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Plexiform Ameloblastoma

The ameloblastoma is a benign but aggressive neoplasm of odontogenic origin. However, no enamel or hard tissue is formed by the tumor cells. Ameloblastomas are infamous for their invasive growth and their tendency to recur. Robinson (1937) as a benign tumor that is ‘usually unicentric, nonfunctional...

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Autores principales: Celur, Sreelalita, Babu, K Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4093637/
https://www.ncbi.nlm.nih.gov/pubmed/25206141
http://dx.doi.org/10.5005/jp-journals-10005-1140
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author Celur, Sreelalita
Babu, K Sunil
author_facet Celur, Sreelalita
Babu, K Sunil
author_sort Celur, Sreelalita
collection PubMed
description The ameloblastoma is a benign but aggressive neoplasm of odontogenic origin. However, no enamel or hard tissue is formed by the tumor cells. Ameloblastomas are infamous for their invasive growth and their tendency to recur. Robinson (1937) as a benign tumor that is ‘usually unicentric, nonfunctional, intermittent in growth, anatomically benign and clinically persistent.’ They may occur at any age, even though nearly half of the tumors do occur between the ages of 20 and 40 years. This is the most common neoplasm affecting the jaws, yet only accounts for 1% of all tumors of the maxilla and mandible and 11% of all odontogenic tumors. This report presents a case of ameloblastoma involving entire ramus and part of body of mandible with resorption of the mesial and distal root apices of second molar and distal root of mandibular first molar. The lesion extending till the base of mandible surrounding the crown of the unerupted third molar resembling the dentigerous cyst. This was surgically resected followed by harvesting the contralateral sixth costochondral rib graft. How to cite this article: Celur S, Babu KS. Plexiform Ameloblastoma. Int J Clin Pediatr Dent 2012;5(1):78-83.
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spelling pubmed-40936372014-09-09 Plexiform Ameloblastoma Celur, Sreelalita Babu, K Sunil Int J Clin Pediatr Dent Case Report The ameloblastoma is a benign but aggressive neoplasm of odontogenic origin. However, no enamel or hard tissue is formed by the tumor cells. Ameloblastomas are infamous for their invasive growth and their tendency to recur. Robinson (1937) as a benign tumor that is ‘usually unicentric, nonfunctional, intermittent in growth, anatomically benign and clinically persistent.’ They may occur at any age, even though nearly half of the tumors do occur between the ages of 20 and 40 years. This is the most common neoplasm affecting the jaws, yet only accounts for 1% of all tumors of the maxilla and mandible and 11% of all odontogenic tumors. This report presents a case of ameloblastoma involving entire ramus and part of body of mandible with resorption of the mesial and distal root apices of second molar and distal root of mandibular first molar. The lesion extending till the base of mandible surrounding the crown of the unerupted third molar resembling the dentigerous cyst. This was surgically resected followed by harvesting the contralateral sixth costochondral rib graft. How to cite this article: Celur S, Babu KS. Plexiform Ameloblastoma. Int J Clin Pediatr Dent 2012;5(1):78-83. Jaypee Brothers Medical Publishers 2012 2012-02-24 /pmc/articles/PMC4093637/ /pubmed/25206141 http://dx.doi.org/10.5005/jp-journals-10005-1140 Text en Copyright © 2012; Jaypee Brothers Medical Publishers (P) Ltd. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Case Report
Celur, Sreelalita
Babu, K Sunil
Plexiform Ameloblastoma
title Plexiform Ameloblastoma
title_full Plexiform Ameloblastoma
title_fullStr Plexiform Ameloblastoma
title_full_unstemmed Plexiform Ameloblastoma
title_short Plexiform Ameloblastoma
title_sort plexiform ameloblastoma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4093637/
https://www.ncbi.nlm.nih.gov/pubmed/25206141
http://dx.doi.org/10.5005/jp-journals-10005-1140
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