口腔底骨软骨性脉络瘤1例

IF 0.4 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Takasuke Usuki , Soju Seki , Toshihiro Uchihashi , Tomonori Sasahira , Shingo Kodama , Kohei Kawamura , Susumu Tanaka , Syoichiro Ishii , Munehiro Hamaguchi
{"title":"口腔底骨软骨性脉络瘤1例","authors":"Takasuke Usuki ,&nbsp;Soju Seki ,&nbsp;Toshihiro Uchihashi ,&nbsp;Tomonori Sasahira ,&nbsp;Shingo Kodama ,&nbsp;Kohei Kawamura ,&nbsp;Susumu Tanaka ,&nbsp;Syoichiro Ishii ,&nbsp;Munehiro Hamaguchi","doi":"10.1016/j.ajoms.2025.05.003","DOIUrl":null,"url":null,"abstract":"<div><div><span>Osteocartilaginous choristomas<span><span> are benign bone lesion<span> composed of hyaline cartilage that undergo ossification and arise when osteochondral cells proliferate into surrounding tissues. In the oral and maxillofacial regions, these lesions usually occur on the dorsum of the </span></span>tongue<span>, with no reported cases of osteocartilaginous choristomas occurring on the oral floor. We report the case of a 57-year-old Japanese male referred to our hospital in late November 2021 with the chief complaint of tongue hypoaesthesia and a mass on the right side of the oral floor. Clinical examination revealed that the lesion was a 22 × 13 mm elastic hard mass with an ulcer at the centre of the lesion on the right side of the oral floor behind Walton's canal orifice. Computed tomography images showed an opaque mass with a major diameter of 20 mm, internal heterogeneity, and a well-defined border located slightly to the right of the floor of the </span></span></span>oral cavity<span>. Surgical resection was performed through an intraoral incision<span> under local anaesthesia. The imaging and surgical findings at our hospital showed a 22 × 15 mm lesion with clear boundaries, which could be removed as a single mass from the surrounding connective tissue. Histological investigation revealed that lesion has the characteristics of hyaline cartilage with some areas showing ossification, leading to a diagnosis of osteocartilaginous choristoma of the oral floor. The patient has progressed well and remains recurrence-free 2 years postoperatively.</span></span></div></div>","PeriodicalId":45034,"journal":{"name":"Journal of Oral and Maxillofacial Surgery Medicine and Pathology","volume":"37 6","pages":"Pages 1299-1303"},"PeriodicalIF":0.4000,"publicationDate":"2025-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A case of osteocartilaginous choristoma at the floor of the oral cavity\",\"authors\":\"Takasuke Usuki ,&nbsp;Soju Seki ,&nbsp;Toshihiro Uchihashi ,&nbsp;Tomonori Sasahira ,&nbsp;Shingo Kodama ,&nbsp;Kohei Kawamura ,&nbsp;Susumu Tanaka ,&nbsp;Syoichiro Ishii ,&nbsp;Munehiro Hamaguchi\",\"doi\":\"10.1016/j.ajoms.2025.05.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><span>Osteocartilaginous choristomas<span><span> are benign bone lesion<span> composed of hyaline cartilage that undergo ossification and arise when osteochondral cells proliferate into surrounding tissues. In the oral and maxillofacial regions, these lesions usually occur on the dorsum of the </span></span>tongue<span>, with no reported cases of osteocartilaginous choristomas occurring on the oral floor. We report the case of a 57-year-old Japanese male referred to our hospital in late November 2021 with the chief complaint of tongue hypoaesthesia and a mass on the right side of the oral floor. Clinical examination revealed that the lesion was a 22 × 13 mm elastic hard mass with an ulcer at the centre of the lesion on the right side of the oral floor behind Walton's canal orifice. Computed tomography images showed an opaque mass with a major diameter of 20 mm, internal heterogeneity, and a well-defined border located slightly to the right of the floor of the </span></span></span>oral cavity<span>. Surgical resection was performed through an intraoral incision<span> under local anaesthesia. The imaging and surgical findings at our hospital showed a 22 × 15 mm lesion with clear boundaries, which could be removed as a single mass from the surrounding connective tissue. Histological investigation revealed that lesion has the characteristics of hyaline cartilage with some areas showing ossification, leading to a diagnosis of osteocartilaginous choristoma of the oral floor. The patient has progressed well and remains recurrence-free 2 years postoperatively.</span></span></div></div>\",\"PeriodicalId\":45034,\"journal\":{\"name\":\"Journal of Oral and Maxillofacial Surgery Medicine and Pathology\",\"volume\":\"37 6\",\"pages\":\"Pages 1299-1303\"},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2025-05-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Oral and Maxillofacial Surgery Medicine and Pathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2212555825000900\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral and Maxillofacial Surgery Medicine and Pathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2212555825000900","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

摘要

骨软骨瘤是一种由透明软骨组成的良性骨病变,当骨软骨细胞增生到周围组织时发生骨化。在口腔和颌面区域,这些病变通常发生在舌背,没有报道的病例骨软骨性脉络瘤发生在口腔底。我们报告一例于2021年11月下旬转诊至我院的57岁日本男性患者,其主诉为舌头感觉减退和口腔底部右侧肿块。临床检查显示病变为22 × 13 mm的弹性硬块,病变中心位于沃尔顿管口后的口腔底部右侧。计算机断层扫描图像显示一个不透明的肿块,直径为20 mm,内部不均匀,边界清晰,位于口腔底部略右侧。在局部麻醉下通过口内切口进行手术切除。本院影像学及手术表现为22 × 15 mm病灶,边界清晰,可作为单个肿块从周围结缔组织切除。组织学检查显示病变具有透明软骨的特征,部分区域显示骨化,因此诊断为口腔底骨软骨性脉络瘤。患者进展良好,术后2年无复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of osteocartilaginous choristoma at the floor of the oral cavity
Osteocartilaginous choristomas are benign bone lesion composed of hyaline cartilage that undergo ossification and arise when osteochondral cells proliferate into surrounding tissues. In the oral and maxillofacial regions, these lesions usually occur on the dorsum of the tongue, with no reported cases of osteocartilaginous choristomas occurring on the oral floor. We report the case of a 57-year-old Japanese male referred to our hospital in late November 2021 with the chief complaint of tongue hypoaesthesia and a mass on the right side of the oral floor. Clinical examination revealed that the lesion was a 22 × 13 mm elastic hard mass with an ulcer at the centre of the lesion on the right side of the oral floor behind Walton's canal orifice. Computed tomography images showed an opaque mass with a major diameter of 20 mm, internal heterogeneity, and a well-defined border located slightly to the right of the floor of the oral cavity. Surgical resection was performed through an intraoral incision under local anaesthesia. The imaging and surgical findings at our hospital showed a 22 × 15 mm lesion with clear boundaries, which could be removed as a single mass from the surrounding connective tissue. Histological investigation revealed that lesion has the characteristics of hyaline cartilage with some areas showing ossification, leading to a diagnosis of osteocartilaginous choristoma of the oral floor. The patient has progressed well and remains recurrence-free 2 years postoperatively.
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
CiteScore
0.80
自引率
0.00%
发文量
129
审稿时长
83 days
×
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:604180095
Book学术官方微信