Cochlear Implantation.内耳畸形的组织病理学:人工耳蜗植入的潜在陷阱。
Otol Neurotol. 2019 Sep;40(8):e839-e846. doi: 10.1097/MAO.0000000000002356.

引用本文的文献

1
The cochlear basal turn as a very preserved region in cochlear hypoplasias: radiological and embryological considerations from a cohort of 125 patients.耳蜗底转作为耳蜗发育不全中一个保存完好的区域:来自125例患者队列的放射学和胚胎学考量
Neuroradiology. 2025 Jun 14. doi: 10.1007/s00234-025-03671-5.
2
Facial Nerve Abnormalities in Congenital Middle Ear Malformations With Comments on Preoperative Detectability: A Report of Two Cases.先天性中耳畸形中的面神经异常及术前可检测性分析:两例报告
Cureus. 2025 Mar 31;17(3):e81488. doi: 10.7759/cureus.81488. eCollection 2025 Mar.
3
Abnormalities of the Facial Nerve in Temporal Bones With Inner Ear Malformations.
内耳畸形颞骨中面神经的异常
Laryngoscope Investig Otolaryngol. 2025 Apr 22;10(2):e70146. doi: 10.1002/lio2.70146. eCollection 2025 Apr.
4
Aberrant Course of the Intratemporal Facial Nerve in Children with Congenital Hearing Loss.先天性听力损失儿童颞内面神经的异常走行
Indian J Otolaryngol Head Neck Surg. 2024 Aug;76(4):3051-3058. doi: 10.1007/s12070-024-04596-w. Epub 2024 Mar 16.
5
Clinical and Radiologic Findings in Children with Anomalous Pontine Cranial Nerves.伴有脑桥脑神经异常的儿童的临床和放射学表现
AJNR Am J Neuroradiol. 2024 Dec 9;45(12):1895-1900. doi: 10.3174/ajnr.A8414.
6
The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear.CHARGE 综合征中的耳蜗畸形谱及 CHD7 基因在内耳胚胎发育中的作用。
Neuroradiology. 2023 Apr;65(4):819-834. doi: 10.1007/s00234-023-03118-9. Epub 2023 Jan 30.
7
Embryology, Malformations, and Rare Diseases of the Cochlea.耳蜗的胚胎学、畸形和罕见疾病。
Laryngorhinootologie. 2021 Apr;100(S 01):S1-S43. doi: 10.1055/a-1349-3824. Epub 2021 Apr 30.
8
Imaging of inner ear malformations: a primer for radiologists.内耳畸形的影像学:放射科医生入门。
Radiol Med. 2021 Oct;126(10):1282-1295. doi: 10.1007/s11547-021-01387-z. Epub 2021 Jul 1.