Chetty Vaneshri, Haber Samer E, Khonsari Roman Hossein, Arnaud Eric
University of Witwatersrand, CM. Johannesburg General Hospital, South Africa.
Hôpital Necker - Enfants Malades, Assistance Publique - Hôpitaux de Paris, Service de Neurochirurgie Pédiatrique, Unité Fonctionnelle de Chirurgie Crânio-Faciale; Centre de Référence Maladies Rares CRANIOST, Filière Maladies Rares TeteCou; Université de Paris, Université Paris Descartes.
J Craniofac Surg. 2020 May/Jun;31(3):711-715. doi: 10.1097/SCS.0000000000006233.
Children with Apert syndrome have a characteristic inversion of the orientation of the palpebral fissures, an increase of the inter-orbital distance, telecanthus, and exorbitism. Here, Le Fort III osteotomy with subcranial bipartition and distraction osteogenesis was evaluated as a tool to improve the position of the palpebral fissures in Apert syndrome.
All patients with Apert syndrome who underwent Le Fort 3 osteotomy with subcranial bipartition and distraction osteogenesis using an external device, with canthopexy, between 2009 and 2014, with available preoperative and postoperative frontal photographs, were included into the study. Palpebral fissure inclination was measured. Ratios of the intercanthal distance (ICD) to the outer-canthal distance (OCD) and the interpupillary distance to the OCD were computed. Preoperative and postoperative values were compared using the Wilcoxon signed-ranks test.
The authors included 15 patients with Apert syndrome. The mean age at surgery was 10 ± 3.4 years and the average follow-up was 7.3 ± 2.9 years. We found normalization of the negative inclination of the palpebral fissures (right eye: 10.7 ± 2.4 degrees preoperatively versus 7.0 ± 3.1 degrees postoperatively, P < 0.001; left eye: 12.4 ± 3.9 degrees preoperatively versus 8.7 ± 4.1 degrees postoperatively, P = 0.01) and a significant reduction of the inter-pupillary distance: OCD ratio (0.717 ± 0.027 preoperatively versus 0.699 ± 0.030 postoperatively, P = 0.03). These modifications were stable on the long term. There was no significant change of the inter-canthal distance:OCD ratio.
Le Fort III facial advancement with subcranial bipartition and distraction improves the position and orientation of the orbital region in children with Apert syndrome.
患有Apert综合征的儿童具有睑裂方向特征性反转、眶间距增加、内眦赘皮和眼球突出。在此,对采用颅下二分法和牵张成骨的Le Fort III截骨术作为改善Apert综合征患儿睑裂位置的一种手段进行评估。
纳入2009年至2014年间所有接受采用外部装置的颅下二分法和牵张成骨的Le Fort 3截骨术并进行眦固定术且有术前和术后正面照片的Apert综合征患者。测量睑裂倾斜度。计算内眦间距(ICD)与外眦间距(OCD)的比值以及瞳孔间距与OCD的比值。使用Wilcoxon符号秩检验比较术前和术后值。
作者纳入了15例Apert综合征患者。手术时的平均年龄为10±3.4岁,平均随访时间为7.3±2.9年。我们发现睑裂负倾斜度恢复正常(右眼:术前为10.7±2.4度,术后为7.0±3.1度,P<0.001;左眼:术前为12.4±3.9度,术后为8.7±4.1度,P = 0.01),并且瞳孔间距与OCD的比值显著降低(术前为0.717±0.027,术后为0.699±0.030,P = 0.03)。这些改变长期稳定。内眦间距与OCD的比值无显著变化。
采用颅下二分法和牵张的Le Fort III面部前移术可改善Apert综合征患儿眼眶区域的位置和方向。