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
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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。
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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].
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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
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