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Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case

Ameloblastomas demonstrate various clinical and microscopic patterns. They typically have been described as possessing three biologic variants including solid, cystic (unicystic) and peripheral, of which about 13% to 21% of all cases are unicystic. Granular cell subtype is a rare variant especially...

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Autores principales: Sargolzaei, Soudabeh, Atarbashi-Moghadam, Saede, Roohi, Aliasghar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890815/
https://www.ncbi.nlm.nih.gov/pubmed/31875179
http://dx.doi.org/10.30476/DENTJODS.2019.44907
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author Sargolzaei, Soudabeh
Atarbashi-Moghadam, Saede
Roohi, Aliasghar
author_facet Sargolzaei, Soudabeh
Atarbashi-Moghadam, Saede
Roohi, Aliasghar
author_sort Sargolzaei, Soudabeh
collection PubMed
description Ameloblastomas demonstrate various clinical and microscopic patterns. They typically have been described as possessing three biologic variants including solid, cystic (unicystic) and peripheral, of which about 13% to 21% of all cases are unicystic. Granular cell subtype is a rare variant especially when both the inner and peripheral layers of tumoral islands composed exclusively of eosinophilic granular cells. The purpose of this case report is to present a unique case of cystic ameloblastoma with an unusual radiographic and microscopic pattern affecting a 25-year-old female. Awareness of these rare histopathologic features for oral pathologist is essential to help correct diagnosis.
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spelling pubmed-68908152019-12-24 Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case Sargolzaei, Soudabeh Atarbashi-Moghadam, Saede Roohi, Aliasghar J Dent (Shiraz) Case Reports Ameloblastomas demonstrate various clinical and microscopic patterns. They typically have been described as possessing three biologic variants including solid, cystic (unicystic) and peripheral, of which about 13% to 21% of all cases are unicystic. Granular cell subtype is a rare variant especially when both the inner and peripheral layers of tumoral islands composed exclusively of eosinophilic granular cells. The purpose of this case report is to present a unique case of cystic ameloblastoma with an unusual radiographic and microscopic pattern affecting a 25-year-old female. Awareness of these rare histopathologic features for oral pathologist is essential to help correct diagnosis. Shiraz University of Medical Sciences 2019-12 /pmc/articles/PMC6890815/ /pubmed/31875179 http://dx.doi.org/10.30476/DENTJODS.2019.44907 Text en Copyright: © Shiraz University of Medical Sciences 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 Reports
Sargolzaei, Soudabeh
Atarbashi-Moghadam, Saede
Roohi, Aliasghar
Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case
title Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case
title_full Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case
title_fullStr Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case
title_full_unstemmed Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case
title_short Mandibular Mural Ameloblastoma with Unusual Histopathologic Features: a Rare Challenging Case
title_sort mandibular mural ameloblastoma with unusual histopathologic features: a rare challenging case
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890815/
https://www.ncbi.nlm.nih.gov/pubmed/31875179
http://dx.doi.org/10.30476/DENTJODS.2019.44907
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AT roohialiasghar mandibularmuralameloblastomawithunusualhistopathologicfeaturesararechallengingcase