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Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review

Sinonasal ameloblastoma (SNA) is considered to be a subtype of ameloblastoma. It differs from gnathic ameloblastoma in terms of clinicopathologic features, management and prognosis. Thus, the objective of the present review was to study the complications, survival, recurrence rate and outcomes follo...

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Autores principales: Mehta, Vini, Sarode, Gargi S., Obulareddy, Vishnu Teja, Sharma, Tanvi, Kokane, Shruti, Cicciù, Marco, Minervini, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821057/
https://www.ncbi.nlm.nih.gov/pubmed/36615180
http://dx.doi.org/10.3390/jcm12010381
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author Mehta, Vini
Sarode, Gargi S.
Obulareddy, Vishnu Teja
Sharma, Tanvi
Kokane, Shruti
Cicciù, Marco
Minervini, Giuseppe
author_facet Mehta, Vini
Sarode, Gargi S.
Obulareddy, Vishnu Teja
Sharma, Tanvi
Kokane, Shruti
Cicciù, Marco
Minervini, Giuseppe
author_sort Mehta, Vini
collection PubMed
description Sinonasal ameloblastoma (SNA) is considered to be a subtype of ameloblastoma. It differs from gnathic ameloblastoma in terms of clinicopathologic features, management and prognosis. Thus, the objective of the present review was to study the complications, survival, recurrence rate and outcomes following the management of SNA. The electronic search process was conducted on PubMed-Medline, Embase, and Scopus. Google Scholar was used to search grey literature. Quality assessment of the case reports (CR) and case series (CS) was done based on CARE guidelines. The initial search resulted in 2111 articles. 15 studies (13 CR and 2 CS) were found to meet the eligibility criteria. The majority of the studies described histological features of SNA, which were consistent with ameloblastomas of gnathic origin. There were no SNA-related deaths reported in the included studies. Five studies described endoscopic surgeries to remove SNAs, and three SNAs were treated with post-surgery radiotherapy. Data from included studies suggest that sinonasal ameloblastomas are histologically similar to gnathic ameloblastomas, but their clinical presentation is different. They may cause complete or partial obstruction of the nasal cavity and the sinus. They appear to affect an older demographic, and their resection may be accompanied by the excision of a large portion of the maxilla, necessitating maxillofacial prosthetic rehabilitation.
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spelling pubmed-98210572023-01-07 Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review Mehta, Vini Sarode, Gargi S. Obulareddy, Vishnu Teja Sharma, Tanvi Kokane, Shruti Cicciù, Marco Minervini, Giuseppe J Clin Med Systematic Review Sinonasal ameloblastoma (SNA) is considered to be a subtype of ameloblastoma. It differs from gnathic ameloblastoma in terms of clinicopathologic features, management and prognosis. Thus, the objective of the present review was to study the complications, survival, recurrence rate and outcomes following the management of SNA. The electronic search process was conducted on PubMed-Medline, Embase, and Scopus. Google Scholar was used to search grey literature. Quality assessment of the case reports (CR) and case series (CS) was done based on CARE guidelines. The initial search resulted in 2111 articles. 15 studies (13 CR and 2 CS) were found to meet the eligibility criteria. The majority of the studies described histological features of SNA, which were consistent with ameloblastomas of gnathic origin. There were no SNA-related deaths reported in the included studies. Five studies described endoscopic surgeries to remove SNAs, and three SNAs were treated with post-surgery radiotherapy. Data from included studies suggest that sinonasal ameloblastomas are histologically similar to gnathic ameloblastomas, but their clinical presentation is different. They may cause complete or partial obstruction of the nasal cavity and the sinus. They appear to affect an older demographic, and their resection may be accompanied by the excision of a large portion of the maxilla, necessitating maxillofacial prosthetic rehabilitation. MDPI 2023-01-03 /pmc/articles/PMC9821057/ /pubmed/36615180 http://dx.doi.org/10.3390/jcm12010381 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Systematic Review
Mehta, Vini
Sarode, Gargi S.
Obulareddy, Vishnu Teja
Sharma, Tanvi
Kokane, Shruti
Cicciù, Marco
Minervini, Giuseppe
Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review
title Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review
title_full Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review
title_fullStr Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review
title_full_unstemmed Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review
title_short Clinicopathologic Profile, Management and Outcome of Sinonasal Ameloblastoma—A Systematic Review
title_sort clinicopathologic profile, management and outcome of sinonasal ameloblastoma—a systematic review
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821057/
https://www.ncbi.nlm.nih.gov/pubmed/36615180
http://dx.doi.org/10.3390/jcm12010381
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