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Unicystic ameloblastoma of the mandible - an unusual case report and review of literature

Ameloblastoma is a true neoplasm of odontogenic epithelial origin. It is the second most common odontogenic neoplasm, and only odontoma outnumbers it in reported frequency of occurrence. Its incidence, combined with its clinical behavior, makes ameloblastoma the most significant odontogenic neoplasm...

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Autores principales: Ramesh, Rakesh S, Manjunath, Suraj, Ustad, Tanveer H, Pais, Saira, Shivakumar, K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821325/
https://www.ncbi.nlm.nih.gov/pubmed/20157425
http://dx.doi.org/10.1186/1758-3284-2-1
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author Ramesh, Rakesh S
Manjunath, Suraj
Ustad, Tanveer H
Pais, Saira
Shivakumar, K
author_facet Ramesh, Rakesh S
Manjunath, Suraj
Ustad, Tanveer H
Pais, Saira
Shivakumar, K
author_sort Ramesh, Rakesh S
collection PubMed
description Ameloblastoma is a true neoplasm of odontogenic epithelial origin. It is the second most common odontogenic neoplasm, and only odontoma outnumbers it in reported frequency of occurrence. Its incidence, combined with its clinical behavior, makes ameloblastoma the most significant odontogenic neoplasm. Unicystic ameloblastoma (UA) refers to those cystic lesions that show clinical, radiographic, or gross features of a mandibular cyst, but on histologic examination show a typical ameloblastomatous epithelium lining part of the cyst cavity, with or without luminal and/or mural tumor growth. It accounts for 5-15% of all intraosseous ameloblastomas. We report a case of unicystic ameloblastoma in a 30-year-old female, and review the literature.
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spelling pubmed-28213252010-02-15 Unicystic ameloblastoma of the mandible - an unusual case report and review of literature Ramesh, Rakesh S Manjunath, Suraj Ustad, Tanveer H Pais, Saira Shivakumar, K Head Neck Oncol Review Ameloblastoma is a true neoplasm of odontogenic epithelial origin. It is the second most common odontogenic neoplasm, and only odontoma outnumbers it in reported frequency of occurrence. Its incidence, combined with its clinical behavior, makes ameloblastoma the most significant odontogenic neoplasm. Unicystic ameloblastoma (UA) refers to those cystic lesions that show clinical, radiographic, or gross features of a mandibular cyst, but on histologic examination show a typical ameloblastomatous epithelium lining part of the cyst cavity, with or without luminal and/or mural tumor growth. It accounts for 5-15% of all intraosseous ameloblastomas. We report a case of unicystic ameloblastoma in a 30-year-old female, and review the literature. BioMed Central 2010-01-14 /pmc/articles/PMC2821325/ /pubmed/20157425 http://dx.doi.org/10.1186/1758-3284-2-1 Text en Copyright ©2010 Ramesh et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Ramesh, Rakesh S
Manjunath, Suraj
Ustad, Tanveer H
Pais, Saira
Shivakumar, K
Unicystic ameloblastoma of the mandible - an unusual case report and review of literature
title Unicystic ameloblastoma of the mandible - an unusual case report and review of literature
title_full Unicystic ameloblastoma of the mandible - an unusual case report and review of literature
title_fullStr Unicystic ameloblastoma of the mandible - an unusual case report and review of literature
title_full_unstemmed Unicystic ameloblastoma of the mandible - an unusual case report and review of literature
title_short Unicystic ameloblastoma of the mandible - an unusual case report and review of literature
title_sort unicystic ameloblastoma of the mandible - an unusual case report and review of literature
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821325/
https://www.ncbi.nlm.nih.gov/pubmed/20157425
http://dx.doi.org/10.1186/1758-3284-2-1
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