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A rare case of huge maxillary ameloblastoma in a 3.5 years old girl

Ameloblastoma is a benign locally invasive odontogenic tumor. It is the most common odontogenic tumor [1]. Usually, in the middle-aged population, it is more common in the mandible with about 5–20% occurring in the maxilla. We report a case of maxillary unicystic ameloblastoma in a 3.5-year-old girl...

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Autores principales: El Sayed, Mohamed, Touny, Mohamed, Ibrahim, Nesreen, Al-Azzawi, Zainab
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306543/
https://www.ncbi.nlm.nih.gov/pubmed/32698263
http://dx.doi.org/10.1016/j.ijscr.2020.06.027
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author El Sayed, Mohamed
Touny, Mohamed
Ibrahim, Nesreen
Al-Azzawi, Zainab
author_facet El Sayed, Mohamed
Touny, Mohamed
Ibrahim, Nesreen
Al-Azzawi, Zainab
author_sort El Sayed, Mohamed
collection PubMed
description Ameloblastoma is a benign locally invasive odontogenic tumor. It is the most common odontogenic tumor [1]. Usually, in the middle-aged population, it is more common in the mandible with about 5–20% occurring in the maxilla. We report a case of maxillary unicystic ameloblastoma in a 3.5-year-old girl. Which presented clinically as a large facial swelling causing severe facial deformation and pressure symptoms on the left eye. CT scan showed that the swelling extended to involve the orbital floor. The lesion was diagnosed and confirmed by incisional biopsy then was successfully managed by maxillectomy and immediate reconstruction using the buccal pad of fat. One year follow up with no further complaints and no recurrence was observed. "Written informed consent was obtained from the patient guardians for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request”.
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spelling pubmed-73065432020-06-25 A rare case of huge maxillary ameloblastoma in a 3.5 years old girl El Sayed, Mohamed Touny, Mohamed Ibrahim, Nesreen Al-Azzawi, Zainab Int J Surg Case Rep Article Ameloblastoma is a benign locally invasive odontogenic tumor. It is the most common odontogenic tumor [1]. Usually, in the middle-aged population, it is more common in the mandible with about 5–20% occurring in the maxilla. We report a case of maxillary unicystic ameloblastoma in a 3.5-year-old girl. Which presented clinically as a large facial swelling causing severe facial deformation and pressure symptoms on the left eye. CT scan showed that the swelling extended to involve the orbital floor. The lesion was diagnosed and confirmed by incisional biopsy then was successfully managed by maxillectomy and immediate reconstruction using the buccal pad of fat. One year follow up with no further complaints and no recurrence was observed. "Written informed consent was obtained from the patient guardians for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal on request”. Elsevier 2020-06-12 /pmc/articles/PMC7306543/ /pubmed/32698263 http://dx.doi.org/10.1016/j.ijscr.2020.06.027 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
El Sayed, Mohamed
Touny, Mohamed
Ibrahim, Nesreen
Al-Azzawi, Zainab
A rare case of huge maxillary ameloblastoma in a 3.5 years old girl
title A rare case of huge maxillary ameloblastoma in a 3.5 years old girl
title_full A rare case of huge maxillary ameloblastoma in a 3.5 years old girl
title_fullStr A rare case of huge maxillary ameloblastoma in a 3.5 years old girl
title_full_unstemmed A rare case of huge maxillary ameloblastoma in a 3.5 years old girl
title_short A rare case of huge maxillary ameloblastoma in a 3.5 years old girl
title_sort rare case of huge maxillary ameloblastoma in a 3.5 years old girl
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306543/
https://www.ncbi.nlm.nih.gov/pubmed/32698263
http://dx.doi.org/10.1016/j.ijscr.2020.06.027
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