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Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()

INTRODUCTION: Intraoral neurilemmomas (schwannoma) are rare, even rarer are intraosseous ones, and the rarest are the maxillary neurilemmomas. Going by the literature only 5 cases of maxillary neurilemomas are reported till now. Neurilemmomas are benign tumours of nerve sheath origin. Approximately...

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Autores principales: Verma, Ankit, Banerjee, Kinjal, Verma, Arpit, Singh, Sugandha, Rao, Jagdeep, Om, Prabha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825964/
https://www.ncbi.nlm.nih.gov/pubmed/24129122
http://dx.doi.org/10.1016/j.ijscr.2013.09.006
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author Verma, Ankit
Banerjee, Kinjal
Verma, Arpit
Singh, Sugandha
Rao, Jagdeep
Om, Prabha
author_facet Verma, Ankit
Banerjee, Kinjal
Verma, Arpit
Singh, Sugandha
Rao, Jagdeep
Om, Prabha
author_sort Verma, Ankit
collection PubMed
description INTRODUCTION: Intraoral neurilemmomas (schwannoma) are rare, even rarer are intraosseous ones, and the rarest are the maxillary neurilemmomas. Going by the literature only 5 cases of maxillary neurilemomas are reported till now. Neurilemmomas are benign tumours of nerve sheath origin. Approximately 30% arise in head and neck region, of these 1–12% arise intraorally mainly involving tongue. PRESENTATION OF CASE: Here we report two cases of maxillary neurilemmoma, one in a 9 year old girl and second one in a 27 year old female, both involving the lateral surface of maxilla on right side. Both the patients presented with a long standing history of swelling which was increasing gradually. 9-Year-old girl also had 1 lesion in the temporal region on right side and the 27-year-old patient had associated erosion of the soft palate. Diagnosis was made on the basis of histopathology and immunohistochemistry. DISCUSSION: Neurilemmomas are slow growing benign tumour of the nerve sheath origin arising from the Schwann cells. Their aetiology is not known. Most common complaint is that of a gradually increasing swelling followed by pain and paresthesias. Surgery remains the treatment of choice with close follow up. CONCLUSION: Maxillary neurilemmomas are rarest of the rare tumour which closely mimic benign odontogenic cysts and tumours, and should be kept in the differential diagnosis of these lesions. Knowledge of the radiologic and clinical behaviour of these tumours is extremely important for prompt diagnosis and treatment.
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spelling pubmed-38259642013-11-13 Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases() Verma, Ankit Banerjee, Kinjal Verma, Arpit Singh, Sugandha Rao, Jagdeep Om, Prabha Int J Surg Case Rep Article INTRODUCTION: Intraoral neurilemmomas (schwannoma) are rare, even rarer are intraosseous ones, and the rarest are the maxillary neurilemmomas. Going by the literature only 5 cases of maxillary neurilemomas are reported till now. Neurilemmomas are benign tumours of nerve sheath origin. Approximately 30% arise in head and neck region, of these 1–12% arise intraorally mainly involving tongue. PRESENTATION OF CASE: Here we report two cases of maxillary neurilemmoma, one in a 9 year old girl and second one in a 27 year old female, both involving the lateral surface of maxilla on right side. Both the patients presented with a long standing history of swelling which was increasing gradually. 9-Year-old girl also had 1 lesion in the temporal region on right side and the 27-year-old patient had associated erosion of the soft palate. Diagnosis was made on the basis of histopathology and immunohistochemistry. DISCUSSION: Neurilemmomas are slow growing benign tumour of the nerve sheath origin arising from the Schwann cells. Their aetiology is not known. Most common complaint is that of a gradually increasing swelling followed by pain and paresthesias. Surgery remains the treatment of choice with close follow up. CONCLUSION: Maxillary neurilemmomas are rarest of the rare tumour which closely mimic benign odontogenic cysts and tumours, and should be kept in the differential diagnosis of these lesions. Knowledge of the radiologic and clinical behaviour of these tumours is extremely important for prompt diagnosis and treatment. Elsevier 2013-09-21 /pmc/articles/PMC3825964/ /pubmed/24129122 http://dx.doi.org/10.1016/j.ijscr.2013.09.006 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Verma, Ankit
Banerjee, Kinjal
Verma, Arpit
Singh, Sugandha
Rao, Jagdeep
Om, Prabha
Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()
title Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()
title_full Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()
title_fullStr Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()
title_full_unstemmed Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()
title_short Maxillary neurilemmoma—Rarest of the rare tumour: Report of 2 cases()
title_sort maxillary neurilemmoma—rarest of the rare tumour: report of 2 cases()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3825964/
https://www.ncbi.nlm.nih.gov/pubmed/24129122
http://dx.doi.org/10.1016/j.ijscr.2013.09.006
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