Primary malignant fibrous histiocytoma of the mandible: Report of a rare case with an immunohistochemical analysis

Takaaki Kamatani , Akihisa Horie , Hiroaki Ishii , Hideo Kasahara , Yoshiki Hamada , Yoshio Aida , Satoru Shintani
{"title":"Primary malignant fibrous histiocytoma of the mandible: Report of a rare case with an immunohistochemical analysis","authors":"Takaaki Kamatani ,&nbsp;Akihisa Horie ,&nbsp;Hiroaki Ishii ,&nbsp;Hideo Kasahara ,&nbsp;Yoshiki Hamada ,&nbsp;Yoshio Aida ,&nbsp;Satoru Shintani","doi":"10.1016/j.ajoms.2010.04.003","DOIUrl":null,"url":null,"abstract":"<div><p>We present a rare case of a malignant fibrous histiocytoma (MFH) arising in the mandible of a 74-year-old Japanese woman. Intraoral examination revealed a single ulcer in the right mandibular alveolar ridge at the molar region. Panoramic radiographs revealed ill-defined radiopaque, radiolucent area in the right molar region. Computed tomography demonstrated a mass with cortical bone destruction. The histological examination revealed numerous fibroblast-like spindle-shaped cells arranged in a fascicular pattern and scattered multinucleated and mononuclear cells with bizarre nuclei throughout the lesion. Moderate nuclear pleomorphism was evident with few mitotic cells. The immunohistochemical techniques proved positive for vimentin of all tumor cells and Ki-67 of about half of the tumor cells and negative for c-kit, CD34, smooth muscle actin, CD68, S100 protein, and Factor VIII of all tumor cells. The lesion was diagnosed as a MFH of storiform-pleomorphic type. After surgical removal of the lesion and the adjacent tissues, the patient was referred to a radiotherapist for continuation of treatment and remains well almost a year later.</p></div>","PeriodicalId":100128,"journal":{"name":"Asian Journal of Oral and Maxillofacial Surgery","volume":"22 4","pages":"Pages 212-215"},"PeriodicalIF":0.0000,"publicationDate":"2010-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ajoms.2010.04.003","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Oral and Maxillofacial Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0915699210000919","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

Abstract

We present a rare case of a malignant fibrous histiocytoma (MFH) arising in the mandible of a 74-year-old Japanese woman. Intraoral examination revealed a single ulcer in the right mandibular alveolar ridge at the molar region. Panoramic radiographs revealed ill-defined radiopaque, radiolucent area in the right molar region. Computed tomography demonstrated a mass with cortical bone destruction. The histological examination revealed numerous fibroblast-like spindle-shaped cells arranged in a fascicular pattern and scattered multinucleated and mononuclear cells with bizarre nuclei throughout the lesion. Moderate nuclear pleomorphism was evident with few mitotic cells. The immunohistochemical techniques proved positive for vimentin of all tumor cells and Ki-67 of about half of the tumor cells and negative for c-kit, CD34, smooth muscle actin, CD68, S100 protein, and Factor VIII of all tumor cells. The lesion was diagnosed as a MFH of storiform-pleomorphic type. After surgical removal of the lesion and the adjacent tissues, the patient was referred to a radiotherapist for continuation of treatment and remains well almost a year later.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
下颌骨原发性恶性纤维组织细胞瘤:罕见病例报告及免疫组织化学分析
我们提出一个罕见的恶性纤维组织细胞瘤(MFH)出现在一个74岁的日本妇女下颌骨。口腔内检查显示右下颌牙槽嵴臼齿区有单一溃疡。全景x线片显示右侧磨牙区不透明、透光区。计算机断层扫描显示皮质骨破坏肿块。组织学检查显示大量成纤维细胞样纺锤状细胞呈束状排列,分散的多核和单核细胞,细胞核奇异。中度核多形性明显,有丝分裂细胞较少。免疫组化检测结果显示,所有肿瘤细胞的vimentin和Ki-67均呈阳性,而所有肿瘤细胞的c-kit、CD34、平滑肌肌动蛋白、CD68、S100蛋白和因子VIII均呈阴性。病变诊断为故事型-多形型MFH。手术切除病变和邻近组织后,患者被转介到放射治疗继续治疗,并在近一年后保持健康。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
WITHDRAWN: Juvenile psammomatoid ossifying fibroma of maxilla causing dysarthria, dysphagia and dyspnoea Editorial Board Oral and Maxillofacial Surgeons: The common Indian's knowledge about us Successful total mandibular reconstruction using a fibular graft with long-term follow-up: A case report A case of spindle cell carcinoma of the tongue metastasized to the thyroid gland
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1