Anderson Peter J, Netherway David J, Abbott Amanda, Moore Mark, David David J
Australian Craniofacial Unit, Women's and Children's Hospitals, University of Adelaide, South Australia, Australia.
J Craniofac Surg. 2004 Jan;15(1):47-50. doi: 10.1097/00001665-200401000-00015.
Mandibular lengthening by distraction was performed in a 6-year-old severely affected Treacher-Collins syndrome patient who was tracheostomy dependent. As previously reported, this procedure permitted tracheostomy removal once distraction was complete. Now that the patient is skeletally mature, the long-term results of this intervention are reported with regard to his clinical outcome and an assessment of the anatomical changes in the upper airway during growth. Although the distraction could be considered a success in that it enabled permanent decannulation and improved the minimum cross-sectional area of the upper airway, there was no further increase in the minimum cross-sectional area of the upper airway during childhood growth. It is significant that the abnormal growth pattern of the mandible, which is characteristic of this syndrome, did not alter from its preoperative pattern once distraction was completed.
对一名6岁的严重特雷彻-柯林斯综合征患者进行了牵张成骨下颌延长术,该患者依赖气管造口术。如先前报道,一旦牵张完成,该手术允许移除气管造口术。鉴于该患者骨骼已成熟,现报告该干预措施的长期结果,包括其临床结局以及对生长期间上气道解剖学变化的评估。尽管牵张可被视为成功,因为它实现了永久性拔管并改善了上气道的最小横截面积,但在儿童生长期间上气道的最小横截面积没有进一步增加。值得注意的是,这种综合征特有的下颌骨异常生长模式在牵张完成后并未从术前模式改变。