Skip to main content
Top
Published in: Journal of Medical Case Reports 1/2014

Open Access 01-12-2014 | Case report

Surgical treatment of scoliosis in Treacher Collins syndrome: a case report

Authors: Christos Karampalis, Nikolaos Bounakis, Athanasios I Tsirikos

Published in: Journal of Medical Case Reports | Issue 1/2014

Login to get access

Abstract

Introduction

Treacher Collins syndrome is an autosomal dominant disorder resulting in congenital craniofacial deformities. Scoliosis has not been previously reported as one of the extracranial manifestations of this syndromic condition.

Case presentation

We present a 15-year-old British Caucasian girl with Treacher Collins syndrome who developed a severe double thoracic scoliosis measuring 102° and 63° respectively. The deformity was noted at age 14 years by the local general practitioner and gradually progressed until she was referred to our service and subsequently was scheduled for surgical correction. There were no congenital vertebral anomalies. As part of the condition, she had bilateral conductive hearing impairment. She also had reduced respiratory reserves and a restrictive lung disease. Both curves were rigid on supine maximum traction radiographs. She underwent a single-stage anterior and posterior spinal arthrodesis with pedicle hook/sublaminar wire/screw and rod instrumentation and autologous rib graft, supplemented by allograft bone and made a good postoperative recovery. Her scoliosis was corrected to 25° and 24° and a balanced spine in the coronal and sagittal planes was achieved. At latest follow-up beyond skeletal maturity (3 years post-surgery) she had an excellent cosmetic outcome with no loss of deformity correction, no detected pseudarthrosis and a normal level of activities.

