Yuzi Kamiya, Hidetaka Narita, Tadashi Yamamoto, Yoichiro Kameyama , Hatsuhiko Maeda, Satoshi Nakane
{"title":"Familial odontogenic keratocysts","authors":"Yuzi Kamiya,&nbsp;Hidetaka Narita,&nbsp;Tadashi Yamamoto,&nbsp;Yoichiro Kameyama ,&nbsp;Hatsuhiko Maeda,&nbsp;Satoshi Nakane","doi":"10.1016/S0300-9785(85)80013-2","DOIUrl":null,"url":null,"abstract":"<div><p>Familial odontogenic keratocysts are described in this report. The Case 1 patient, who has 3 sisters, developed odontogenic keratocysts. The 2 younger sisters (Cases 2 and 3) also had odontogenic keratocysts, although the elder sister did not have any odontogenic cysts. The father of the patients had a history of removal of a jaw cyst, and the mother was found later to have malignant ameloblastoma. Besides the odontogenic keratocysts, the Case 1 patient had basal cell nevus, prominent frontal process, and ocular hypertelorism; the Case 2 patient had prominent frontal process; the Case 3 patient had prominent frontal process, ocular hypertelorism, and squint. All 3 sisters are suspected of being patients with the basal cell nevus syndrome. The Japanese dental literature concerning the basal cell nevus syndrome is reviewed.</p></div>","PeriodicalId":14224,"journal":{"name":"International journal of oral surgery","volume":"14 1","pages":"Pages 73-80"},"PeriodicalIF":0.0000,"publicationDate":"1985-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0300-9785(85)80013-2","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of oral surgery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0300978585800132","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

摘要

本报告描述家族性牙源性角化囊肿。病例1患者有3个姐妹,发生牙源性角化囊肿。2个妹妹(病例2和3)也有牙源性角化囊肿,尽管姐姐没有任何牙源性囊肿。患者的父亲有颌囊肿切除史,母亲后来被发现患有恶性成釉细胞瘤。除牙源性角化囊肿外,病例1还伴有基底细胞痣、额突突出和远视;病例2患者额突突出;病例3患者有突出的额突、远视和斜视。三姐妹均怀疑为基底细胞痣综合征患者。本文回顾了日本有关基底细胞痣综合征的牙科文献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Familial odontogenic keratocysts

Familial odontogenic keratocysts are described in this report. The Case 1 patient, who has 3 sisters, developed odontogenic keratocysts. The 2 younger sisters (Cases 2 and 3) also had odontogenic keratocysts, although the elder sister did not have any odontogenic cysts. The father of the patients had a history of removal of a jaw cyst, and the mother was found later to have malignant ameloblastoma. Besides the odontogenic keratocysts, the Case 1 patient had basal cell nevus, prominent frontal process, and ocular hypertelorism; the Case 2 patient had prominent frontal process; the Case 3 patient had prominent frontal process, ocular hypertelorism, and squint. All 3 sisters are suspected of being patients with the basal cell nevus syndrome. The Japanese dental literature concerning the basal cell nevus syndrome is reviewed.

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
0
期刊最新文献
A case of large cell neuroendocrine carcinoma of the tongue Application of microendosurgery for extensive radicular cysts A case of epidermoid cyst arising in the left side of the root of the tongue A case of posterior open bite after bilateral coronoidectomy and aponeurectomy of the masseter muscles Development of standards for stored autologous blood transfunction. Adaptation to orthognathic surgery.:Adaptation to orthognathic surgery
×
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