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Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review
Calcifying cystic odontogenic tumor (CCOT) is a rare lesion accounting for only 2% of all odontogenic cysts and tumors. CCOTs can occur alone or in association with other odontogenic tumors such as odontomas. Pigmented intraosseous odontogenic lesions are rare. Among them, pigmented CCOT is known to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421910/ https://www.ncbi.nlm.nih.gov/pubmed/30967731 http://dx.doi.org/10.4103/jomfp.JOMFP_253_17 |
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author | Premalatha, B R Sreeshyla, H S Nitin, Priyanka Hegde, Usha |
author_facet | Premalatha, B R Sreeshyla, H S Nitin, Priyanka Hegde, Usha |
author_sort | Premalatha, B R |
collection | PubMed |
description | Calcifying cystic odontogenic tumor (CCOT) is a rare lesion accounting for only 2% of all odontogenic cysts and tumors. CCOTs can occur alone or in association with other odontogenic tumors such as odontomas. Pigmented intraosseous odontogenic lesions are rare. Among them, pigmented CCOT is known to occur with greater frequency. Only six cases of combination of pigmentation CCOT associated with odontoma have been reported in the literature. We herein present such a rare case occurring in the maxillary anterior region in a 13-year-old female patient. |
format | Online Article Text |
id | pubmed-6421910 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-64219102019-04-09 Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review Premalatha, B R Sreeshyla, H S Nitin, Priyanka Hegde, Usha J Oral Maxillofac Pathol Case Report Calcifying cystic odontogenic tumor (CCOT) is a rare lesion accounting for only 2% of all odontogenic cysts and tumors. CCOTs can occur alone or in association with other odontogenic tumors such as odontomas. Pigmented intraosseous odontogenic lesions are rare. Among them, pigmented CCOT is known to occur with greater frequency. Only six cases of combination of pigmentation CCOT associated with odontoma have been reported in the literature. We herein present such a rare case occurring in the maxillary anterior region in a 13-year-old female patient. Medknow Publications & Media Pvt Ltd 2019-02 /pmc/articles/PMC6421910/ /pubmed/30967731 http://dx.doi.org/10.4103/jomfp.JOMFP_253_17 Text en Copyright: © 2019 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 Premalatha, B R Sreeshyla, H S Nitin, Priyanka Hegde, Usha Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review |
title | Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review |
title_full | Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review |
title_fullStr | Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review |
title_full_unstemmed | Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review |
title_short | Pigmented calcifying cystic odontogenic tumor associated with compound odontoma: Report of a rare case and review |
title_sort | pigmented calcifying cystic odontogenic tumor associated with compound odontoma: report of a rare case and review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421910/ https://www.ncbi.nlm.nih.gov/pubmed/30967731 http://dx.doi.org/10.4103/jomfp.JOMFP_253_17 |
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