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Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient

Treacher Collins syndrome is a congenital disorder that is characterized with a wide range of cranio-facial deformities. Zygomatic hypoplasia or aplasia is one of the key features, and surgical reconstruction of the consequent depression on the zygomatic area is deemed necessary by many patients. Va...

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Detalles Bibliográficos
Autores principales: Heo, Jae-Woo, Jin, Ung Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cleft Palate-Craniofacial Association 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057122/
https://www.ncbi.nlm.nih.gov/pubmed/29716177
http://dx.doi.org/10.7181/acfs.2018.01739
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author Heo, Jae-Woo
Jin, Ung Sik
author_facet Heo, Jae-Woo
Jin, Ung Sik
author_sort Heo, Jae-Woo
collection PubMed
description Treacher Collins syndrome is a congenital disorder that is characterized with a wide range of cranio-facial deformities. Zygomatic hypoplasia or aplasia is one of the key features, and surgical reconstruction of the consequent depression on the zygomatic area is deemed necessary by many patients. Various surgical options are available—injectables, alloplastic materials, autologous grafting, and autogenous tissue transfer. It depends on each patient which technique to use. Here, we present a clinical case, in which bilateral free groin flaps were adopted in attempt to resolve the remnant aesthetic deformity associated with zygomatic depression, despite a series of previous surgical efforts, in a 25-year-old Treacher Collins syndrome male patient.
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spelling pubmed-60571222018-07-27 Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient Heo, Jae-Woo Jin, Ung Sik Arch Craniofac Surg Case Report Treacher Collins syndrome is a congenital disorder that is characterized with a wide range of cranio-facial deformities. Zygomatic hypoplasia or aplasia is one of the key features, and surgical reconstruction of the consequent depression on the zygomatic area is deemed necessary by many patients. Various surgical options are available—injectables, alloplastic materials, autologous grafting, and autogenous tissue transfer. It depends on each patient which technique to use. Here, we present a clinical case, in which bilateral free groin flaps were adopted in attempt to resolve the remnant aesthetic deformity associated with zygomatic depression, despite a series of previous surgical efforts, in a 25-year-old Treacher Collins syndrome male patient. Korean Cleft Palate-Craniofacial Association 2018-06 2018-05-03 /pmc/articles/PMC6057122/ /pubmed/29716177 http://dx.doi.org/10.7181/acfs.2018.01739 Text en Copyright © 2018 The Korean Cleft Palate-Craniofacial Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Heo, Jae-Woo
Jin, Ung Sik
Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient
title Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient
title_full Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient
title_fullStr Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient
title_full_unstemmed Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient
title_short Contouring of zygomatic soft tissue using bilateral free groin flaps in a Treacher Collins syndrome patient
title_sort contouring of zygomatic soft tissue using bilateral free groin flaps in a treacher collins syndrome patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057122/
https://www.ncbi.nlm.nih.gov/pubmed/29716177
http://dx.doi.org/10.7181/acfs.2018.01739
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