首页> 外文期刊>The Journal of craniofacial surgery >Posterior vault distraction with midface distraction without osteotomy as a first stage for syndromic craniosynostosis
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Posterior vault distraction with midface distraction without osteotomy as a first stage for syndromic craniosynostosis

机译:后穹ault牵开,中脸撑开,无截骨术是综合征性颅骨前突综合征的第一阶段

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Syndromic craniosynostosis (SC) may cause intracranial hypertension, exorbitism, midfacial hypoplasia associated with airway obstruction, and class III malocclusion. Current treatment strategies for SC involve expansion of the cranial vault and orbits, and midfacial advancement to relieve symptoms and sequelae of obstructive sleep apnea. We present a case of a 12-week-old female patient with Saethre-Chotzen syndrome who presented with bicoronal craniosynostosis, severe turribrachycephaly, midface hypoplasia, and a history of obstructive sleep apnea (apnea-hypopnea index = 14). Posterior vault distraction and simultaneous transfacial pin placement under 3D CT surgical navigation was planned to concurrently relieve intracranial pressure and address airway obstruction by distraction of the midface without osteotomy.An uncomplicated surgery was completed in 290 minutes with an estimated blood loss of 340 mL. Midface distraction was initiated on postoperative day 1 at a rate of 1 mm per day for 21 days, which translated to 13 mm of midfacial advancement. Posterior vault distraction was initiated on postoperative day 5 at a rate of 1 mm per day for 25 days with a resultant 25 mm of posterior vault expansion. Transfacial pin and external distractors were removed after 6 weeks, and posterior vault distractors were removed after 8 weeks of consolidation. Craniometric comparison of 3D-CT scan demonstrated an increase in cranial vault volume of 47%, and the patient was able to be weaned from her home oxygen requirement. This is the first report of simultaneous posterior vault distraction with midfacial advancement across open facial sutures using surgical navigation as an initial stage in treating syndromic craniosynostosis.
机译:综合征性颅骨前突合并症(SC)可能引起颅内高压,眶外压,与气道阻塞相关的面中发育不全和III类错牙合。当前SC的治疗策略包括扩大颅穹顶和眼眶,以及促进颌面进展以缓解阻塞性睡眠呼吸暂停的症状和后遗症。我们介绍了一个12周龄的Saethre-Chotzen综合征女性患者,该患者表现为双冠状颅突性鼻窦炎,严重的头颅前突,中面部发育不全和阻塞性睡眠呼吸暂停史(呼吸暂停-低通气指数= 14)。计划在3D CT手术导航下进行后穹dis牵张和同时经面置入针头,以通过不带截骨术的中脸牵张同时缓解颅内压并解决气道阻塞.290分钟内完成了简单的手术,估计失血340毫升。术后第1天以每天1毫米的速度开始21分的脸中部牵引,转化为13毫米的中颌前移。术后第5天以每天1mm的速度开始后穹dis牵引,持续25天,结果后穹expansion扩张25mm。 6周后去除经销和外牵引器,巩固8周后去除后穹dis牵引器。 3D-CT扫描的颅骨测量法比较显示颅穹volume体积增加了47%,并且该患者能够从家中的氧气需求中摆脱出来。这是关于使用手术导航作为治疗综合征性颅前突的初始阶段同时进行后穹ault牵张和面颊跨开放缝线前进的报道。

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