Khonsari Roman H, Way Benjamin, Nysjö Johan, Odri Guillaume A, Olszewski Raphaël, Evans Robert D, Dunaway David J, Nyström Ingela, Britto Jonathan A
The Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom; Assistance Publique - Hôpitaux de Paris, Hôpital Necker Enfants-Malades, Service de Chirurgie Maxillo-faciale et Plastique, Université Paris-Descartes, Paris, France.
The Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
J Craniomaxillofac Surg. 2016 Oct;44(10):1567-1575. doi: 10.1016/j.jcms.2016.08.015. Epub 2016 Aug 21.
A major concern in FGFR2 craniofaciosynostosis is oculo-orbital disproportion, such that orbital malformation provides poor accommodation and support for the orbital contents and peri-orbita, leading to insufficient eyelid closure, corneal exposure and eventually to functional visual impairment. Fronto-facial monobloc osteotomy followed by distraction osteogenesis aims to correct midfacial growth deficiencies in Crouzon-Pfeiffer syndrome patients. Fronto-facial bipartition osteotomy followed by distraction is a procedure of choice in Apert syndrome patients. These procedures modify the shape and volume of the orbit and tend to correct oculo-orbital disproportion. Little is known about the detailed 3D shape of the orbital phenotype in CPS and AS, and about how this is modified by fronto-facial surgery. Twenty-eight patients with CMS, 13 patients with AS and 40 control patients were included. CT scans were performed before and after fronto-facial surgery. Late post-operative scans were available for the Crouzon-Pfeiffer syndrome group. Orbital morphology was investigated using conventional three-dimensional cephalometry and shape analysis after mesh-based segmentation of the orbital contents. We characterized the 3D morphology of CPS and AS orbits and showed how orbital shape is modified by surgery. We showed that monobloc-distraction in CPS and bipartition-distraction in AS specifically address the morphological characteristics of the two syndromes.
FGFR2 相关颅面骨缝早闭的一个主要问题是眼眶比例失调,即眼眶畸形为眼眶内容物和眶周组织提供的容纳和支撑不足,导致眼睑闭合不全、角膜暴露,最终导致功能性视力损害。额面部整块截骨术联合牵引成骨术旨在纠正克鲁宗- Pfeiffer 综合征患者的面中部生长缺陷。额面部二分截骨术联合牵引术是 Apert 综合征患者的首选手术方法。这些手术可改变眼眶的形状和容积,有助于纠正眼眶比例失调。目前对于克鲁宗综合征(CPS)和 Apert 综合征(AS)眼眶表型的详细三维形状,以及额面部手术如何改变这种形状知之甚少。本研究纳入了 28 例 CPS 患者、13 例 AS 患者和 40 例对照患者。在额面部手术前后进行了 CT 扫描。克鲁宗- Pfeiffer 综合征组有术后晚期扫描图像。在基于网格分割眼眶内容物后,采用传统三维头影测量法和形状分析法对眼眶形态进行研究。我们对 CPS 和 AS 眼眶的三维形态进行了特征描述,并展示了手术如何改变眼眶形状。我们发现,CPS 的整块截骨-牵引术和 AS 的二分截骨-牵引术分别针对这两种综合征的形态学特征。