Munro I R
Can Med Assoc J. 1975 Sep 20;113(6):531-5.
A craniofacial team has been developed to corrdinate the treatment of patients with severe facial deformity and to minimize the surgical risks. Two hundred patients have been evaluated in the last 4 years and more than 100 treated by this team to correct orbital hypertelorism, oxycephaly and plagiocephaly with exophthalmos, features of Crouzon's disease and Apert's and Treacher Collins syndromes, hemifacial microsomia, and severe lower facial deformity and malocclusion. Surgical principles include extensive subperiosteal stripping of bone, osteotomy as necessary, and repositioning maintained by bone grafts. Postoperative evaluation is being maintained for 5 years or to maturity in younger children. Although many of the results are less than perfect, there has been sufficient improvement, especially psychologic and functional, to warrant continuation of the surgical program under closely controlled conditions.
一个颅面治疗团队已经组建起来,以协调严重面部畸形患者的治疗,并将手术风险降至最低。在过去4年里,该团队对200名患者进行了评估,并有100多名患者接受了治疗,以矫正眼眶距过宽、尖头畸形和伴有眼球突出的斜头畸形、克鲁宗病、阿佩尔综合征和特雷彻·柯林斯综合征的特征、半侧颜面短小畸形以及严重的下面部畸形和错牙合。手术原则包括广泛的骨膜下骨剥离、必要时进行截骨术,以及通过骨移植维持重新定位。对年幼儿童的术后评估持续5年或直至其发育成熟。尽管许多结果并不尽善尽美,但已经有了足够的改善,尤其是在心理和功能方面,足以保证在严格控制的条件下继续开展该手术项目。