Orthodontic and surgical management of Goldenhar's syndrome, including joint replacement, orthognathic surgery, and polyetheretherketone implants, using virtual surgical planning

Steven D. Harrison , Reza Movahed , Ryan Semensohn
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引用次数: 0

Abstract

Goldenhar syndrome is a rare syndrome with multiple facial characteristics. These include incomplete development of the ear, nose, soft palate, mandible, maxilla, zygoma, and ocular abnormalities as well. Treatment of these patients requires a multidisciplinary approach involving the orthodontist, craniofacial surgeon, and potentially other specialists. This paper presents a case of Goldenhar's, with detailed treatment objectives which required comprehensive orthodontic care, virtual surgical planning, orthognathic surgery, multipiece maxillary procedure including approximately 14 mm down graft on the affected, right side with an iliac crest bone graft, bilateral temporomandibular joint replacement with advancement of the mandible, polyetheretherketone facial implant for pogonion, on the lower border of the right side of the mandible and right malar area. The treatment outcome reflects a significant improvement in occlusal function, range of movement, and improved facial esthetics, although there is still a 1-2 mm cant of the occlusal plane.
利用虚拟手术规划对戈登哈尔综合征进行正畸和手术治疗,包括关节置换、正颌手术和聚醚醚酮植入物
戈登哈尔综合征是一种罕见的综合征,具有多种面部特征。这些特征包括耳、鼻、软腭、下颌骨、上颌骨、颧骨发育不全,以及眼部异常。这些患者的治疗需要多学科的参与,包括正畸医生、颅颌面外科医生以及可能的其他专家。本文介绍了一例戈登哈尔氏症患者,其详细的治疗目标需要全面的正畸护理、虚拟手术规划、正颌手术、上颌骨多件式手术,包括在受影响的右侧向下移植约 14 毫米的髂嵴骨,进行双侧颞下颌关节置换术并将下颌骨前移,在右侧下颌骨下缘和右侧颊部植入聚醚醚酮面部植入物以治疗息肉。治疗结果表明,虽然咬合平面仍有 1-2 毫米的偏差,但咬合功能、活动范围和面部美观均有明显改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
AJO-DO clinical companion
AJO-DO clinical companion Dentistry, Oral Surgery and Medicine
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审稿时长
73 days
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