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Retromastoid osteoma—a rare case report

Osteomas are slow growing bone tumours and are often asymptomatic. Rarely, they can be present in the temporal bone—only few cases had been reported, with an incidence of 0.1–1%. We describe a case of an osteoma of the temporal bone (retromastoid) found in a 40 year old female, who presented with a...

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Detalles Bibliográficos
Autores principales: Tan, Edmund Wooi Keat, Barco, Jason Bae, Rehman, Mutee Ur, Tan, Choon Chieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963170/
https://www.ncbi.nlm.nih.gov/pubmed/31976061
http://dx.doi.org/10.1093/jscr/rjz381
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author Tan, Edmund Wooi Keat
Barco, Jason Bae
Rehman, Mutee Ur
Tan, Choon Chieh
author_facet Tan, Edmund Wooi Keat
Barco, Jason Bae
Rehman, Mutee Ur
Tan, Choon Chieh
author_sort Tan, Edmund Wooi Keat
collection PubMed
description Osteomas are slow growing bone tumours and are often asymptomatic. Rarely, they can be present in the temporal bone—only few cases had been reported, with an incidence of 0.1–1%. We describe a case of an osteoma of the temporal bone (retromastoid) found in a 40 year old female, who presented with a slow growing swelling behind the right ear for 9 years. Diagnosis was made on non-contrast computed topography (CT) of the skull. Treatment is indicated in symptomatic cases or cosmetic reasons. Screening colonoscopy and genetic testing for familial adenomatous polyposis (FAP) and Gardner’s syndrome are advised.
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spelling pubmed-69631702020-01-23 Retromastoid osteoma—a rare case report Tan, Edmund Wooi Keat Barco, Jason Bae Rehman, Mutee Ur Tan, Choon Chieh J Surg Case Rep Case Report Osteomas are slow growing bone tumours and are often asymptomatic. Rarely, they can be present in the temporal bone—only few cases had been reported, with an incidence of 0.1–1%. We describe a case of an osteoma of the temporal bone (retromastoid) found in a 40 year old female, who presented with a slow growing swelling behind the right ear for 9 years. Diagnosis was made on non-contrast computed topography (CT) of the skull. Treatment is indicated in symptomatic cases or cosmetic reasons. Screening colonoscopy and genetic testing for familial adenomatous polyposis (FAP) and Gardner’s syndrome are advised. Oxford University Press 2020-01-13 /pmc/articles/PMC6963170/ /pubmed/31976061 http://dx.doi.org/10.1093/jscr/rjz381 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
Tan, Edmund Wooi Keat
Barco, Jason Bae
Rehman, Mutee Ur
Tan, Choon Chieh
Retromastoid osteoma—a rare case report
title Retromastoid osteoma—a rare case report
title_full Retromastoid osteoma—a rare case report
title_fullStr Retromastoid osteoma—a rare case report
title_full_unstemmed Retromastoid osteoma—a rare case report
title_short Retromastoid osteoma—a rare case report
title_sort retromastoid osteoma—a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963170/
https://www.ncbi.nlm.nih.gov/pubmed/31976061
http://dx.doi.org/10.1093/jscr/rjz381
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