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Compact osteoma of the maxilla: A rare case report

Osteomas of the facial bones are a rare entity and very few cases have been reported in the literature. Osteoma is a benign osteogenic lesion with a very slow growth, characterized by proliferation of either cancellous or compact bone. This paper describes a case of a 27 year old male seeking treatm...

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Autores principales: Yadalam, Umesh, Roy, Partha Pratim, Bose, Aditi, Smitha, T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269316/
https://www.ncbi.nlm.nih.gov/pubmed/32508471
http://dx.doi.org/10.4103/jomfp.JOMFP_223_19
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author Yadalam, Umesh
Roy, Partha Pratim
Bose, Aditi
Smitha, T
author_facet Yadalam, Umesh
Roy, Partha Pratim
Bose, Aditi
Smitha, T
author_sort Yadalam, Umesh
collection PubMed
description Osteomas of the facial bones are a rare entity and very few cases have been reported in the literature. Osteoma is a benign osteogenic lesion with a very slow growth, characterized by proliferation of either cancellous or compact bone. This paper describes a case of a 27 year old male seeking treatment for a slowly enlarging lesion in the maxillary right anterior region. Surgical excision of the lesion was done and the histopathologic evaluation revealed dense compact bone with osteocytes in the lacunae suggestive of compact osteoma. One year followup showed no evidence of recurrence. To best of our knowledge this is the twelfth case of maxillary osteoma reported in English language literature.
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spelling pubmed-72693162020-06-05 Compact osteoma of the maxilla: A rare case report Yadalam, Umesh Roy, Partha Pratim Bose, Aditi Smitha, T J Oral Maxillofac Pathol Case Report Osteomas of the facial bones are a rare entity and very few cases have been reported in the literature. Osteoma is a benign osteogenic lesion with a very slow growth, characterized by proliferation of either cancellous or compact bone. This paper describes a case of a 27 year old male seeking treatment for a slowly enlarging lesion in the maxillary right anterior region. Surgical excision of the lesion was done and the histopathologic evaluation revealed dense compact bone with osteocytes in the lacunae suggestive of compact osteoma. One year followup showed no evidence of recurrence. To best of our knowledge this is the twelfth case of maxillary osteoma reported in English language literature. Wolters Kluwer - Medknow 2020 2020-05-08 /pmc/articles/PMC7269316/ /pubmed/32508471 http://dx.doi.org/10.4103/jomfp.JOMFP_223_19 Text en Copyright: © 2020 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Yadalam, Umesh
Roy, Partha Pratim
Bose, Aditi
Smitha, T
Compact osteoma of the maxilla: A rare case report
title Compact osteoma of the maxilla: A rare case report
title_full Compact osteoma of the maxilla: A rare case report
title_fullStr Compact osteoma of the maxilla: A rare case report
title_full_unstemmed Compact osteoma of the maxilla: A rare case report
title_short Compact osteoma of the maxilla: A rare case report
title_sort compact osteoma of the maxilla: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7269316/
https://www.ncbi.nlm.nih.gov/pubmed/32508471
http://dx.doi.org/10.4103/jomfp.JOMFP_223_19
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