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Soft-tissue osteoma of the temple

A 65-year-old woman presented with a solid mass on the right temporal area. The mass had grown for over 2 years without any initiating event of trauma or inflammation. Before excision, the patient went through a computed tomography scan, revealing a calcified mass without bony connection. Under gene...

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Detalles Bibliográficos
Autores principales: Roh, Si-Gyun, Kim, Yun-Seob, Kim, Jong-Lim, Shin, Jin-Yong, Lee, Nae-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cleft Palate-Craniofacial Association 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568491/
https://www.ncbi.nlm.nih.gov/pubmed/34732040
http://dx.doi.org/10.7181/acfs.2021.00388
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author Roh, Si-Gyun
Kim, Yun-Seob
Kim, Jong-Lim
Shin, Jin-Yong
Lee, Nae-Ho
author_facet Roh, Si-Gyun
Kim, Yun-Seob
Kim, Jong-Lim
Shin, Jin-Yong
Lee, Nae-Ho
author_sort Roh, Si-Gyun
collection PubMed
description A 65-year-old woman presented with a solid mass on the right temporal area. The mass had grown for over 2 years without any initiating event of trauma or inflammation. Before excision, the patient went through a computed tomography scan, revealing a calcified mass without bony connection. Under general anesthesia, an excisional biopsy was performed. Microscopic examination confirmed a diagnosis of soft tissue osteoma. Soft tissue osteoma is rare, especially in the head and neck region. Osteomas in the temporal region have not been reported yet. Due to its rarity, osteoma might be misdiagnosed as another soft tissue or bone origin tumor. Its treatment of choice is simple excision. In this review, we present an unusual clinical form of soft tissue osteoma.
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spelling pubmed-85684912021-11-18 Soft-tissue osteoma of the temple Roh, Si-Gyun Kim, Yun-Seob Kim, Jong-Lim Shin, Jin-Yong Lee, Nae-Ho Arch Craniofac Surg Case Report A 65-year-old woman presented with a solid mass on the right temporal area. The mass had grown for over 2 years without any initiating event of trauma or inflammation. Before excision, the patient went through a computed tomography scan, revealing a calcified mass without bony connection. Under general anesthesia, an excisional biopsy was performed. Microscopic examination confirmed a diagnosis of soft tissue osteoma. Soft tissue osteoma is rare, especially in the head and neck region. Osteomas in the temporal region have not been reported yet. Due to its rarity, osteoma might be misdiagnosed as another soft tissue or bone origin tumor. Its treatment of choice is simple excision. In this review, we present an unusual clinical form of soft tissue osteoma. Korean Cleft Palate-Craniofacial Association 2021-10 2021-10-20 /pmc/articles/PMC8568491/ /pubmed/34732040 http://dx.doi.org/10.7181/acfs.2021.00388 Text en Copyright © 2021 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
Roh, Si-Gyun
Kim, Yun-Seob
Kim, Jong-Lim
Shin, Jin-Yong
Lee, Nae-Ho
Soft-tissue osteoma of the temple
title Soft-tissue osteoma of the temple
title_full Soft-tissue osteoma of the temple
title_fullStr Soft-tissue osteoma of the temple
title_full_unstemmed Soft-tissue osteoma of the temple
title_short Soft-tissue osteoma of the temple
title_sort soft-tissue osteoma of the temple
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8568491/
https://www.ncbi.nlm.nih.gov/pubmed/34732040
http://dx.doi.org/10.7181/acfs.2021.00388
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