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A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?

Hemangiomas of the head and neck are considered to be benign tumors of infancy that are characterized by a rapid growth phase with endothelial cell proliferation, followed by gradual involution. Central hemangiomas are a rare occurrence and even rarer are the hybrid tumors of central hemangiomas wit...

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Autores principales: Jois, Harshvardhan S., Kumar K.P., Mohan, Kumar, Mandali Satish, Waghrey, Shefali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981335/
https://www.ncbi.nlm.nih.gov/pubmed/24765404
http://dx.doi.org/10.4081/cp.2012.e5
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author Jois, Harshvardhan S.
Kumar K.P., Mohan
Kumar, Mandali Satish
Waghrey, Shefali
author_facet Jois, Harshvardhan S.
Kumar K.P., Mohan
Kumar, Mandali Satish
Waghrey, Shefali
author_sort Jois, Harshvardhan S.
collection PubMed
description Hemangiomas of the head and neck are considered to be benign tumors of infancy that are characterized by a rapid growth phase with endothelial cell proliferation, followed by gradual involution. Central hemangiomas are a rare occurrence and even rarer are the hybrid tumors of central hemangiomas with odontogenic tumors such as ameloblastomas. This paper reports a case of one such hybrid tumor in a middle aged adult clinical presenting as a mandibular swelling with indistinct mixed radiographic presentation and histopathologically comprising of intimately associated hemangiomatous vascular channels and typical ameloblastic areas. To the authors' knowledge this is the sixth case of such a hemangiomatous ameloblastoma which has been reported till date.
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spelling pubmed-39813352014-04-24 A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant? Jois, Harshvardhan S. Kumar K.P., Mohan Kumar, Mandali Satish Waghrey, Shefali Clin Pract Case Report Hemangiomas of the head and neck are considered to be benign tumors of infancy that are characterized by a rapid growth phase with endothelial cell proliferation, followed by gradual involution. Central hemangiomas are a rare occurrence and even rarer are the hybrid tumors of central hemangiomas with odontogenic tumors such as ameloblastomas. This paper reports a case of one such hybrid tumor in a middle aged adult clinical presenting as a mandibular swelling with indistinct mixed radiographic presentation and histopathologically comprising of intimately associated hemangiomatous vascular channels and typical ameloblastic areas. To the authors' knowledge this is the sixth case of such a hemangiomatous ameloblastoma which has been reported till date. PAGEPress Publications 2011-12-30 /pmc/articles/PMC3981335/ /pubmed/24765404 http://dx.doi.org/10.4081/cp.2012.e5 Text en ©Copyright H.S. Jois et al., 2012 This work is licensed under a Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0). Licensee PAGEPress, Italy
spellingShingle Case Report
Jois, Harshvardhan S.
Kumar K.P., Mohan
Kumar, Mandali Satish
Waghrey, Shefali
A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
title A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
title_full A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
title_fullStr A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
title_full_unstemmed A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
title_short A mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
title_sort mixed neoplasm of intraosseous hemangioma with an ameloblastoma: a case of collision tumor or a rare variant?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981335/
https://www.ncbi.nlm.nih.gov/pubmed/24765404
http://dx.doi.org/10.4081/cp.2012.e5
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