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Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review

BACKGROUND: Ameloblastoma is a benign locally invasive lesion that represents 1% of all oral tumors. Epidemiological characteristics are variable in the literature. The most common origin sites are mandible and maxilla. Rarely presents metastasis, but the skull base, lymph nodes, and the lung are de...

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Autores principales: Ferreira, Tiago Silva Holanda, Pimentel, Isnara Mara Freitas, de Albuquerque, Lucas Alverne Freitas, Gondim, Jackson A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451162/
https://www.ncbi.nlm.nih.gov/pubmed/32874731
http://dx.doi.org/10.25259/SNI_45_2020
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author Ferreira, Tiago Silva Holanda
Pimentel, Isnara Mara Freitas
de Albuquerque, Lucas Alverne Freitas
Gondim, Jackson A.
author_facet Ferreira, Tiago Silva Holanda
Pimentel, Isnara Mara Freitas
de Albuquerque, Lucas Alverne Freitas
Gondim, Jackson A.
author_sort Ferreira, Tiago Silva Holanda
collection PubMed
description BACKGROUND: Ameloblastoma is a benign locally invasive lesion that represents 1% of all oral tumors. Epidemiological characteristics are variable in the literature. The most common origin sites are mandible and maxilla. Rarely presents metastasis, but the skull base, lymph nodes, and the lung are described as metastatic sites. Low recurrence rates were reported by the authors when surgical treatment achieved complete resection. CASE DESCRIPTION: A female patient, 19 years old presenting moderate headache associated with nausea, vomiting, left facial hypoesthesia, and low visual acuity. Resonance image showed a heterogeneous expansive solid formation in sphenoid bone and clivus with neoplastic aspect. Signs of dissemination due to contiguity and invasion of skull base structures, especially cavernous sinus and internal carotid artery, determining also compression of the brainstem. First, an endoscopic biopsy was performed with otorhinolaryngology service. The pathological study showed histological characteristics of ameloblastoma. After, the patient was submitted to endoscopic surgery for resection of tumor. CONCLUSION: Ameloblastoma is a rare tumor with benign behavior and slow growing. It arises from odontogenic epithelium and accounts 1% of all oral tumors. The mandible and maxilla are the most common sites of origin. Ameloblastoma with intracranial involvement is a rare presentation with few literature reviews. A long time illness course and multiple surgeries are characteristics present in the majority of cases described. Total resection surgery is the treatment of choice and endoscopic transnasal resection is a viable option.
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spelling pubmed-74511622020-08-31 Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review Ferreira, Tiago Silva Holanda Pimentel, Isnara Mara Freitas de Albuquerque, Lucas Alverne Freitas Gondim, Jackson A. Surg Neurol Int Case Report BACKGROUND: Ameloblastoma is a benign locally invasive lesion that represents 1% of all oral tumors. Epidemiological characteristics are variable in the literature. The most common origin sites are mandible and maxilla. Rarely presents metastasis, but the skull base, lymph nodes, and the lung are described as metastatic sites. Low recurrence rates were reported by the authors when surgical treatment achieved complete resection. CASE DESCRIPTION: A female patient, 19 years old presenting moderate headache associated with nausea, vomiting, left facial hypoesthesia, and low visual acuity. Resonance image showed a heterogeneous expansive solid formation in sphenoid bone and clivus with neoplastic aspect. Signs of dissemination due to contiguity and invasion of skull base structures, especially cavernous sinus and internal carotid artery, determining also compression of the brainstem. First, an endoscopic biopsy was performed with otorhinolaryngology service. The pathological study showed histological characteristics of ameloblastoma. After, the patient was submitted to endoscopic surgery for resection of tumor. CONCLUSION: Ameloblastoma is a rare tumor with benign behavior and slow growing. It arises from odontogenic epithelium and accounts 1% of all oral tumors. The mandible and maxilla are the most common sites of origin. Ameloblastoma with intracranial involvement is a rare presentation with few literature reviews. A long time illness course and multiple surgeries are characteristics present in the majority of cases described. Total resection surgery is the treatment of choice and endoscopic transnasal resection is a viable option. Scientific Scholar 2020-08-01 /pmc/articles/PMC7451162/ /pubmed/32874731 http://dx.doi.org/10.25259/SNI_45_2020 Text en Copyright: © 2020 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Ferreira, Tiago Silva Holanda
Pimentel, Isnara Mara Freitas
de Albuquerque, Lucas Alverne Freitas
Gondim, Jackson A.
Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review
title Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review
title_full Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review
title_fullStr Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review
title_full_unstemmed Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review
title_short Pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: Case report and literature review
title_sort pure endoscopic transsphenoidal treatment of skull base ameloblastoma with intracranial extension: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7451162/
https://www.ncbi.nlm.nih.gov/pubmed/32874731
http://dx.doi.org/10.25259/SNI_45_2020
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