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Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature

Oral melanoacanthoma is rare pigmented mucosal lesion that presents most commonly on the buccal mucosa, characterized by sudden appearance and rapid radial growth, thus clinically mimicking malignant melanoma. It was originally described as a mixed tumor of melanocytes and keratinocytes, but appears...

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Autores principales: Rohilla, Kshitiz, Ramesh, V, Balamurali, PD, Singh, Namrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034627/
https://www.ncbi.nlm.nih.gov/pubmed/25206187
http://dx.doi.org/10.5005/jp-journals-10005-1185
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author Rohilla, Kshitiz
Ramesh, V
Balamurali, PD
Singh, Namrata
author_facet Rohilla, Kshitiz
Ramesh, V
Balamurali, PD
Singh, Namrata
author_sort Rohilla, Kshitiz
collection PubMed
description Oral melanoacanthoma is rare pigmented mucosal lesion that presents most commonly on the buccal mucosa, characterized by sudden appearance and rapid radial growth, thus clinically mimicking malignant melanoma. It was originally described as a mixed tumor of melanocytes and keratinocytes, but appears to be a reactive process; formed in areas prone to trauma, and regressing after the removal of trauma or incomplete excision. The clinical appearance of oral melanoacanthoma is nondiagnostic, and biopsy is mandatory to rule out malignancy. We report a case of melanoacanthoma of a rarer oral mucosal site in a 12-year-old Asian male. A brief review of the current literature is also presented. How to cite this article: Rohilla K, Ramesh V, Balamurali PD, Singh N. Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature. Int J Clin Pediatr Dent 2013;6(1):40-43.
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spelling pubmed-40346272014-09-09 Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature Rohilla, Kshitiz Ramesh, V Balamurali, PD Singh, Namrata Int J Clin Pediatr Dent Case Report Oral melanoacanthoma is rare pigmented mucosal lesion that presents most commonly on the buccal mucosa, characterized by sudden appearance and rapid radial growth, thus clinically mimicking malignant melanoma. It was originally described as a mixed tumor of melanocytes and keratinocytes, but appears to be a reactive process; formed in areas prone to trauma, and regressing after the removal of trauma or incomplete excision. The clinical appearance of oral melanoacanthoma is nondiagnostic, and biopsy is mandatory to rule out malignancy. We report a case of melanoacanthoma of a rarer oral mucosal site in a 12-year-old Asian male. A brief review of the current literature is also presented. How to cite this article: Rohilla K, Ramesh V, Balamurali PD, Singh N. Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature. Int J Clin Pediatr Dent 2013;6(1):40-43. Jaypee Brothers Medical Publishers 2013 2013-04-26 /pmc/articles/PMC4034627/ /pubmed/25206187 http://dx.doi.org/10.5005/jp-journals-10005-1185 Text en Copyright © 2013; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Rohilla, Kshitiz
Ramesh, V
Balamurali, PD
Singh, Namrata
Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature
title Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature
title_full Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature
title_fullStr Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature
title_full_unstemmed Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature
title_short Oral Melanoacanthoma of a Rare Intraoral Site: Case Report and Review of Literature
title_sort oral melanoacanthoma of a rare intraoral site: case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4034627/
https://www.ncbi.nlm.nih.gov/pubmed/25206187
http://dx.doi.org/10.5005/jp-journals-10005-1185
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