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Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up

Ameloblastic fibrosarcoma (AFS) is a rare malignant mixed odontogenic tumor which is usually considered as the malignant counterpart of ameloblastic fibroma. Only mesenchymal component represents sarcomatous alterations and ameloblast-like epithelial nest remains bland in AFS. Here, we report a case...

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Detalles Bibliográficos
Autores principales: Khalili, Maryam, Shakib, Pouyan Amini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714812/
https://www.ncbi.nlm.nih.gov/pubmed/23878574
http://dx.doi.org/10.4103/1735-3327.111812
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author Khalili, Maryam
Shakib, Pouyan Amini
author_facet Khalili, Maryam
Shakib, Pouyan Amini
author_sort Khalili, Maryam
collection PubMed
description Ameloblastic fibrosarcoma (AFS) is a rare malignant mixed odontogenic tumor which is usually considered as the malignant counterpart of ameloblastic fibroma. Only mesenchymal component represents sarcomatous alterations and ameloblast-like epithelial nest remains bland in AFS. Here, we report a case of AFS in a 26-year-old man in the maxilla, which was regarded as an uncommon location for this tumor. After 2 years follow up, no evidence of recurrence was noted. We also emphasize on comprehensive clinical, radiographic, and histopathologic evaluation of such patients rather than immunohistochemical staining to make an accurate diagnosis.
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spelling pubmed-37148122013-07-22 Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up Khalili, Maryam Shakib, Pouyan Amini Dent Res J (Isfahan) Case Report Ameloblastic fibrosarcoma (AFS) is a rare malignant mixed odontogenic tumor which is usually considered as the malignant counterpart of ameloblastic fibroma. Only mesenchymal component represents sarcomatous alterations and ameloblast-like epithelial nest remains bland in AFS. Here, we report a case of AFS in a 26-year-old man in the maxilla, which was regarded as an uncommon location for this tumor. After 2 years follow up, no evidence of recurrence was noted. We also emphasize on comprehensive clinical, radiographic, and histopathologic evaluation of such patients rather than immunohistochemical staining to make an accurate diagnosis. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3714812/ /pubmed/23878574 http://dx.doi.org/10.4103/1735-3327.111812 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
Khalili, Maryam
Shakib, Pouyan Amini
Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up
title Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up
title_full Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up
title_fullStr Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up
title_full_unstemmed Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up
title_short Ameloblastic fibrosarcoma of the upper jaw: Report of a rare case with long-term follow-up
title_sort ameloblastic fibrosarcoma of the upper jaw: report of a rare case with long-term follow-up
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3714812/
https://www.ncbi.nlm.nih.gov/pubmed/23878574
http://dx.doi.org/10.4103/1735-3327.111812
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