• 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

[耳廓重复畸形,一种罕见的鳃弓发育障碍]

[Doubling of the pinna, a rare branchial arch developmental disorder].

作者信息

Sauter R, Villavicencio E, Schwager K

机构信息

Department of Surgery, University for Science and Technology, Mbarara, Uganda.

出版信息

Laryngorhinootologie. 2006 Sep;85(9):657-60. doi: 10.1055/s-2006-924987. Epub 2006 Jan 16.

DOI:10.1055/s-2006-924987
PMID:16586278
Abstract

BACKGROUND

Auricular appendices are not unusual, but doubling of the pinna is rare. There is still a controversy if these are derivates from the first or the second branchial arch.

PATIENT

The case of a 3 year old girl is described with doubling of the pinna and hemi facial atrophia. The second pinna was on third of the orthotop regular auricle. It seemed to come from the tragus anlage i. e. originating from the first otic hillock.

RESULTS

The accessory pinna was resected, an aesthetic result could be achieved.

CONCLUSION

Morphology and position of accessory pinnas arise again the question of the origin of the auricular hillocks. This case supports the opinion of Otto that the first hillock only belongs to the first branchial arch and the major part of the auricle is originating from the hillock 2-6 i. e. to the second branchial arch.

摘要

背景

耳廓附件并不罕见,但耳廓重复畸形却很罕见。这些附件是源自第一鳃弓还是第二鳃弓仍存在争议。

患者

描述了一名3岁女孩的病例,其存在耳廓重复畸形和半侧面部萎缩。第二个耳廓位于正常耳廓位置的三分之一处。它似乎起源于耳屏原基,即起源于第一耳丘。

结果

切除了副耳廓,获得了美观的效果。

结论

副耳廓的形态和位置再次引发了耳丘起源的问题。该病例支持奥托的观点,即第一耳丘仅属于第一鳃弓,而耳廓的大部分起源于耳丘2 - 6,即第二鳃弓。

相似文献

1
[Doubling of the pinna, a rare branchial arch developmental disorder].[耳廓重复畸形,一种罕见的鳃弓发育障碍]
Laryngorhinootologie. 2006 Sep;85(9):657-60. doi: 10.1055/s-2006-924987. Epub 2006 Jan 16.
2
Embryology and epidemiology of microtia.小耳畸形的胚胎学与流行病学
Facial Plast Surg. 2009 Aug;25(3):145-8. doi: 10.1055/s-0029-1239444. Epub 2009 Oct 6.
3
Congenital malformations of the external auditory canal.外耳道先天性畸形
Otolaryngol Clin North Am. 1996 Oct;29(5):741-60.
4
[The first and second branchial arch syndrome].[第一、二鳃弓综合征]
Otolaryngol Pol. 1984;38(5):393-9.
5
[External ear duplication, a rare branchial arch abnormality].[外耳重复畸形,一种罕见的鳃弓异常]
Laryngorhinootologie. 2006 Nov;85(11):861.
6
Microtia as an autosomal dominant mutation in a transgenic mouse line: a possible animal model of branchial arch anomalies.耳廓发育不全作为转基因小鼠品系中的常染色体显性突变:一种可能的鳃弓异常动物模型。
Anat Anz. 1991;172(1):1-9.
7
[Branchial arch development in the rat and mouse. I. Development of the sinus cervicalis and operculum].
Acta Anat (Basel). 1981;110(1):7-22.
8
[1st branchial arch syndrome or oro-mandibulo-otic syndrome].
Dent Cadmos. 1984 Nov;52(11):67, 70-1, 73-4 passim.
9
Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome.Eya1在发育中的耳朵和肾脏中的表达:对鳃-耳-肾(BOR)综合征发病机制的理解。
Dev Dyn. 1998 Dec;213(4):486-99. doi: 10.1002/(SICI)1097-0177(199812)213:4<486::AID-AJA13>3.0.CO;2-L.
10
First-and-second--branchial-arch syndrome.
Ear Nose Throat J. 1979 Jun;58(6):261-4.

引用本文的文献

1
The development of the mammalian outer and middle ear.哺乳动物外耳和中耳的发育。
J Anat. 2016 Feb;228(2):217-32. doi: 10.1111/joa.12344. Epub 2015 Jul 30.
2
Reconstruction of middle ear malformations.中耳畸形的重建
GMS Curr Top Otorhinolaryngol Head Neck Surg. 2007;6:Doc01. Epub 2008 Mar 14.