Odontogenic myxofibroma arising in the mandibular angle of a child with long-term follow-up: A case report

Tumor discovery Pub Date : 2024-03-19 DOI:10.36922/td.2096
Momoko Yoshikawa, T. Karube, Hiroki Nagamine, W. Muraoka, Hideki Kizu, H. Kawana, T. Nakagawa, S. Asoda
{"title":"Odontogenic myxofibroma arising in the mandibular angle of a child with long-term follow-up: A case report","authors":"Momoko Yoshikawa, T. Karube, Hiroki Nagamine, W. Muraoka, Hideki Kizu, H. Kawana, T. Nakagawa, S. Asoda","doi":"10.36922/td.2096","DOIUrl":null,"url":null,"abstract":"Odontogenic myxofibroma of the jawbone is a rarity in children, and there are few reports of cases with long-term follow-up, which mainly describe the growth process of odontogenic myxofibroma. We herein report a case of odontogenic myxofibroma that arose in the mandibular angle of a pediatric patient with a long-term follow-up of more than 14 years. The patient, when he was 10-years-old, first approached us with a complaint of painless swelling in the right mandibular angle that was palpable and showed bone-like hardness. Computed tomography revealed an ill-defined bone defect measuring 20 mm in diameter with bone protrusion in the margin. A biopsy was performed to differentiate the mass from osteosarcoma, giving a preliminary diagnosis of odontogenic myxofibroma or chondromyxofibroma. Therefore, tumorectomy was performed under general anesthesia. We curetted the bone surrounding the tumor and filled defect with iliac cancellous bone. The final diagnosis was odontogenic myxofibroma. At present, 14 years after the surgery, the patient had experienced an uneventful post-operative course without recurrence.","PeriodicalId":94260,"journal":{"name":"Tumor discovery","volume":"59 40","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Tumor discovery","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.36922/td.2096","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Odontogenic myxofibroma of the jawbone is a rarity in children, and there are few reports of cases with long-term follow-up, which mainly describe the growth process of odontogenic myxofibroma. We herein report a case of odontogenic myxofibroma that arose in the mandibular angle of a pediatric patient with a long-term follow-up of more than 14 years. The patient, when he was 10-years-old, first approached us with a complaint of painless swelling in the right mandibular angle that was palpable and showed bone-like hardness. Computed tomography revealed an ill-defined bone defect measuring 20 mm in diameter with bone protrusion in the margin. A biopsy was performed to differentiate the mass from osteosarcoma, giving a preliminary diagnosis of odontogenic myxofibroma or chondromyxofibroma. Therefore, tumorectomy was performed under general anesthesia. We curetted the bone surrounding the tumor and filled defect with iliac cancellous bone. The final diagnosis was odontogenic myxofibroma. At present, 14 years after the surgery, the patient had experienced an uneventful post-operative course without recurrence.
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
一名儿童下颌角的牙源性肌纤维瘤及长期随访:病例报告
颌骨的牙源性肌纤维瘤在儿童中较为罕见,长期随访的病例报道很少,主要描述的是牙源性肌纤维瘤的生长过程。我们在此报告了一例发生在儿童患者下颌角的牙源性肌纤维瘤,该病例经过了超过 14 年的长期随访。患者 10 岁时首次就诊,主诉右下颌角出现无痛性肿胀,可触及并显示骨样硬度。计算机断层扫描显示,该处有一个直径为 20 毫米的界限不清的骨缺损,边缘有骨突起。为了将肿块与骨肉瘤区分开来,医生对肿块进行了活检,初步诊断为牙源性肌纤维瘤或软骨性肌纤维瘤。因此,在全身麻醉下进行了肿瘤切除术。我们刮除了肿瘤周围的骨头,并用髂骨松质骨填充了缺损。最终诊断为牙源性肌纤维瘤。目前,手术已过去 14 年,患者术后恢复顺利,没有复发。
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
Matrix metalloproteinase-1 as a potential biomarker for early gastric cancer detection and its effect on gastric cancer cell proliferation and migration Bioinformatics analysis of missense mutations in CXCR1 implicates altered protein stability and function Profiling energy metabolism in normal bladder tissue and non-muscle-invasive bladder cancer cases of different histological grades Odontogenic myxofibroma arising in the mandibular angle of a child with long-term follow-up: A case report Artificial intelligence enabled spatially resolved transcriptomics reveal spatial tissue organization of multiple tumors
×
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