Cargando…

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

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Karampalis, Christos, Bounakis, Nikolaos, Tsirikos, Athanasios I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320598/
https://www.ncbi.nlm.nih.gov/pubmed/25524572
http://dx.doi.org/10.1186/1752-1947-8-446
_version_ 1782356150443835392
author Karampalis, Christos
Bounakis, Nikolaos
Tsirikos, Athanasios I
author_facet Karampalis, Christos
Bounakis, Nikolaos
Tsirikos, Athanasios I
author_sort Karampalis, Christos
collection PubMed
description 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.
format Online
Article
Text
id pubmed-4320598
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-43205982015-02-08 Surgical treatment of scoliosis in Treacher Collins syndrome: a case report Karampalis, Christos Bounakis, Nikolaos Tsirikos, Athanasios I J Med Case Rep Case Report 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. BioMed Central 2014-12-19 /pmc/articles/PMC4320598/ /pubmed/25524572 http://dx.doi.org/10.1186/1752-1947-8-446 Text en © Karampalis et al.; licensee BioMed Central. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Karampalis, Christos
Bounakis, Nikolaos
Tsirikos, Athanasios I
Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
title Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
title_full Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
title_fullStr Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
title_full_unstemmed Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
title_short Surgical treatment of scoliosis in Treacher Collins syndrome: a case report
title_sort surgical treatment of scoliosis in treacher collins syndrome: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4320598/
https://www.ncbi.nlm.nih.gov/pubmed/25524572
http://dx.doi.org/10.1186/1752-1947-8-446
work_keys_str_mv AT karampalischristos surgicaltreatmentofscoliosisintreachercollinssyndromeacasereport
AT bounakisnikolaos surgicaltreatmentofscoliosisintreachercollinssyndromeacasereport
AT tsirikosathanasiosi surgicaltreatmentofscoliosisintreachercollinssyndromeacasereport