Chung Michael T, Levi Benjamin, Hyun Jeong S, Lo David D, Montoro Daniel T, Lisiecki Jeffrey, Bradley James P, Buchman Steven R, Longaker Michael T, Wan Derrick C
Hagey Laboratory for Pediatric Regenerative Medicine, Department of Surgery, Plastic and Reconstructive Surgery Division, Stanford University School of Medicine, Stanford, CA 94305, USA
J Craniofac Surg. 2012 Nov;23(7 Suppl 1):1959-63. doi: 10.1097/SCS.0b013e318258bcf1.
Pierre Robin sequence and Treacher Collins syndrome are both associated with mandibular hypoplasia. It has been hypothesized, however, that the mandible may be differentially affected. The purpose of this study was to therefore compare mandibular morphology in children with Pierre Robin sequence with children with Treacher Collins syndrome using three-dimensional analysis of computed tomographic scans. A retrospective analysis was performed identifying children with Pierre Robin sequence and Treacher Collins syndrome undergoing computed tomography. Three-dimensional reconstruction was performed, and ramus height, mandibular body length, and gonial angle were measured. These were then compared with those in control children with normal mandibles and with the clinical norms corrected for age and sex based on previously published measurements. Mandibular body length was found to be significantly shorter for children with Pierre Robin sequence, whereas ramus height was significantly shorter for children with Treacher Collins syndrome. This resulted in distinctly different ramus height-mandibular body length ratios. In addition, the gonial angle was more obtuse in both the Pierre Robin sequence and Treacher Collins syndrome groups compared with the controls. Three-dimensional mandibular morphometric analysis in patients with Pierre Robin sequence and Treacher Collins syndrome thus revealed distinctly different patterns of mandibular hypoplasia relative to normal controls. These findings underscore distinct considerations that must be made in surgical planning for reconstruction.
皮埃尔·罗宾序列征和特雷彻·柯林斯综合征均与下颌骨发育不全有关。然而,据推测,下颌骨可能受到不同程度的影响。因此,本研究的目的是通过对计算机断层扫描进行三维分析,比较皮埃尔·罗宾序列征患儿和特雷彻·柯林斯综合征患儿的下颌骨形态。对接受计算机断层扫描的皮埃尔·罗宾序列征患儿和特雷彻·柯林斯综合征患儿进行回顾性分析。进行三维重建,并测量升支高度、下颌体长和下颌角。然后将这些测量结果与下颌骨正常的对照儿童以及根据先前发表的测量结果校正了年龄和性别的临床标准进行比较。发现皮埃尔·罗宾序列征患儿的下颌体长明显较短,而特雷彻·柯林斯综合征患儿的升支高度明显较短。这导致升支高度与下颌体长的比例明显不同。此外,与对照组相比,皮埃尔·罗宾序列征组和特雷彻·柯林斯综合征组的下颌角均更为钝角。因此,对皮埃尔·罗宾序列征和特雷彻·柯林斯综合征患者进行的三维下颌骨形态计量分析显示,相对于正常对照组,下颌骨发育不全的模式明显不同。这些发现强调了在重建手术规划中必须考虑的不同因素。