Laryngeal epidermal inclusion cyst: report of an unusual case and literature review

The causes of dysphonia or hoarseness are numerous and can be classified as functional or organic. The report will highlight the clinical presentation, histopathological features and management plan of laryngeal epidermal inclusion cysts (EICs). Laryngeal EICs are rare. The epidermal and dermoid cys...

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Autores principales: Khushaim, Hanan, Albaghli, Slava, Al-Alsheikh, Abdulmalik, Al Rikabi, Ammar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703371/
https://www.ncbi.nlm.nih.gov/pubmed/33294169
http://dx.doi.org/10.1093/jscr/rjaa488
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author Khushaim, Hanan
Albaghli, Slava
Al-Alsheikh, Abdulmalik
Al Rikabi, Ammar
author_facet Khushaim, Hanan
Albaghli, Slava
Al-Alsheikh, Abdulmalik
Al Rikabi, Ammar
author_sort Khushaim, Hanan
collection PubMed
description The causes of dysphonia or hoarseness are numerous and can be classified as functional or organic. The report will highlight the clinical presentation, histopathological features and management plan of laryngeal epidermal inclusion cysts (EICs). Laryngeal EICs are rare. The epidermal and dermoid cysts represent only 0.01% of oral cavity cysts. Their clinical presentation varies from a completely asymptomatic presentation to dysphonia for years. This current report represents a case of a 34-year-old female who presented with 2-year history of dysphonia, which was caused by a unilateral laryngeal EIC.
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spelling pubmed-77033712020-12-07 Laryngeal epidermal inclusion cyst: report of an unusual case and literature review Khushaim, Hanan Albaghli, Slava Al-Alsheikh, Abdulmalik Al Rikabi, Ammar J Surg Case Rep Case Report The causes of dysphonia or hoarseness are numerous and can be classified as functional or organic. The report will highlight the clinical presentation, histopathological features and management plan of laryngeal epidermal inclusion cysts (EICs). Laryngeal EICs are rare. The epidermal and dermoid cysts represent only 0.01% of oral cavity cysts. Their clinical presentation varies from a completely asymptomatic presentation to dysphonia for years. This current report represents a case of a 34-year-old female who presented with 2-year history of dysphonia, which was caused by a unilateral laryngeal EIC. Oxford University Press 2020-11-30 /pmc/articles/PMC7703371/ /pubmed/33294169 http://dx.doi.org/10.1093/jscr/rjaa488 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2020. http://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/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Case Report
Khushaim, Hanan
Albaghli, Slava
Al-Alsheikh, Abdulmalik
Al Rikabi, Ammar
Laryngeal epidermal inclusion cyst: report of an unusual case and literature review
title Laryngeal epidermal inclusion cyst: report of an unusual case and literature review
title_full Laryngeal epidermal inclusion cyst: report of an unusual case and literature review
title_fullStr Laryngeal epidermal inclusion cyst: report of an unusual case and literature review
title_full_unstemmed Laryngeal epidermal inclusion cyst: report of an unusual case and literature review
title_short Laryngeal epidermal inclusion cyst: report of an unusual case and literature review
title_sort laryngeal epidermal inclusion cyst: report of an unusual case and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703371/
https://www.ncbi.nlm.nih.gov/pubmed/33294169
http://dx.doi.org/10.1093/jscr/rjaa488
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AT alalsheikhabdulmalik laryngealepidermalinclusioncystreportofanunusualcaseandliteraturereview
AT alrikabiammar laryngealepidermalinclusioncystreportofanunusualcaseandliteraturereview

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