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Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature
BACKGROUND: Neurofibromas are benign tumors of a neurogenic origin. If these tumors occur without any other signs of neurofibromatosis, they are classified as isolated neurofibromas. Neurofibromas in the oral cavity mostly occur within soft tissues, indicating that solitary intraosseous neurofibroma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600983/ https://www.ncbi.nlm.nih.gov/pubmed/37900249 http://dx.doi.org/10.12998/wjcc.v11.i27.6653 |
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author | Zhang, Zheng Hong, Xia Wang, Feng Ye, Xin Yao, You-Dan Yin, Ying Yang, Hong-Yu |
author_facet | Zhang, Zheng Hong, Xia Wang, Feng Ye, Xin Yao, You-Dan Yin, Ying Yang, Hong-Yu |
author_sort | Zhang, Zheng |
collection | PubMed |
description | BACKGROUND: Neurofibromas are benign tumors of a neurogenic origin. If these tumors occur without any other signs of neurofibromatosis, they are classified as isolated neurofibromas. Neurofibromas in the oral cavity mostly occur within soft tissues, indicating that solitary intraosseous neurofibromas in the mandible are rare. Due to the absence of specific clinical manifestations, early diagnosis and treatment of these tumors are difficult to achieve. CASE SUMMARY: A 37-year-old female patient visited our hospital due to numbness and swelling of the gums in the right lower molar area that had persisted for half a month. The patient’s overall condition and intraoral examination revealed no significant abnormalities. She was initially diagnosed with a cystic lesion in the right mandible. However, after a more thorough examination, the final pathological diagnosis was confirmed to be neurofibroma. Complete tumor resection and partial removal of the right inferior alveolar nerve were performed. As of writing this report, there have been no signs of tumor recurrence for nine months following the surgery. CONCLUSION: This case report discusses the key features that are useful for differentiating solitary intraosseous neurofibromas from other cystic lesions. |
format | Online Article Text |
id | pubmed-10600983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-106009832023-10-27 Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature Zhang, Zheng Hong, Xia Wang, Feng Ye, Xin Yao, You-Dan Yin, Ying Yang, Hong-Yu World J Clin Cases Case Report BACKGROUND: Neurofibromas are benign tumors of a neurogenic origin. If these tumors occur without any other signs of neurofibromatosis, they are classified as isolated neurofibromas. Neurofibromas in the oral cavity mostly occur within soft tissues, indicating that solitary intraosseous neurofibromas in the mandible are rare. Due to the absence of specific clinical manifestations, early diagnosis and treatment of these tumors are difficult to achieve. CASE SUMMARY: A 37-year-old female patient visited our hospital due to numbness and swelling of the gums in the right lower molar area that had persisted for half a month. The patient’s overall condition and intraoral examination revealed no significant abnormalities. She was initially diagnosed with a cystic lesion in the right mandible. However, after a more thorough examination, the final pathological diagnosis was confirmed to be neurofibroma. Complete tumor resection and partial removal of the right inferior alveolar nerve were performed. As of writing this report, there have been no signs of tumor recurrence for nine months following the surgery. CONCLUSION: This case report discusses the key features that are useful for differentiating solitary intraosseous neurofibromas from other cystic lesions. Baishideng Publishing Group Inc 2023-09-26 2023-09-26 /pmc/articles/PMC10600983/ /pubmed/37900249 http://dx.doi.org/10.12998/wjcc.v11.i27.6653 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Case Report Zhang, Zheng Hong, Xia Wang, Feng Ye, Xin Yao, You-Dan Yin, Ying Yang, Hong-Yu Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature |
title | Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature |
title_full | Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature |
title_fullStr | Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature |
title_full_unstemmed | Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature |
title_short | Solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: A case report and review of literature |
title_sort | solitary intraosseous neurofibroma in the mandible mimicking a cystic lesion: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600983/ https://www.ncbi.nlm.nih.gov/pubmed/37900249 http://dx.doi.org/10.12998/wjcc.v11.i27.6653 |
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