Psammomatoid juvenile ossifying fibroma of the mandible with secondary aneurysmal bone cyst: A case report

Pushkar Waknis , Sachin C. Sarode , R.S. Dolas
{"title":"Psammomatoid juvenile ossifying fibroma of the mandible with secondary aneurysmal bone cyst: A case report","authors":"Pushkar Waknis ,&nbsp;Sachin C. Sarode ,&nbsp;R.S. Dolas","doi":"10.1016/j.ajoms.2010.12.001","DOIUrl":null,"url":null,"abstract":"<div><p>Juvenile psammomatoid ossifying fibroma (JPOF) is a rare, slowly progressive tumor of the extragnathic craniofacial bones, with a tendency towards locally aggressive behavior and recurrence. The pathognomonic histopathologic feature is the presence of spherical ossicles, which are similar to psammoma bodies. Very few cases in association with secondary aneurysmal bone cyst (ABC) formation have been reported in the literature. Treatment consists of complete surgical removal and incomplete excision has been associated with a high local recurrence rate. The prognosis is good because malignant change and metastasis have not been reported. Authors report a case of JPOF of the mandible with secondary ABC in a 17-year-old male patient.</p></div>","PeriodicalId":100128,"journal":{"name":"Asian Journal of Oral and Maxillofacial Surgery","volume":"23 2","pages":"Pages 83-86"},"PeriodicalIF":0.0000,"publicationDate":"2011-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.ajoms.2010.12.001","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Oral and Maxillofacial Surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0915699210001299","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 12

Abstract

Juvenile psammomatoid ossifying fibroma (JPOF) is a rare, slowly progressive tumor of the extragnathic craniofacial bones, with a tendency towards locally aggressive behavior and recurrence. The pathognomonic histopathologic feature is the presence of spherical ossicles, which are similar to psammoma bodies. Very few cases in association with secondary aneurysmal bone cyst (ABC) formation have been reported in the literature. Treatment consists of complete surgical removal and incomplete excision has been associated with a high local recurrence rate. The prognosis is good because malignant change and metastasis have not been reported. Authors report a case of JPOF of the mandible with secondary ABC in a 17-year-old male patient.

青少年下颌骨沙瘤样骨化纤维瘤伴继发性动脉瘤性骨囊肿1例
幼年沙砾样骨化纤维瘤(JPOF)是一种罕见的,缓慢进展的颅面骨外肿瘤,具有局部侵袭性和复发的倾向。病理组织学特征是球形小骨的存在,类似沙砾瘤体。文献中很少报道继发性动脉瘤性骨囊肿(ABC)形成的病例。治疗包括完全手术切除,不完全切除与高局部复发率有关。由于未见恶性改变和转移的报道,预后良好。作者报告了一个17岁男性患者下颌骨JPOF伴继发性ABC的病例。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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