Asymptomatic ameloblastoma of the maxilla with infratemporal fossa involvement: A case report.
Ameloblastoma
Maxillary
Sinonasal tumor
Journal
International journal of surgery case reports
ISSN: 2210-2612
Titre abrégé: Int J Surg Case Rep
Pays: Netherlands
ID NLM: 101529872
Informations de publication
Date de publication:
Sep 2022
Sep 2022
Historique:
received:
23
06
2022
revised:
22
07
2022
accepted:
24
07
2022
pubmed:
16
8
2022
medline:
16
8
2022
entrez:
15
8
2022
Statut:
ppublish
Résumé
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. 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. although rarely reported, clinicians should still suspect and know how to manage such as rare and locally invasive tumor as a maxillary ameloblastoma. 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.
Identifiants
pubmed: 35969907
pii: S2210-2612(22)00703-9
doi: 10.1016/j.ijscr.2022.107457
pmc: PMC9400081
pii:
doi:
Types de publication
Case Reports
Langues
eng
Pagination
107457Informations de copyright
Copyright © 2022 The Author(s). Published by Elsevier Ltd.. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors report no declarations of interest.