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A rare case of primary sinonasal meningioma: A case report

INTRODUCTION AND IMPORTANCE: Extra cranial primary meningioma of sinonasal tract is a rare entity. It is often misdiagnosed as nasal polyp. CASE PRESENTATION: Here we report a case of a primary ethmoid sinus meningioma with extension into the nasal cavity in a 41-year-old man. The tumor was complete...

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Autores principales: Abir, Meherzi, Rihab, Lahmar, Bellakhdhar, Mouna, Malika, Omri, Jihen, Hwass, Wassim, Kermani, Abdelkefi, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568705/
https://www.ncbi.nlm.nih.gov/pubmed/36122423
http://dx.doi.org/10.1016/j.ijscr.2022.107620
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author Abir, Meherzi
Rihab, Lahmar
Bellakhdhar, Mouna
Malika, Omri
Jihen, Hwass
Wassim, Kermani
Abdelkefi, Mohamed
author_facet Abir, Meherzi
Rihab, Lahmar
Bellakhdhar, Mouna
Malika, Omri
Jihen, Hwass
Wassim, Kermani
Abdelkefi, Mohamed
author_sort Abir, Meherzi
collection PubMed
description INTRODUCTION AND IMPORTANCE: Extra cranial primary meningioma of sinonasal tract is a rare entity. It is often misdiagnosed as nasal polyp. CASE PRESENTATION: Here we report a case of a primary ethmoid sinus meningioma with extension into the nasal cavity in a 41-year-old man. The tumor was completely excised via endoscopic endonasalapproach and the histologic diagnosis of meningioma was established. The patient was regularly follow up for 12 months without recurrence of the tumor. CLINICAL DISCUSSION: The final diagnosis of primary sinonasal meningioma is based on histopathology and immunohistochemistry analyses results. The importance of complete surgical resection is undoubted and also is a goodindicator prognosis. CONCLUSION: The otolaryngologists should be aware of the diagnosis of primary meningioma; despite of its rarity it is considered as a possible cause of nasal obstruction.
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spelling pubmed-95687052022-10-16 A rare case of primary sinonasal meningioma: A case report Abir, Meherzi Rihab, Lahmar Bellakhdhar, Mouna Malika, Omri Jihen, Hwass Wassim, Kermani Abdelkefi, Mohamed Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Extra cranial primary meningioma of sinonasal tract is a rare entity. It is often misdiagnosed as nasal polyp. CASE PRESENTATION: Here we report a case of a primary ethmoid sinus meningioma with extension into the nasal cavity in a 41-year-old man. The tumor was completely excised via endoscopic endonasalapproach and the histologic diagnosis of meningioma was established. The patient was regularly follow up for 12 months without recurrence of the tumor. CLINICAL DISCUSSION: The final diagnosis of primary sinonasal meningioma is based on histopathology and immunohistochemistry analyses results. The importance of complete surgical resection is undoubted and also is a goodindicator prognosis. CONCLUSION: The otolaryngologists should be aware of the diagnosis of primary meningioma; despite of its rarity it is considered as a possible cause of nasal obstruction. Elsevier 2022-09-09 /pmc/articles/PMC9568705/ /pubmed/36122423 http://dx.doi.org/10.1016/j.ijscr.2022.107620 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Abir, Meherzi
Rihab, Lahmar
Bellakhdhar, Mouna
Malika, Omri
Jihen, Hwass
Wassim, Kermani
Abdelkefi, Mohamed
A rare case of primary sinonasal meningioma: A case report
title A rare case of primary sinonasal meningioma: A case report
title_full A rare case of primary sinonasal meningioma: A case report
title_fullStr A rare case of primary sinonasal meningioma: A case report
title_full_unstemmed A rare case of primary sinonasal meningioma: A case report
title_short A rare case of primary sinonasal meningioma: A case report
title_sort rare case of primary sinonasal meningioma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9568705/
https://www.ncbi.nlm.nih.gov/pubmed/36122423
http://dx.doi.org/10.1016/j.ijscr.2022.107620
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