Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases

Hemifacial microsomia is the second most common congenital anomaly of the craniofacial region. Hemifacial microsomia is characterised by unilateral hypoplasia of the ear. Treatment of this condition depends on the severity of the lesion. The treatment of hemifacial microsomia must be carried out by...

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Main Authors: Mónica Cano-Rosás, Juan Benito-Cano, Javier Benito-Cano, José María Diosdado-Cano, Pablo Benito-Duque, Adrián Curto
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Clinics and Practice
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Online Access:https://www.mdpi.com/2039-7283/14/6/188
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author Mónica Cano-Rosás
Juan Benito-Cano
Javier Benito-Cano
José María Diosdado-Cano
Pablo Benito-Duque
Adrián Curto
author_facet Mónica Cano-Rosás
Juan Benito-Cano
Javier Benito-Cano
José María Diosdado-Cano
Pablo Benito-Duque
Adrián Curto
author_sort Mónica Cano-Rosás
collection DOAJ
description Hemifacial microsomia is the second most common congenital anomaly of the craniofacial region. Hemifacial microsomia is characterised by unilateral hypoplasia of the ear. Treatment of this condition depends on the severity of the lesion. The treatment of hemifacial microsomia must be carried out by a multidisciplinary group of professionals familiar with this pathology, including plastic surgeons, parapsychologists, orthodontists, and paediatricians. In hemifacial microsomia, microtia is usually accompanied by alterations of the middle ear. Since the ear develops embryonically from the first and second branchial arches, the facial areas that also develop from these embryonic origins are usually affected to a greater or lesser degree, including through hypoplasia of the jaw, maxilla, zygomatic bones, and temporal bone, among others. Although jaw hypoplasia is the most evident deformity in craniofacial microsomia, microtia is the alteration that often has the greatest aesthetic impact on patients. Alterations in dentition are also common, typically presenting as a cephalad inclination of the anterior occlusal plane of the maxilla and mandible on the affected side. This study aims to review the surgical approach and evaluate the results of a paediatric case of hemifacial microsomia. Hemifacial microsomia is present at birth, and successful reconstruction is essential for the correct integration of such infantile patients into society. Multiple facial asymmetries as well as neonatal onset are a challenge for reconstructive surgery, and the importance of multidisciplinary treatment in these patients must be emphasised.
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spelling doaj-art-8d894e5489594139a95a036c8dc9061f2024-12-27T14:18:33ZengMDPI AGClinics and Practice2039-72832024-11-011462410241810.3390/clinpract14060188Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical CasesMónica Cano-Rosás0Juan Benito-Cano1Javier Benito-Cano2José María Diosdado-Cano3Pablo Benito-Duque4Adrián Curto5Department of Surgery, Faculty of Medicine, University of Salamanca, Alfonso X El Sabio Avenue s/n, 37007 Salamanca, SpainPrivate Practice, 28034 Madrid, SpainHelthcare NHS Foundation Trust, Birminghan B7 4BN, UKNewland Dental Care, Lincoln LN1 1YA, UKServicio de Cirugía Plástica y Reparadora del Hospital Ramón y Cajal, 28034 Madrid, SpainDepartment of Surgery, Faculty of Medicine, University of Salamanca, Alfonso X El Sabio Avenue s/n, 37007 Salamanca, SpainHemifacial microsomia is the second most common congenital anomaly of the craniofacial region. Hemifacial microsomia is characterised by unilateral hypoplasia of the ear. Treatment of this condition depends on the severity of the lesion. The treatment of hemifacial microsomia must be carried out by a multidisciplinary group of professionals familiar with this pathology, including plastic surgeons, parapsychologists, orthodontists, and paediatricians. In hemifacial microsomia, microtia is usually accompanied by alterations of the middle ear. Since the ear develops embryonically from the first and second branchial arches, the facial areas that also develop from these embryonic origins are usually affected to a greater or lesser degree, including through hypoplasia of the jaw, maxilla, zygomatic bones, and temporal bone, among others. Although jaw hypoplasia is the most evident deformity in craniofacial microsomia, microtia is the alteration that often has the greatest aesthetic impact on patients. Alterations in dentition are also common, typically presenting as a cephalad inclination of the anterior occlusal plane of the maxilla and mandible on the affected side. This study aims to review the surgical approach and evaluate the results of a paediatric case of hemifacial microsomia. Hemifacial microsomia is present at birth, and successful reconstruction is essential for the correct integration of such infantile patients into society. Multiple facial asymmetries as well as neonatal onset are a challenge for reconstructive surgery, and the importance of multidisciplinary treatment in these patients must be emphasised.https://www.mdpi.com/2039-7283/14/6/188auricular reconstructionhemifacial microsomiamicrotia
spellingShingle Mónica Cano-Rosás
Juan Benito-Cano
Javier Benito-Cano
José María Diosdado-Cano
Pablo Benito-Duque
Adrián Curto
Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases
Clinics and Practice
auricular reconstruction
hemifacial microsomia
microtia
title Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases
title_full Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases
title_fullStr Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases
title_full_unstemmed Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases
title_short Multidisciplinary Treatment of Hemifacial Microsomia: Several Clinical Cases
title_sort multidisciplinary treatment of hemifacial microsomia several clinical cases
topic auricular reconstruction
hemifacial microsomia
microtia
url https://www.mdpi.com/2039-7283/14/6/188
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