先天性髁突畸形的病因及治疗方法

doi:10.13591/j.cnki.kqyx.2022.08.014

Abstract

Abstract: Congenital condyle deformity is a common manifestation in the first and second branchial arch syndrome. The clinical feature, surgical treatment and prognosis of this syndrome have been reported by a few studies. Understanding the etiology and treatment of congenital condyle deformities is conducive to its prevention, diagnosis, improving postoperative outcomes and mental health of patients, even providing better operation conditions for orthognathic surgery. This article briefly reviews discussions on the etiology and treatment of congenital condyle deformity, in order to provide reference for clinical diagnosis and treatment planning.

Key words: condyle deformity, the first and second branchial arch syndrome, condyle reconstruction, distraction osteogenesis

CLC Number:

R782.23

DING Yu, YU Lüfeng, ZOU Derong. The cause and treatment of congenital condyle deformity[J]. Stomatology, 2022, 42(8): 745-749.

References

[1] Shakir S, Bartlett SP. Modern mandibular distraction applications in hemifacial microsomia[J]. Clin Plast Surg, 2021, 48(3):375-389.
[2] Romanelli Tavares VL, Zechi-Ceide RM, Bertola DR, et al. Targeted molecular investigation in patients within the clinical spectrum of Auriculocondylar syndrome[J]. Am J Med Genet A, 2017, 173(4):938-945.
[3] 郝瑾, 刘争, 孔维佳, 等. Treacher Collins综合征病例报告及文献复习[J]. 临床耳鼻咽喉科杂志, 2006, 20(13):582-584.
[4] Peck CJ, Lopez J, Smetona JT, et al. Treacher collins mandibular distraction[J]. Clin Plast Surg, 2021, 48(3):431-444.
[5] Trindade PAK, Bueno PM, Scomparin L, et al. The role of double-step advancement genioplasty and bilateral coronoidectomy in Nager Syndrome:A case report[J]. Spec Care Dentist, 2021:scd.12585.
[6] 许和平, 林广民, 郭炜然. 桡骨缺陷伴半面短小征(Nager综合征)一例[J]. 中华整形外科杂志, 2008, 24(6):484-485.
[7] vonMarttens A, Perilla A, Wen S, et al. Implant-supported maxillary and mandibular rehabilitation in a patient with hallermann-streiff syndrome[J]. J Craniofac Surg, 2021, 32(1):e20-e23.
[8] 王卫. Hallermann-Streiff综合征-附2例报告[J]. 中国优生与遗传杂志, 1995,3(4):104-105.
[9] Hassani A, Mahaseni Aghdam H, Fazel S, et al. Oculo-auriculo-vertebral spectrum with complete absence of the right condyle and ramus-Case report[J]. Hum Pathol:Case Rep, 2019, 15:50-53.
[10] Meazzini MC, Brusati R, Caprioglio A, et al. True hemifacial microsomia and hemimandibular hypoplasia with condylar-coronoid collapse:Diagnostic and prognostic differences[J]. Am J Orthod Dentofac Orthop, 2011, 139(5):e435-e447. DOI:10.1016/j.ajodo.2010.01.034.
[11] 杨亦楠, 唐晓军, 张智勇, 等. 耳髁突综合征下颌畸形及面部轮廓矫正的综合治疗[J]. 中华整形外科杂志, 2018, 34(4):279-283.
[12] 梁琼鹤, 管红梅, 韩素芳, 等. 婴幼儿Treacher Collins综合征的CT表现[J]. 中国临床医学影像杂志, 2018, 29(10):729-733.
[13] Cadieux-Dion M, Hughes S, Engleman K, et al. Nager syndrome in patient lacking acrofacial dysostosis:Expanding the phenotypic spectrum of SF3B4-related disease[J]. Am J Med Genet Part A, 2021, 185(5):1515-1518.
[14] Kargapolova Y, Rehimi R, Kayserili H, et al. Overarching control of autophagy and DNA damage response by CHD6 revealed by modeling a rare human pathology[J]. Nat Commun, 2021, 12(1):3014.
[15] Innes AM, Lynch DC. Fifty years of recognizable patterns of human malformation:Insights andopportunities[J]. Am J Med Genet A, 2021, 185(9):2653-2669.
[16] Jahanimoghadam F, Sharifi M. Goldenhar syndrome in a 6-year-old patient:A case report and review of literature[J]. J Dent (Shiraz), 2019, 20(4):298-303.
[17] Tingaud-Sequeira A, Trimouille A, Salaria M, et al. A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum[J]. Hum Genet, 2021, 140(6):933-944.
[18] Perrotta S, Bocchino T, D'Antò V, et al. Pseudo hemifacial microsomia with condylar-coronoid collapse:New therapeutic approach in growing patients[J]. J Craniofac Surg, 2020, 31(8):2128-2131.
[19] 相磊, 李永锋, 刘华蔚, 等. 胚胎期颞下颌关节发育相关信号分子与转录因子研究进展[J]. 中华口腔医学杂志, 2021, 56(8):805-809.
[20] 张晔, 潘博. Nager综合征的研究现状[J]. 医学综述, 2015, 21(10):1839-1842.
