Woods Roger H, Varma Sanjay, David David J
Adelaide, South Australia, Australia From the Australian Craniofacial Unit, Women's and Children's Hospital.
Plast Reconstr Surg. 2008 Sep;122(3):898-905. doi: 10.1097/PRS.0b013e3181811cb6.
Tessier described rare craniofacial clefts anatomically. The no. 7 cleft is a lateral facial cleft consisting of macrostomia, lateral facial muscular diastasis, and bony abnormalities of the maxilla and zygoma. Early computed tomographic imaging provided preliminary insight into the bony abnormality. This article reviews this patient group, defining the clinical and radiological features, to advise optimal protocol management.
A retrospective case-note review of 15 patients with Tessier no. 7 clefts managed by the Australian Craniofacial Unit over the past 25 years was performed. Cases of hemifacial microsomia and Treacher-Collins syndrome were excluded. Clinical features of the patient group were analyzed with photography (all clefts) and imaging (seven clefts). Surgical management and outcome are reviewed.
Fifteen patients and 18 clefts (three bilateral) were treated during the time period of the study. All patients had macrostomia (mean length, 2 cm) and 94 percent had soft-tissue ridging from muscular diastasis directed toward the tragus (44 percent), temporal area (28 percent), or lateral canthus (22 percent). Bony abnormalities included simple clefting of the maxillary molar region in 55 percent, maxillary duplication in 39 percent, and intermaxillary fusion in 6 percent. Surgical intervention included macrostomia repair at the first available opportunity, resection of maxillary duplication (median age, 4 years), and alveolar bone grafting to the cleft (median age, 10 years). Optimal follow-up of these patients is impaired because of long distances required for review. Patients treated with this management protocol have had good functional and aesthetic results to date.
This article describes the Tessier no. 7 cleft in great detail and suggests a new subclassification of the bony abnormality. An adjusted management protocol is proposed to address the bony abnormalities of cleft and duplication, with favorable outcomes for treated patients with this condition.
泰西埃从解剖学角度描述了罕见的颅面裂。7号裂是一种面部外侧裂,包括巨口症、面部外侧肌肉分离以及上颌骨和颧骨的骨质异常。早期的计算机断层扫描成像对骨质异常提供了初步的认识。本文回顾了这一患者群体,明确其临床和放射学特征,以建议最佳的治疗方案。
对过去25年中由澳大利亚颅面外科治疗的15例泰西埃7号裂患者进行回顾性病例记录分析。排除半侧颜面短小畸形和特雷彻-柯林斯综合征病例。通过摄影(所有裂)和影像学检查(7例裂)分析该患者群体的临床特征。回顾手术治疗方法和结果。
在研究期间共治疗了15例患者和18处裂(3例双侧)。所有患者均有巨口症(平均长度2厘米),94%的患者有因肌肉分离导致的软组织嵴,分别指向耳屏(44%)、颞部区域(28%)或外眦(22%)。骨质异常包括55%的上颌磨牙区单纯裂、39%的上颌重复畸形和6%的上颌间融合。手术干预包括在最早时机修复巨口症、切除上颌重复畸形(中位年龄4岁)以及在裂隙处进行牙槽骨植骨(中位年龄10岁)。由于复查所需路程较远,对这些患者的最佳随访受到影响。采用该治疗方案治疗的患者至今已取得良好的功能和美学效果。
本文详细描述了泰西埃7号裂,并提出了骨质异常的新亚分类。建议调整治疗方案以处理裂隙和重复畸形的骨质异常,对患有这种疾病的患者治疗效果良好。