Conclusions

Scoliosis can occur in patients with Treacher Collins syndrome with the deformity demonstrating significant deterioration around the adolescent growth spurt. A high index of awareness will allow for an early diagnosis and scoliosis correction at a stage when this can be safer and performed through a single-stage posterior procedure. If the deformity is detected at a later age and stage of growth as occurred in our patient, more complex surgery is required and this increases the risk for major morbidity and potential mortality. Surgical treatment can correct the deformity, balance the spine and restore cosmesis, as well as prevent mechanical back pain and respiratory complications if the scoliosis progressed to cause severe thoracic distortion. A thorough preoperative assessment can diagnose associated comorbidities and reduce the risk for postoperative complications.
Appendix
Available only for authorised users
Literature
1.
go back to reference Dixon MJ: Treacher Collins syndrome. Hum Molec Genet. 1996, 5: 1391-1396.PubMed Dixon MJ: Treacher Collins syndrome. Hum Molec Genet. 1996, 5: 1391-1396.PubMed
2.
go back to reference Dauwerse JG, Dixon J, Seland S, Ruivenkamp CA, van Haeringen A, Hoefsloot LH, Peters DJ, Boers AC, Daumer-Haas C, Maiwald R, Zweier C, Kerr B, Cobo AM, Toral JF, Hoogeboom AJ, Lohmann DR, Hehr U, Dixon MJ, Breuning MH, Wieczorek D: Mutations in gene encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genet. 2011, 43: 20-22. 10.1038/ng.724.CrossRefPubMed Dauwerse JG, Dixon J, Seland S, Ruivenkamp CA, van Haeringen A, Hoefsloot LH, Peters DJ, Boers AC, Daumer-Haas C, Maiwald R, Zweier C, Kerr B, Cobo AM, Toral JF, Hoogeboom AJ, Lohmann DR, Hehr U, Dixon MJ, Breuning MH, Wieczorek D: Mutations in gene encoding subunits of RNA polymerases I and III cause Treacher Collins syndrome. Nature Genet. 2011, 43: 20-22. 10.1038/ng.724.CrossRefPubMed
4.
go back to reference Scully C, Langdon J, Evans J: Marathon of eponyms: 20 Treacher Collins syndrome. Oral Dis. 2011, 17 (6): 619-620. 10.1111/j.1601-0825.2009.01552.x.CrossRefPubMed Scully C, Langdon J, Evans J: Marathon of eponyms: 20 Treacher Collins syndrome. Oral Dis. 2011, 17 (6): 619-620. 10.1111/j.1601-0825.2009.01552.x.CrossRefPubMed
5.
go back to reference Collins ET: Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones. Trans Ophthalmol Soc U K. 1900, 20: 190-192. Collins ET: Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones. Trans Ophthalmol Soc U K. 1900, 20: 190-192.
6.
go back to reference Franceschetti A, Klein D: The mandibulofacial dysostosis; a new hereditary syndrome. Acta Ophthalmol (Copenh). 1949, 27 (2): 143-224. Franceschetti A, Klein D: The mandibulofacial dysostosis; a new hereditary syndrome. Acta Ophthalmol (Copenh). 1949, 27 (2): 143-224.
8.
go back to reference Ochi H, Matsubara K, Ito M, Kusanagi Y: Prenatal sonographic diagnosis of Treacher Collins syndrome. Obstet Gynecol. 1998, 91 (5 Pt 2): 862-PubMed Ochi H, Matsubara K, Ito M, Kusanagi Y: Prenatal sonographic diagnosis of Treacher Collins syndrome. Obstet Gynecol. 1998, 91 (5 Pt 2): 862-PubMed
9.
go back to reference Crane JP, Beaver HA: Midtrimester sonographic diagnosis of mandibulofacial dysostosis. Am J Med Genet. 1986, 25: 251-255. 10.1002/ajmg.1320250209.CrossRefPubMed Crane JP, Beaver HA: Midtrimester sonographic diagnosis of mandibulofacial dysostosis. Am J Med Genet. 1986, 25: 251-255. 10.1002/ajmg.1320250209.CrossRefPubMed
10.
go back to reference Terner JS, Travieso R, Chang C, Bartlett SP, Steinbacher DM: An analysis of mandibular volume in Treacher Collins syndrome. Plast Reconstr Surg. 2012, 129 (4): 751e-753e. 10.1097/PRS.0b013e318245e903.CrossRefPubMed Terner JS, Travieso R, Chang C, Bartlett SP, Steinbacher DM: An analysis of mandibular volume in Treacher Collins syndrome. Plast Reconstr Surg. 2012, 129 (4): 751e-753e. 10.1097/PRS.0b013e318245e903.CrossRefPubMed
11.
go back to reference Hansen M, Lucarelli MJ, Whiteman DAH, Mulliken JB: Treacher Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomas. Am J Med Genet. 1996, 61: 71-74. 10.1002/(SICI)1096-8628(19960102)61:1<71::AID-AJMG14>3.0.CO;2-T.CrossRefPubMed Hansen M, Lucarelli MJ, Whiteman DAH, Mulliken JB: Treacher Collins syndrome: phenotypic variability in a family including an infant with arhinia and uveal colobomas. Am J Med Genet. 1996, 61: 71-74. 10.1002/(SICI)1096-8628(19960102)61:1<71::AID-AJMG14>3.0.CO;2-T.CrossRefPubMed
12.
go back to reference Li C, Mernagh J, Bourgeois J: Novel craniofacial and extracraniofacial findings in a case of Treacher Collins syndrome with a pathogenic mutation and a missense variant in the TCOF1 gene. Clin Dysmorph. 2009, 18: 63-68. 10.1097/MCD.0b013e328318c4fb.CrossRefPubMed Li C, Mernagh J, Bourgeois J: Novel craniofacial and extracraniofacial findings in a case of Treacher Collins syndrome with a pathogenic mutation and a missense variant in the TCOF1 gene. Clin Dysmorph. 2009, 18: 63-68. 10.1097/MCD.0b013e328318c4fb.CrossRefPubMed
Metadata
Title
Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
Authors
Christos Karampalis
Nikolaos Bounakis
Athanasios I Tsirikos
Publication date
01-12-2014
Publisher
BioMed Central
Published in
Journal of Medical Case Reports / Issue 1/2014
Electronic ISSN: 1752-1947
DOI
https://doi.org/10.1186/1752-1947-8-446

Other articles of this Issue 1/2014

Journal of Medical Case Reports 1/2014 Go to the issue