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Hemangiomatous ameloblastoma in maxilla: A report of a very rare case
Hemangiomatous ameloblastoma (HA), which is a rare ameloblastic variant, is presented in a 15-year-old boy in the maxillary right molar region associated with unerupted canine and premolars. Radiologic and computed tomographic analysis was suggestive of cystic lesion. An histology picture confirmed...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469904/ https://www.ncbi.nlm.nih.gov/pubmed/23087743 |
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author | Sharma, Vivek K. Verma, Sanjeev K. Goyal, Lata Chaudhary, Prabhat Kumar |
author_facet | Sharma, Vivek K. Verma, Sanjeev K. Goyal, Lata Chaudhary, Prabhat Kumar |
author_sort | Sharma, Vivek K. |
collection | PubMed |
description | Hemangiomatous ameloblastoma (HA), which is a rare ameloblastic variant, is presented in a 15-year-old boy in the maxillary right molar region associated with unerupted canine and premolars. Radiologic and computed tomographic analysis was suggestive of cystic lesion. An histology picture confirmed the diagnosis of HA. There are less than eight cases documented in the literature and mostly are in the middle age with mandibular location. This is first ever reported case of HA in a 15-year-old boy with maxillary location. Due to less number of documented cases and no long-term follow-ups, clinical behavior and prognosis of this lesion are uncertain. In this case report, the clinical, histological, and radiographic features of HA are presented. |
format | Online Article Text |
id | pubmed-3469904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34699042012-10-19 Hemangiomatous ameloblastoma in maxilla: A report of a very rare case Sharma, Vivek K. Verma, Sanjeev K. Goyal, Lata Chaudhary, Prabhat Kumar Dent Res J (Isfahan) Case Report Hemangiomatous ameloblastoma (HA), which is a rare ameloblastic variant, is presented in a 15-year-old boy in the maxillary right molar region associated with unerupted canine and premolars. Radiologic and computed tomographic analysis was suggestive of cystic lesion. An histology picture confirmed the diagnosis of HA. There are less than eight cases documented in the literature and mostly are in the middle age with mandibular location. This is first ever reported case of HA in a 15-year-old boy with maxillary location. Due to less number of documented cases and no long-term follow-ups, clinical behavior and prognosis of this lesion are uncertain. In this case report, the clinical, histological, and radiographic features of HA are presented. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3469904/ /pubmed/23087743 Text en Copyright: © Dental Research Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Sharma, Vivek K. Verma, Sanjeev K. Goyal, Lata Chaudhary, Prabhat Kumar Hemangiomatous ameloblastoma in maxilla: A report of a very rare case |
title | Hemangiomatous ameloblastoma in maxilla: A report of a very rare case |
title_full | Hemangiomatous ameloblastoma in maxilla: A report of a very rare case |
title_fullStr | Hemangiomatous ameloblastoma in maxilla: A report of a very rare case |
title_full_unstemmed | Hemangiomatous ameloblastoma in maxilla: A report of a very rare case |
title_short | Hemangiomatous ameloblastoma in maxilla: A report of a very rare case |
title_sort | hemangiomatous ameloblastoma in maxilla: a report of a very rare case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469904/ https://www.ncbi.nlm.nih.gov/pubmed/23087743 |
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