[21] Chen CL, Peng J, Jia XG, et al. Hallermann-Streiff syndrome with bilateral microphthalmia, pupillary membranes and cataract absorption[J]. Int J Ophthalmol, 2017, 10(6):1016-1018.
[22] Li J, Peng D, Jiang T, et al. Satoyoshi syndrome with progressive orofacial manifestations:A case history report[J]. Int J Prosthodont, 2017, 30(2):163-167.
[23] Zarour CC, Robinson C, Mian A, et al. Idiopathic mandibular condyle resorption[J]. Cureus, 2020:11365.
[24] 胥曦. 儿童严重半侧颜面短小畸形颌骨形态特点分析及治疗策略的研究[D]. 北京:北京协和医学院, 2020.
[25] 刘瑜, 岑瑛, 李正勇. 半侧颜面短小畸形现代医学研究和治疗进展[J]. 华西医学, 2021, 36(2):265-270.
[26] Paul MA, Opyrchał J, Knakiewicz M, et al. Hemifacial microsomia review:Recent advancements in understanding the disease[J]. J Craniofacial Surg, 2020, 31(8):2123-2127.
[27] Emodi O, Israel Y, Almos ME, et al. Three-dimensional planning and reconstruction of the mandible in children with craniofacial microsomia type Ⅲ using costochondral grafts[J]. Ann Maxillofac Surg, 2017, 7(1):64-72.
[28] 马绪臣.颞下颌关节病的基础与临床[M]. 北京:人民出版社, 2004:361-362.
[29] Yang JH, Suh SW, Chang DG. Rib regeneration morphology after thoracoplasty in adolescent idiopathic scoliosis[J]. Spine (Phila Pa 1976), 2020, 45(3):177-183.
[30] Shahzad F. Pediatric mandible reconstruction:Controversies and considerations[J]. Plast Reconstr Surg Glob Open, 2020, 8(12):e3285.
[31] Rikhotso RE, Sekhoto MG. Alloplastic total temporomandibular joint reconstruction:A 10-year experience of the university of the Witwatersrand, Johannesburg[J]. J Craniofac Surg, 2021, 32(5):1658-1663.
[32] Sinn DP,Tandon R, Tiwana PS. Can alloplastic total temporomandibular joint reconstruction be used in the growing patient? A preliminary report[J]. J Oral Maxillofac Surg, 2021, 79(11):2267.e1-2267.e16.
[33] Vanesa V, Irene MP, Marta AS, et al. Accuracy of virtually planned mandibular distraction in a pediatric case series[J]. J Cranio-Maxillofac Surg, 2021, 49(2):154-165.
[34] Anderson SR, Pak KY, Vincent AG, et al. Reconstruction of the mandibular condyle[J]. Facial Plastic Surg, 2021:541-546.
[35] 刘山春. 儿童半侧颜面短小牵张成骨联合固定期牙合板对下颌骨形态的影响[D]. 北京:北京协和医学院, 2018.
[36] Morris R, Beckett J, Steinbacher DM. Simultaneous costochondral ramus-condyle reconstruction and mandibular distraction for hemifacial microsomia[J]. J Oral Maxillofac Surg, 2012, 70(10):e541-e546.
[37] Guo PP, Pan B, Jiang HY, et al. Prevention methods for Treacher Collins syndrome:A systematic review[J]. Int J Pediatr Otorhinolaryngol, 2020, 134:110062.
[38] Apolloni F, De Leonardis L, Sagron M, et al. Mandible customized distraction osteogenesis in Treacher Collins patient:Literature review, report of a case and post-distraction analysis[J]. Interdiscip Neurosurg, 2020, 21:100761.
[39] 柳稚旭, 王旭东, 孙昊. 第一二鳃弓综合征患者下牙槽神经解剖与Pruzansky分类相关性研究[C]//第十四次中国口腔颌面外科学术会议论文集. 重庆, 2018:662-663.
[40] Flannery KM, Yu JW,Resnick CM, et al. Bradycardia and asystole during temporomandibular joint reconstruction[J]. Paediatr Anaesth, 2020, 30(10):1146-1148.
[41] Reighard CL, Powell AR, Zurawski TY, et al. Development of a novel mandibular distraction osteogenesis simulator using Computer Aided Design and 3D printing[J]. Int J Pediatr Otorhinolaryngol, 2021, 142:110616.
[42] Igelbrink S, Zanettini LMS, Bohner L, et al. Three-dimensional planning of the mandibular margin in hemifacial microsomia using a printed patient-specific implant[J]. J Craniofac Surg, 2020, 31(8):2297-2301.

The cause and treatment of congenital condyle deformity

PDF (PC)

Knowledge

Abstract

Cite this article

share this article

References

Related Articles 3

Recommended Articles

Metrics

Comments

[1]	. The role of lateral pterygoid muscle in traumatic temporomandibular joint ankylosis [J]. , 2018, 38(3): 211-216.
[2]	. Research progress of the accelerated distal movement of canine by periodontal ligament distraction osteogenesis [J]. , 2017, 37(12): 1135-1138.
[3]	. Experimental study of mandibular distraction osteogenesis with titanium membrane as the transition disc [J]. , 2014, 34(7): 497-499.