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A rare case of nasal septal schwannoma: Case report and literature review

Introduction: Sinonasal schwannoma accounts for only 4% of head and neck nerve sheath tumors. Schwannoma of the nasal septum is still the rarest, with only few cases previously reported. Case presentation: This study presents the case of a 64-year-old Saudi female of the Eastern Province who present...

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Autores principales: Alrasheed, Wejdan, Almomen, Ali, Alkhatib, Abdulrahman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370567/
https://www.ncbi.nlm.nih.gov/pubmed/30738369
http://dx.doi.org/10.1016/j.ijscr.2019.01.027
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author Alrasheed, Wejdan
Almomen, Ali
Alkhatib, Abdulrahman
author_facet Alrasheed, Wejdan
Almomen, Ali
Alkhatib, Abdulrahman
author_sort Alrasheed, Wejdan
collection PubMed
description Introduction: Sinonasal schwannoma accounts for only 4% of head and neck nerve sheath tumors. Schwannoma of the nasal septum is still the rarest, with only few cases previously reported. Case presentation: This study presents the case of a 64-year-old Saudi female of the Eastern Province who presented a several-month history of unilateral progressive nasal obstruction and recurrent episodes of epistaxis. The diagnosis of nasal septal schwannoma was made on the basis of a histopathological examination. The case was managed successfully by endoscopic endonasal excision with no postoperative recurrence. Discussion: Nasal septal schwannoma is rare and has only 32 reported cases. Diagnosis primarily depends on histopathological examination. Endoscopic endonasal excision of the mass is considered the ideal treatment for such pathology. Conclusion: Schwannoma of the nasal septum is rare. However, it should be included as a differential diagnosis in a patient presenting with a unilateral nasal mass.
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spelling pubmed-63705672019-02-21 A rare case of nasal septal schwannoma: Case report and literature review Alrasheed, Wejdan Almomen, Ali Alkhatib, Abdulrahman Int J Surg Case Rep Article Introduction: Sinonasal schwannoma accounts for only 4% of head and neck nerve sheath tumors. Schwannoma of the nasal septum is still the rarest, with only few cases previously reported. Case presentation: This study presents the case of a 64-year-old Saudi female of the Eastern Province who presented a several-month history of unilateral progressive nasal obstruction and recurrent episodes of epistaxis. The diagnosis of nasal septal schwannoma was made on the basis of a histopathological examination. The case was managed successfully by endoscopic endonasal excision with no postoperative recurrence. Discussion: Nasal septal schwannoma is rare and has only 32 reported cases. Diagnosis primarily depends on histopathological examination. Endoscopic endonasal excision of the mass is considered the ideal treatment for such pathology. Conclusion: Schwannoma of the nasal septum is rare. However, it should be included as a differential diagnosis in a patient presenting with a unilateral nasal mass. Elsevier 2019-01-30 /pmc/articles/PMC6370567/ /pubmed/30738369 http://dx.doi.org/10.1016/j.ijscr.2019.01.027 Text en © 2019 The Authors http://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 Article
Alrasheed, Wejdan
Almomen, Ali
Alkhatib, Abdulrahman
A rare case of nasal septal schwannoma: Case report and literature review
title A rare case of nasal septal schwannoma: Case report and literature review
title_full A rare case of nasal septal schwannoma: Case report and literature review
title_fullStr A rare case of nasal septal schwannoma: Case report and literature review
title_full_unstemmed A rare case of nasal septal schwannoma: Case report and literature review
title_short A rare case of nasal septal schwannoma: Case report and literature review
title_sort rare case of nasal septal schwannoma: case report and literature review
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6370567/
https://www.ncbi.nlm.nih.gov/pubmed/30738369
http://dx.doi.org/10.1016/j.ijscr.2019.01.027
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