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Le polype sphénochoanal: une entité rare avec revue de la littérature

Sphenochoanal polyp is a rare form of choanal polyp originating from the sphenoid sinus and extending to the choanae via the sphenoethmoidal recess. We report a case of sphenochoanal polyp in a 15-year-old boy presenting with a 3-year history of chronic progressive nasal obstruction, treated with en...

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Autores principales: Houda, Mounji, Salk, Eddafi, Malika, Benfdil, Mehdi, Elfakiri, Youssef, Rochdi, Hassan, Nouri, Abdelaziz, Raji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757228/
https://www.ncbi.nlm.nih.gov/pubmed/33425172
http://dx.doi.org/10.11604/pamj.2020.37.139.20832
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author Houda, Mounji
Salk, Eddafi
Malika, Benfdil
Mehdi, Elfakiri
Youssef, Rochdi
Hassan, Nouri
Abdelaziz, Raji
author_facet Houda, Mounji
Salk, Eddafi
Malika, Benfdil
Mehdi, Elfakiri
Youssef, Rochdi
Hassan, Nouri
Abdelaziz, Raji
author_sort Houda, Mounji
collection PubMed
description Sphenochoanal polyp is a rare form of choanal polyp originating from the sphenoid sinus and extending to the choanae via the sphenoethmoidal recess. We report a case of sphenochoanal polyp in a 15-year-old boy presenting with a 3-year history of chronic progressive nasal obstruction, treated with endoscopic surgery with good post-operative outcome. Sphenochoanal polyp is extremely rare. Symptomatically, it resembles an antrochoanal polyp. Adequate preoperative evaluation based on endoscopic examination and computed tomography (CT) scan or magnetic resonance imaging is necessary for accurate diagnosis and appropriate surgical strategy. Endoscopic excision is the treatment of choice.
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spelling pubmed-77572282021-01-07 Le polype sphénochoanal: une entité rare avec revue de la littérature Houda, Mounji Salk, Eddafi Malika, Benfdil Mehdi, Elfakiri Youssef, Rochdi Hassan, Nouri Abdelaziz, Raji Pan Afr Med J Case Report Sphenochoanal polyp is a rare form of choanal polyp originating from the sphenoid sinus and extending to the choanae via the sphenoethmoidal recess. We report a case of sphenochoanal polyp in a 15-year-old boy presenting with a 3-year history of chronic progressive nasal obstruction, treated with endoscopic surgery with good post-operative outcome. Sphenochoanal polyp is extremely rare. Symptomatically, it resembles an antrochoanal polyp. Adequate preoperative evaluation based on endoscopic examination and computed tomography (CT) scan or magnetic resonance imaging is necessary for accurate diagnosis and appropriate surgical strategy. Endoscopic excision is the treatment of choice. The African Field Epidemiology Network 2020-10-08 /pmc/articles/PMC7757228/ /pubmed/33425172 http://dx.doi.org/10.11604/pamj.2020.37.139.20832 Text en Copyright: Mounji Houda et al. https://creativecommons.org/licenses/by/4.0 The Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Houda, Mounji
Salk, Eddafi
Malika, Benfdil
Mehdi, Elfakiri
Youssef, Rochdi
Hassan, Nouri
Abdelaziz, Raji
Le polype sphénochoanal: une entité rare avec revue de la littérature
title Le polype sphénochoanal: une entité rare avec revue de la littérature
title_full Le polype sphénochoanal: une entité rare avec revue de la littérature
title_fullStr Le polype sphénochoanal: une entité rare avec revue de la littérature
title_full_unstemmed Le polype sphénochoanal: une entité rare avec revue de la littérature
title_short Le polype sphénochoanal: une entité rare avec revue de la littérature
title_sort le polype sphénochoanal: une entité rare avec revue de la littérature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757228/
https://www.ncbi.nlm.nih.gov/pubmed/33425172
http://dx.doi.org/10.11604/pamj.2020.37.139.20832
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