虚拟计划骨牵引作为治疗Goldenhar综合征所致面肌短小症的金标准

Jeová Clementino Almeida, R. Grillo, R. G. Teixeira
{"title":"虚拟计划骨牵引作为治疗Goldenhar综合征所致面肌短小症的金标准","authors":"Jeová Clementino Almeida, R. Grillo, R. G. Teixeira","doi":"10.1051/mbcb/2022002","DOIUrl":null,"url":null,"abstract":"First described by Von Arlt in 1845, the Goldenhar syndrome was not recognized as an entity until 1952, when the Belgian-American ophthalmologist described the syndrome that bears his name [1]. It has a rare incidence and multifactorial etiology with many prenatal risk factors involved, such as vasoactive drugs, gestational diabetes, twin pregnancies, second trimester bleeding, and artificial reproductive techniques [2]. The syndrome is characterized by peribulbar and/or labial dermoids, atrial appendages and atrial fistulas with a blind bottom located in the pretragus region, microtia and vertebral anomalies [3]. Due to the occurrence of several cases of hemifacial microsomia, this change was considered a distinctive feature of the entity in 1976 [4]. That means the maxillofacial surgeon is under obligation to update and recycle to work with these patients. The syndrome should be diagnosed as soon as possible so the treatment is early and patients do not suffer from physical, psychological, and social developmental delays. Variouc techniques are used in the treatment of hemifacial microsomia, such as bone grafts, customized prosthesis, and bone distraction [5]. The first report on the use of bone distraction in the treatment of hemifacial microsomia in patients with Goldenhar Syndrome dates back to 1996 and is now, after 25 years, it is one of the treatments with considerable acceptance in the literature, although there are not many publications on the subject. Hemifacial microsomia is the second-highest incidence of congenital craniofacial malformations after cleft lip and palate [5].","PeriodicalId":37322,"journal":{"name":"Journal of Oral Medicine and Oral Surgery","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Virtual planning bone distraction as a golden standard in the treatment of hemifacial microsomia due to Goldenhar syndrome\",\"authors\":\"Jeová Clementino Almeida, R. Grillo, R. G. Teixeira\",\"doi\":\"10.1051/mbcb/2022002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"First described by Von Arlt in 1845, the Goldenhar syndrome was not recognized as an entity until 1952, when the Belgian-American ophthalmologist described the syndrome that bears his name [1]. It has a rare incidence and multifactorial etiology with many prenatal risk factors involved, such as vasoactive drugs, gestational diabetes, twin pregnancies, second trimester bleeding, and artificial reproductive techniques [2]. The syndrome is characterized by peribulbar and/or labial dermoids, atrial appendages and atrial fistulas with a blind bottom located in the pretragus region, microtia and vertebral anomalies [3]. Due to the occurrence of several cases of hemifacial microsomia, this change was considered a distinctive feature of the entity in 1976 [4]. That means the maxillofacial surgeon is under obligation to update and recycle to work with these patients. The syndrome should be diagnosed as soon as possible so the treatment is early and patients do not suffer from physical, psychological, and social developmental delays. Variouc techniques are used in the treatment of hemifacial microsomia, such as bone grafts, customized prosthesis, and bone distraction [5]. The first report on the use of bone distraction in the treatment of hemifacial microsomia in patients with Goldenhar Syndrome dates back to 1996 and is now, after 25 years, it is one of the treatments with considerable acceptance in the literature, although there are not many publications on the subject. Hemifacial microsomia is the second-highest incidence of congenital craniofacial malformations after cleft lip and palate [5].\",\"PeriodicalId\":37322,\"journal\":{\"name\":\"Journal of Oral Medicine and Oral Surgery\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Oral Medicine and Oral Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1051/mbcb/2022002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"Dentistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral Medicine and Oral Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1051/mbcb/2022002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Dentistry","Score":null,"Total":0}
引用次数: 1

摘要

1845年冯·阿尔特(Von Arlt)首次描述了戈尔登哈尔综合征,直到1952年,这位比利时裔美国眼科医生描述了以他的名字命名的综合征[1],戈尔登哈尔综合征才被认为是一个实体。该病发病率低,病因多因素,涉及多种产前危险因素,如血管活性药物、妊娠期糖尿病、双胎妊娠、妊娠中期出血和人工生殖技术等。该综合征的特征是球周和/或唇皮样,心房附件和位于耳屏前区盲底的心房瘘,小耳畸形和椎体异常[3]。由于发生了几例面肌短小症,这种变化在1976年被认为是该实体的一个显著特征。这意味着颌面外科医生有义务更新和回收这些病人。该综合征应尽早诊断,以便及早治疗,避免患者出现身体、心理和社会发育迟缓。治疗面肌短小症采用多种技术,如骨移植、定制假体和骨牵引等。关于在Goldenhar综合征患者中使用骨牵引治疗面肌短小症的第一篇报道可以追溯到1996年,25年后的今天,尽管关于该主题的出版物并不多,但它是文献中被广泛接受的治疗方法之一。半面小是继唇裂和腭裂之后发病率第二高的先天性颅面畸形。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Virtual planning bone distraction as a golden standard in the treatment of hemifacial microsomia due to Goldenhar syndrome
First described by Von Arlt in 1845, the Goldenhar syndrome was not recognized as an entity until 1952, when the Belgian-American ophthalmologist described the syndrome that bears his name [1]. It has a rare incidence and multifactorial etiology with many prenatal risk factors involved, such as vasoactive drugs, gestational diabetes, twin pregnancies, second trimester bleeding, and artificial reproductive techniques [2]. The syndrome is characterized by peribulbar and/or labial dermoids, atrial appendages and atrial fistulas with a blind bottom located in the pretragus region, microtia and vertebral anomalies [3]. Due to the occurrence of several cases of hemifacial microsomia, this change was considered a distinctive feature of the entity in 1976 [4]. That means the maxillofacial surgeon is under obligation to update and recycle to work with these patients. The syndrome should be diagnosed as soon as possible so the treatment is early and patients do not suffer from physical, psychological, and social developmental delays. Variouc techniques are used in the treatment of hemifacial microsomia, such as bone grafts, customized prosthesis, and bone distraction [5]. The first report on the use of bone distraction in the treatment of hemifacial microsomia in patients with Goldenhar Syndrome dates back to 1996 and is now, after 25 years, it is one of the treatments with considerable acceptance in the literature, although there are not many publications on the subject. Hemifacial microsomia is the second-highest incidence of congenital craniofacial malformations after cleft lip and palate [5].
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Oral Medicine and Oral Surgery
Journal of Oral Medicine and Oral Surgery Dentistry-Dentistry (miscellaneous)
CiteScore
0.80
自引率
0.00%
发文量
21
审稿时长
24 weeks
期刊最新文献
Acute periapical dental abscesses and increased risk for extracranial carotid artery aneurysms Early lingual nerve suture under local anesthesia after wisdom tooth extraction: a case report The impact of Lidocaine gel on TNF-α expression in surgically induced oral mucosal ulcers: an immunohistochemical analysis in rabbits Management of third molars projected into the temporal fossa and infratemporal fossa: systematic literature review Comparison of buccal based triangular flap and lingual based triangular flap on postoperative course after impacted mandibular third molar surgery: a prospective randomized controlled study
×
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