Ascenço Adriana Sayuri Kurogi, Balbinot Priscilla, Junior Ivan Maluf, D'Oro Ubiratan, Busato Luciano, da Silva Freitas Renato
From the *Hospital de Clínicas, Universidade Federal do Paraná (UFPR); and †Assistance Center for Cleft Lip and Palate (CAIF) of the Secretary of Health, State of Paraná, Curitiba, Brazil.
J Craniofac Surg. 2014 Mar;25(2):352-4. doi: 10.1097/01.scs.0000436741.90536.bf.
Hemifacial microsomia presents with abnormalities including short ramus, absence of condyle, abnormal canting, deviated chin, and facial asymmetry. Many studies about distraction osteogenesis have been published over the last 20 years, but without long-term follow-up. The aim of this study was to evaluate patients with unilateral craniofacial microsomia who were treated with mandible distraction and with follow-up of more than 5 years.
The following retrospective study was evaluated and approved by the Assistance Center for Cleft Lip and Palate. Data were compiled from the charts of 33 patients with hemifacial microsomia who underwent unilateral mandible distraction.
Average age at time of procedure was 7.3 years, with an average degree of distraction of 20 mm. Seventy percent of cases were treated with internal distraction, 30% external. Follow-up varied between 5 and 15 years, with a mean follow-up of 9 years. Ninety percent of the 33 patients in the study had recurrence of their asymmetry. Mean time to postsurgical recurrence was 44 months. Thirty patients were referred for orthognathic surgery. Six patients have already undergone corrective bimaxillary surgery. One patient underwent genioplasty only, and 1 patient underwent genioplasty with orthognathic jaw surgery. Twenty-two patients are awaiting orthognathic surgery, including one with temporomandibular joint ankylosis. Only 3 subjects had good outcomes, without signs of recurrence.
Bone distraction once seemed a promising long-term option for treatment of craniofacial microsomia. However, this has not proven effective for all cases, and most patients needed subsequent orthognathic surgery.
半侧颜面短小畸形表现为包括下颌支短小、髁突缺失、咬合异常、下巴偏斜和面部不对称等异常情况。在过去20年里发表了许多关于牵张成骨术的研究,但均未进行长期随访。本研究的目的是评估接受下颌骨牵张治疗且随访超过5年的单侧颅面短小畸形患者。
以下回顾性研究经唇腭裂援助中心评估并批准。数据来自33例接受单侧下颌骨牵张的半侧颜面短小畸形患者的病历。
手术时的平均年龄为7.3岁,平均牵张程度为20毫米。70%的病例采用内牵张治疗,30%采用外牵张。随访时间为5至15年,平均随访9年。该研究中的33例患者中有90%出现不对称复发。术后复发的平均时间为44个月。30例患者被转诊进行正颌手术。6例患者已经接受了双颌矫正手术。1例患者仅接受了颏成形术,1例患者接受了颏成形术和正颌手术。22例患者正在等待正颌手术,其中1例患有颞下颌关节强直。只有3例患者效果良好,没有复发迹象。
骨牵张术曾一度似乎是治疗颅面短小畸形的一种有前景的长期选择。然而,事实证明这并非对所有病例都有效,大多数患者需要后续的正颌手术。