Munro I R
Otolaryngol Clin North Am. 1981 Feb;14(1):157-66.
Craniofacial dysplasia is a term covering all types of skeletal anomalies. Craniofacial surgery has made possible the movement of any bone of the face or skull to correct such deformities. Such surgery is a new and separate subspecialty and should be limited to a few regional centers. There are numerous osteotomies available. The common ones are the Le Fort I, II, and III for advancement of different segments of the midface, orbital hypertelorism correction converting each orbit into a box, which moves medially together with the eyeball, and advancement of the forehead to correct premature coronal synostosis in infancy or forehead recession in Crouzon's or Apert's syndrome. In hemifacial microsomia, the asymmetrical skeleton is rotated about the facial midline to produce symmetry, and the mandibular ascending ramus and temporomandibular joint are constructed if absent. Combinations of the various osteotomies are possible, depending upon the type of deformity as assessed by the craniofacial team. Psychosocial study indicates that surgical correction should be undertaken as early as is technically feasible. The four main complications are death, blindness, brain damage, and infection.
颅面发育异常是一个涵盖所有类型骨骼异常的术语。颅面外科手术使得移动面部或颅骨的任何骨骼以矫正此类畸形成为可能。这种手术是一个新的独立亚专业领域,应仅限于少数几个区域中心开展。有多种截骨术可供选择。常见的有用于推进中面部不同节段的勒福Ⅰ型、Ⅱ型和Ⅲ型截骨术,矫正眶距增宽症,即将每个眼眶变成一个盒子,使其与眼球一起向内侧移动,以及推进前额以矫正婴儿期的冠状缝早闭或克鲁宗综合征或阿佩尔综合征中的前额后缩。在半侧颜面短小畸形中,不对称的骨骼围绕面部中线旋转以产生对称,若下颌升支和颞下颌关节缺失则进行重建。根据颅面团队评估的畸形类型,各种截骨术可以组合使用。社会心理研究表明,手术矫正应在技术可行的前提下尽早进行。主要的四种并发症是死亡、失明、脑损伤和感染。