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一名患有克鲁宗综合征的成年患者的面中部前移:改良勒福III型 + 勒福I型截骨术联合颏成形术和鼻背增高术

Midface advancement in an adult patient with Crouzon syndrome: Modified LeFort III + LeFort I osteotomy accompanied by genioplasty and nasal dorsum augmentation.

作者信息

Sh Milad Etemadi, Tajmiri Golnaz

机构信息

Department of Oral and Maxillofacial Surgery, Dental Implants Research Center, Dental Research Institute, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.

Dental Implants Research Center, Dental Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Dent Res J (Isfahan). 2022 Apr 27;19:38. eCollection 2022.

PMID:35669601
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9164669/
Abstract

Crouzon syndrome is an autosomal dominant trait, leading to midface deficiency, undeveloped orbits, short nasal dorsum, and exophthalmos as the typical clinical features. Early correction of craniofacial problems can improve patients' quality of life, but many of these patients with Crouzon syndrome are seeking treatment in older ages when they are missed for multidisciplinary management and distraction technique in proper timing. Modified LeFort III osteotomy is one of the treatment options that can be used for proper resolution in adult patients. The present case report study aims to describe a patient with midface deficiency due to the Crouzon syndrome who has undergone a combination of modified LeFort III osteotomy with the periocular approach and LeFort I osteotomy, nasal dorsum augmentation accompanied by genioplasty, wholly as a single surgical procedure which has been shown that can result in highly satisfactory outcomes for both patient and surgeon.

摘要

克鲁宗综合征是一种常染色体显性性状,典型临床特征为面中部发育不全、眼眶发育不良、鼻背短小和眼球突出。早期矫正颅面问题可改善患者生活质量,但许多克鲁宗综合征患者就诊时年龄较大,错过了多学科管理和适时的牵引技术治疗时机。改良勒福III型截骨术是可用于成年患者恰当矫治的治疗选择之一。本病例报告研究旨在描述一名因克鲁宗综合征导致面中部发育不全的患者,该患者接受了改良勒福III型截骨术联合眼周入路及勒福I型截骨术、鼻背增高术并同期行颏成形术,作为单一手术操作,结果显示对患者和外科医生而言均能取得非常满意的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/96039cea5708/DRJ-19-38-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/e559797c3c43/DRJ-19-38-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/20b31b3b5d54/DRJ-19-38-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/07678d39a639/DRJ-19-38-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/28f1dfba1555/DRJ-19-38-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/96039cea5708/DRJ-19-38-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/e559797c3c43/DRJ-19-38-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/20b31b3b5d54/DRJ-19-38-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/07678d39a639/DRJ-19-38-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/28f1dfba1555/DRJ-19-38-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28dd/9164669/96039cea5708/DRJ-19-38-g005.jpg

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本文引用的文献

1
Patient with Crouzon Syndrome Treated with Modified Le Fort III Osteotomy without Previous Orthodontic Treatment: Case Report and a Review of the Literature.未经正畸治疗采用改良Le Fort III截骨术治疗克鲁宗综合征患者:病例报告及文献综述
Case Rep Dent. 2020 Jan 20;2020:6248971. doi: 10.1155/2020/6248971. eCollection 2020.
2
An Overview of Craniosynostosis Craniofacial Syndromes for Combined Orthodontic and Surgical Management.联合正畸与外科治疗的颅缝早闭颅面综合征概述
Oral Maxillofac Surg Clin North Am. 2020 May;32(2):233-247. doi: 10.1016/j.coms.2020.01.004. Epub 2020 Feb 17.
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Genetic Causes of Craniosynostosis: An Update.
颅缝早闭的遗传病因:最新进展
Mol Syndromol. 2019 Feb;10(1-2):6-23. doi: 10.1159/000492266. Epub 2018 Aug 15.
4
Midface correction in patients with Crouzon syndrome is Le Fort III distraction osteogenesis with a rigid external distraction device the gold standard?颅面骨发育不全综合征患者的中面部矫正采用 Le Fort III 骨切开术联合刚性外牵引器,是金标准吗?
J Craniomaxillofac Surg. 2019 Mar;47(3):420-430. doi: 10.1016/j.jcms.2018.11.028. Epub 2018 Dec 31.
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Qualitative study to identify issues affecting quality of life in adults with craniofacial anomalies.
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Modified Le Fort III osteotomy: A simple solution to severe midfacial hypoplasia.改良 Le Fort III 截骨术:治疗严重面中部发育不全的简单方法。
J Craniomaxillofac Surg. 2018 May;46(5):837-843. doi: 10.1016/j.jcms.2018.03.010. Epub 2018 Mar 21.
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Clinical characteristics of Crouzon syndrome.克鲁宗综合征的临床特征。
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