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使用Red III设备矫正安特利-比克斯勒综合征患者的面部畸形。

Correction of facial deformity using a Red III device in a patient with Antley-Bixler syndrome.

作者信息

Tunçbilek Gökhan, Vargel Ibrahim, Mavili M Emin

机构信息

Faculty of Medicine, Department of Plastic and Reconstructive Surgery, Hacettepe University, Ankara, Turkey.

出版信息

J Craniofac Surg. 2004 Nov;15(6):1043-8. doi: 10.1097/00001665-200411000-00033.

Abstract

Antley-Bixler syndrome was first described in 1975 and to date at least 44 cases have been reported. In addition to brachycephaly, this syndrome is associated with midface hypoplasia, bilateral radiohumeral synostosis, multiple joint contractures, long bone fractures, dysplastic ears, "pear shaped" nose, and occasionally urogenital or cardiac defects. The authors report a case in a 23-year-old man with severe midface deficiency treated using distraction osteogenesis. A modified Le Fort III osteotomy was performed, and nasal subunit and remaining Le Fort III segment was distracted separately. The classic RED II design was found to be insufficient, so the authors added an extra horizontal bar to the system and converted it to a RED III design. Midface advancement was 11 mm from the porion to the orbitale and 31 mm at point A. Nasal advancement at the nasal root level was 5 mm. There were no complications, and at 4 months after surgery, advancement was stable without any relapse.

摘要

安特利-比克斯勒综合征于1975年首次被描述,迄今为止已报告至少44例。除了短头畸形外,该综合征还与面中部发育不全、双侧桡肱关节融合、多关节挛缩、长骨骨折、发育不良的耳朵、“梨形”鼻子以及偶尔的泌尿生殖系统或心脏缺陷有关。作者报告了1例使用牵引成骨术治疗的23岁严重面中部缺损男性病例。进行了改良的勒福III型截骨术,并分别牵引鼻亚单位和剩余的勒福III型节段。发现经典的RED II设计不够用,因此作者在该系统上增加了一根额外的横杆,并将其转换为RED III设计。面中部从耳点到眶点前移了11毫米,在A点前移了31毫米。鼻根水平的鼻前移为5毫米。无并发症发生,术后4个月时,前移稳定,无任何复发。

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