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Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series
Objectives. First branchial cleft anomalies (BCAs) constitute a rare entity with variable clinical presentations and anatomic findings. Given the high rate of recurrence with incomplete excision, identification of the entire tract during surgical treatment is of paramount importance. The objectives...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789415/ https://www.ncbi.nlm.nih.gov/pubmed/27034873 http://dx.doi.org/10.1155/2016/3902974 |
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author | Quintanilla-Dieck, Lourdes Virgin, Frank Wootten, Chistopher Goudy, Steven Penn, Edward |
author_facet | Quintanilla-Dieck, Lourdes Virgin, Frank Wootten, Chistopher Goudy, Steven Penn, Edward |
author_sort | Quintanilla-Dieck, Lourdes |
collection | PubMed |
description | Objectives. First branchial cleft anomalies (BCAs) constitute a rare entity with variable clinical presentations and anatomic findings. Given the high rate of recurrence with incomplete excision, identification of the entire tract during surgical treatment is of paramount importance. The objectives of this paper were to present five anatomic variations of first BCAs and describe the presentation, evaluation, and surgical approach to each one. Methods. A retrospective case review and literature review were performed. We describe patient characteristics, presentation, evaluation, and surgical approach of five patients with first BCAs. Results. Age at definitive surgical treatment ranged from 8 months to 7 years. Various clinical presentations were encountered, some of which were atypical for first BCAs. All had preoperative imaging demonstrating the tract. Four surgical approaches required a superficial parotidectomy with identification of the facial nerve, one of which revealed an aberrant facial nerve. In one case the tract was found to travel into the angle of the mandible, terminating as a mandibular cyst. This required en bloc excision that included the lateral cortex of the mandible. Conclusions. First BCAs have variable presentations. Complete surgical excision can be challenging. Therefore, careful preoperative planning and the recognition of atypical variants during surgery are essential. |
format | Online Article Text |
id | pubmed-4789415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47894152016-03-31 Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series Quintanilla-Dieck, Lourdes Virgin, Frank Wootten, Chistopher Goudy, Steven Penn, Edward Case Rep Otolaryngol Case Report Objectives. First branchial cleft anomalies (BCAs) constitute a rare entity with variable clinical presentations and anatomic findings. Given the high rate of recurrence with incomplete excision, identification of the entire tract during surgical treatment is of paramount importance. The objectives of this paper were to present five anatomic variations of first BCAs and describe the presentation, evaluation, and surgical approach to each one. Methods. A retrospective case review and literature review were performed. We describe patient characteristics, presentation, evaluation, and surgical approach of five patients with first BCAs. Results. Age at definitive surgical treatment ranged from 8 months to 7 years. Various clinical presentations were encountered, some of which were atypical for first BCAs. All had preoperative imaging demonstrating the tract. Four surgical approaches required a superficial parotidectomy with identification of the facial nerve, one of which revealed an aberrant facial nerve. In one case the tract was found to travel into the angle of the mandible, terminating as a mandibular cyst. This required en bloc excision that included the lateral cortex of the mandible. Conclusions. First BCAs have variable presentations. Complete surgical excision can be challenging. Therefore, careful preoperative planning and the recognition of atypical variants during surgery are essential. Hindawi Publishing Corporation 2016 2016-02-29 /pmc/articles/PMC4789415/ /pubmed/27034873 http://dx.doi.org/10.1155/2016/3902974 Text en Copyright © 2016 Lourdes Quintanilla-Dieck et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Quintanilla-Dieck, Lourdes Virgin, Frank Wootten, Chistopher Goudy, Steven Penn, Edward Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series |
title | Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series |
title_full | Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series |
title_fullStr | Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series |
title_full_unstemmed | Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series |
title_short | Surgical Approaches to First Branchial Cleft Anomaly Excision: A Case Series |
title_sort | surgical approaches to first branchial cleft anomaly excision: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789415/ https://www.ncbi.nlm.nih.gov/pubmed/27034873 http://dx.doi.org/10.1155/2016/3902974 |
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