下颌骨孤立性骨内神经纤维瘤:病例报告

Amir Jalal Abbasi, P. Aminishakib, M. Arashrad
{"title":"下颌骨孤立性骨内神经纤维瘤:病例报告","authors":"Amir Jalal Abbasi, P. Aminishakib, M. Arashrad","doi":"10.18502/jcr.v10i4.15314","DOIUrl":null,"url":null,"abstract":"Neurofibroma is a benign tumor derived from the peripheral nerve. Most of these can be multifocal as a component of neurofibromatosis or present as a solitary tumor. Although the solitary neurofibroma is not an uncommon lesion, its intraosseous occurrence is rare, and less than 50 cases have been reported. \nWe report a rare case of central neurofibroma, arising in the mandibular bone of 57-year-old edentulous female patient on the left side. Hemi mandibulectomy was performed and reconstructed with a reconstruction plate without any bone graft. Microscopic evaluation showed neoplastic tissue with haphazardly arranged and interlacing fascicular patterns composed of point-ended spindle-shaped tumoral cells. Immunohistochemical examination of the tumor showed positive staining for S-100 protein antibodies.","PeriodicalId":52622,"journal":{"name":"Journal of Craniomaxillofacial Research","volume":"59 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Solitary Intraosseous Neurofibroma of Mandible: Report of a Case\",\"authors\":\"Amir Jalal Abbasi, P. Aminishakib, M. Arashrad\",\"doi\":\"10.18502/jcr.v10i4.15314\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Neurofibroma is a benign tumor derived from the peripheral nerve. Most of these can be multifocal as a component of neurofibromatosis or present as a solitary tumor. Although the solitary neurofibroma is not an uncommon lesion, its intraosseous occurrence is rare, and less than 50 cases have been reported. \\nWe report a rare case of central neurofibroma, arising in the mandibular bone of 57-year-old edentulous female patient on the left side. Hemi mandibulectomy was performed and reconstructed with a reconstruction plate without any bone graft. Microscopic evaluation showed neoplastic tissue with haphazardly arranged and interlacing fascicular patterns composed of point-ended spindle-shaped tumoral cells. Immunohistochemical examination of the tumor showed positive staining for S-100 protein antibodies.\",\"PeriodicalId\":52622,\"journal\":{\"name\":\"Journal of Craniomaxillofacial Research\",\"volume\":\"59 6\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Craniomaxillofacial Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18502/jcr.v10i4.15314\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Craniomaxillofacial Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18502/jcr.v10i4.15314","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

神经纤维瘤是一种源自周围神经的良性肿瘤。大多数神经纤维瘤可作为神经纤维瘤病的一个组成部分而多发,也可表现为单发肿瘤。虽然单发性神经纤维瘤并非罕见病变,但其在骨内的发生率却很低,目前报道的病例不到 50 例。我们报告了一例罕见的中央型神经纤维瘤病例,该病例发生在 57 岁无牙女性患者的下颌骨左侧。患者接受了下颌骨半切除术,并在不植骨的情况下用重建板进行了重建。显微镜检查显示,肿瘤组织由点状纺锤形肿瘤细胞组成,呈杂乱排列和交错的束状。肿瘤的免疫组化检查显示,S-100 蛋白抗体呈阳性染色。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Solitary Intraosseous Neurofibroma of Mandible: Report of a Case
Neurofibroma is a benign tumor derived from the peripheral nerve. Most of these can be multifocal as a component of neurofibromatosis or present as a solitary tumor. Although the solitary neurofibroma is not an uncommon lesion, its intraosseous occurrence is rare, and less than 50 cases have been reported. We report a rare case of central neurofibroma, arising in the mandibular bone of 57-year-old edentulous female patient on the left side. Hemi mandibulectomy was performed and reconstructed with a reconstruction plate without any bone graft. Microscopic evaluation showed neoplastic tissue with haphazardly arranged and interlacing fascicular patterns composed of point-ended spindle-shaped tumoral cells. Immunohistochemical examination of the tumor showed positive staining for S-100 protein antibodies.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
8
审稿时长
12 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信