| Literature DB >> 33401498 |
Saverio Capodiferro1, Luisa Limongelli1, Silvia D'Agostino2, Angela Tempesta1, Marco Dolci2, Eugenio Maiorano3, Gianfranco Favia1.
Abstract
Juvenile nasopharyngeal angiofibroma is a rare vascular neoplasm, mostly occurring in adolescent males, and representing 0.05% of all head and neck tumors. Nevertheless, it is usually recognized as the most common benign mesenchymal neoplasm of the nasopharynx. Usually, it originates from the posterolateral wall of the nasopharynx and, although histologically benign, classically shows a locally aggressive behavior with bone destruction as well as spreading through natural foramina and/or fissures to the nasopharynx, nasal and paranasal cavities, spheno-palatine foramen, infratemporal fossa and, very rarely, to the cranial cavity. Extranasopharyngeal angiofibroma is considered a distinct entity due to older age at presentation, different localizations (outside the nasopharyngeal pterygopalatine fossa) and attenuated clinical course. Extranasopharyngeal angiofibroma has been sporadically described in the oral cavity. We report a case of extranasopharyngeal angiofibroma with primary and exclusive involvement of the adherent gingiva of the anterior maxilla, managed by preoperative diode laser trans-mucosal photocoagulation and subsequent surgical removal. The current literature on primary extranasopharyngeal angiofibroma is also reviewed.Entities:
Keywords: diode laser; extranasopharyngeal angiofibroma; nasopharyngeal angiofibroma; oral cavity; trans-mucosal photocoagulation
Year: 2021 PMID: 33401498 PMCID: PMC7824373 DOI: 10.3390/healthcare9010033
Source DB: PubMed Journal: Healthcare (Basel) ISSN: 2227-9032