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Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management

A case of a mandibular acanthomatous ameloblastoma, with an admixed little component of follicular type, is reported. The epidemiological features of the present case agree with those reported in the international literature. Clinico-radiographic differential diagnostic difficulties existed with sev...

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Autores principales: Pippi, Roberto, Santoro, Marcello, Pietrantoni, Alessandra, Pernazza, Angelina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235966/
https://www.ncbi.nlm.nih.gov/pubmed/34239735
http://dx.doi.org/10.1155/2021/9941779
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author Pippi, Roberto
Santoro, Marcello
Pietrantoni, Alessandra
Pernazza, Angelina
author_facet Pippi, Roberto
Santoro, Marcello
Pietrantoni, Alessandra
Pernazza, Angelina
author_sort Pippi, Roberto
collection PubMed
description A case of a mandibular acanthomatous ameloblastoma, with an admixed little component of follicular type, is reported. The epidemiological features of the present case agree with those reported in the international literature. Clinico-radiographic differential diagnostic difficulties existed with several other noncystic osteolytic lesions of the mandible. Recurrence was diagnosed early 1 year after the initial excisional biopsy, and a definitive rim resection was therefore performed. No further recurrence occurred in the following 4-year follow-up.
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spelling pubmed-82359662021-07-07 Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management Pippi, Roberto Santoro, Marcello Pietrantoni, Alessandra Pernazza, Angelina Case Rep Dent Case Report A case of a mandibular acanthomatous ameloblastoma, with an admixed little component of follicular type, is reported. The epidemiological features of the present case agree with those reported in the international literature. Clinico-radiographic differential diagnostic difficulties existed with several other noncystic osteolytic lesions of the mandible. Recurrence was diagnosed early 1 year after the initial excisional biopsy, and a definitive rim resection was therefore performed. No further recurrence occurred in the following 4-year follow-up. Hindawi 2021-06-18 /pmc/articles/PMC8235966/ /pubmed/34239735 http://dx.doi.org/10.1155/2021/9941779 Text en Copyright © 2021 Roberto Pippi et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Pippi, Roberto
Santoro, Marcello
Pietrantoni, Alessandra
Pernazza, Angelina
Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management
title Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management
title_full Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management
title_fullStr Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management
title_full_unstemmed Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management
title_short Acanthomatous Ameloblastoma: An Early Stage Case Report with Difficult Management
title_sort acanthomatous ameloblastoma: an early stage case report with difficult management
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8235966/
https://www.ncbi.nlm.nih.gov/pubmed/34239735
http://dx.doi.org/10.1155/2021/9941779
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