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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...

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Autores principales: Sharma, Vivek K., Verma, Sanjeev K., Goyal, Lata, Chaudhary, Prabhat Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
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.
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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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