Nasal reconstruction in a rare case of unilateral arhinia in bosma arhinia microphthalmia syndrome

IF 0.1 Q4 SURGERY Turkish Journal of Plastic Surgery Pub Date : 2024-01-01 DOI:10.4103/tjps.tjps_53_23
K. Agrawal, Armaan Khosa, Vidhi Mehta, Vinita Puri
{"title":"Nasal reconstruction in a rare case of unilateral arhinia in bosma arhinia microphthalmia syndrome","authors":"K. Agrawal, Armaan Khosa, Vidhi Mehta, Vinita Puri","doi":"10.4103/tjps.tjps_53_23","DOIUrl":null,"url":null,"abstract":"Bosma arhinia microphthalmia (BAM) is a very rare illness, with fewer than 100 cases documented worldwide. Criteria for diagnosis of BAM syndrome include congenital absence of nose (arhinia) or hypoplasia, hypogonadotropic hypogonadism, and eye defects (microphthalmia) in males. Our patient was a male child of 4 years of age who was brought by parents with left nasal arhinia for reconstruction. We devised three-layered nasal reconstruction for the child. Flip-over flap from the other half of the nose was used for the nasal lining, conchal cartilage grafts for the nasal framework, and pedicled forehead flap for skin cover.","PeriodicalId":42065,"journal":{"name":"Turkish Journal of Plastic Surgery","volume":null,"pages":null},"PeriodicalIF":0.1000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Plastic Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/tjps.tjps_53_23","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"SURGERY","Score":null,"Total":0}
引用次数: 0

Abstract

Bosma arhinia microphthalmia (BAM) is a very rare illness, with fewer than 100 cases documented worldwide. Criteria for diagnosis of BAM syndrome include congenital absence of nose (arhinia) or hypoplasia, hypogonadotropic hypogonadism, and eye defects (microphthalmia) in males. Our patient was a male child of 4 years of age who was brought by parents with left nasal arhinia for reconstruction. We devised three-layered nasal reconstruction for the child. Flip-over flap from the other half of the nose was used for the nasal lining, conchal cartilage grafts for the nasal framework, and pedicled forehead flap for skin cover.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
一例罕见的单侧鼻泪管小眼综合征病例的鼻重建手术
博斯玛鼻炎小眼症(BAM)是一种非常罕见的疾病,全世界记录在案的病例不到 100 例。BAM综合征的诊断标准包括男性先天性无鼻(鼻缺失)或鼻发育不良、性腺功能低下和眼部缺陷(小眼球症)。我们的患者是一名 4 岁男童,父母带他来进行左鼻重建。我们为患儿设计了三层鼻重建手术。使用另一半鼻翼的翻转皮瓣作为鼻腔内衬,使用耳廓软骨移植作为鼻腔框架,使用前额脚皮瓣作为皮肤覆盖。
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 去求助
来源期刊
CiteScore
0.50
自引率
0.00%
发文量
8
审稿时长
28 weeks
期刊最新文献
Glomus tumors of the digit: A retrospective analysis of clinical and functional outcomes The effect of deferoxamine on fat graft survival in tamoxifen use: An experimental study Nasal reconstruction in a rare case of unilateral arhinia in bosma arhinia microphthalmia syndrome A complication after radiofrequency ablation: Skin necrosis Comparative analysis of speech outcomes in the treatment of velopharyngeal insufficiency: Traditional superior-based pharyngeal flap and pharyngeal flap combined with radical intravelar veloplasty
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1