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Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report

INTRODUCTION AND IMPORTANCE: Diagnosis of odontogenic tumors can be challenging due to their rarity and diverse morphology. The clinical diagnosis could be suspected when it had raised near the tooth. But, when their location is not typical, like inside the paranasal sinuses, the diagnosis is less e...

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Autores principales: Chebil, Azer, Hasnaoui, Mahdi, Bhar, Salma, Masmoudi, Mohamed, Bellalah, Ahlem, Mighri, Kalifa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400081/
https://www.ncbi.nlm.nih.gov/pubmed/35969907
http://dx.doi.org/10.1016/j.ijscr.2022.107457
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author Chebil, Azer
Hasnaoui, Mahdi
Bhar, Salma
Masmoudi, Mohamed
Bellalah, Ahlem
Mighri, Kalifa
author_facet Chebil, Azer
Hasnaoui, Mahdi
Bhar, Salma
Masmoudi, Mohamed
Bellalah, Ahlem
Mighri, Kalifa
author_sort Chebil, Azer
collection PubMed
description INTRODUCTION AND IMPORTANCE: Diagnosis of odontogenic tumors can be challenging due to their rarity and diverse morphology. The clinical diagnosis could be suspected when it had raised near the tooth. But, when their location is not typical, like inside the paranasal sinuses, the diagnosis is less easy. Maxillary ameloblastomas are rare with only sparse information on their epidemiological, histological and effective management. CASE PRESENTATION: A 54-year-old woman presented with ameloblastoma of the left maxillary sinus. Intraoral examination revealed partially edentulous with a 2 cm painless ulceration of the left alveolar process of the maxilla. A biopsy was performed which showed a follicular ameloblastoma. The treatment was surgical. She had a combined endoscopic and transoral resection of the tumor. The patient was diagnosed with recurrence within 3 months from surgery. DISCUSSION: although rarely reported, clinicians should still suspect and know how to manage such as rare and locally invasive tumor as a maxillary ameloblastoma. CONCLUSIONS: As odontogenic tumors are rare, some entities are infrequently encountered, making the diagnosis more difficult. Clinicians, oral and maxillofacial surgeons, and oral pathologists should be familiar with the ameloblastoma and its differential diagnosis for accurate diagnosis and management.
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spelling pubmed-94000812022-08-25 Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report Chebil, Azer Hasnaoui, Mahdi Bhar, Salma Masmoudi, Mohamed Bellalah, Ahlem Mighri, Kalifa Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Diagnosis of odontogenic tumors can be challenging due to their rarity and diverse morphology. The clinical diagnosis could be suspected when it had raised near the tooth. But, when their location is not typical, like inside the paranasal sinuses, the diagnosis is less easy. Maxillary ameloblastomas are rare with only sparse information on their epidemiological, histological and effective management. CASE PRESENTATION: A 54-year-old woman presented with ameloblastoma of the left maxillary sinus. Intraoral examination revealed partially edentulous with a 2 cm painless ulceration of the left alveolar process of the maxilla. A biopsy was performed which showed a follicular ameloblastoma. The treatment was surgical. She had a combined endoscopic and transoral resection of the tumor. The patient was diagnosed with recurrence within 3 months from surgery. DISCUSSION: although rarely reported, clinicians should still suspect and know how to manage such as rare and locally invasive tumor as a maxillary ameloblastoma. CONCLUSIONS: As odontogenic tumors are rare, some entities are infrequently encountered, making the diagnosis more difficult. Clinicians, oral and maxillofacial surgeons, and oral pathologists should be familiar with the ameloblastoma and its differential diagnosis for accurate diagnosis and management. Elsevier 2022-08-02 /pmc/articles/PMC9400081/ /pubmed/35969907 http://dx.doi.org/10.1016/j.ijscr.2022.107457 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Chebil, Azer
Hasnaoui, Mahdi
Bhar, Salma
Masmoudi, Mohamed
Bellalah, Ahlem
Mighri, Kalifa
Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report
title Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report
title_full Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report
title_fullStr Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report
title_full_unstemmed Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report
title_short Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report
title_sort asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9400081/
https://www.ncbi.nlm.nih.gov/pubmed/35969907
http://dx.doi.org/10.1016/j.ijscr.2022.107457
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