Familial multiple impacted supernumerary teeth: Case report.

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Journal of International Medical Research Pub Date : 2025-06-01 Epub Date: 2025-06-16 DOI:10.1177/03000605251339146
Loulwah K Alothman, Azizah F Bin Mubayrik, Reema Alshawaf, Randa Alfotawi, Abdulaziz S Alqahtani
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引用次数: 0

Abstract

Multiple impacted supernumerary teeth are rare and need a multidisciplinary approach for optimal management to reduce potential complications. Herein, we present the case of an otherwise generally healthy woman in her early 30s who presented to the oral medicine clinic with a chief complaint of multiple missing teeth. Family history revealed that her sister and brother had the same complaint. Panoramic and cone-beam computed tomography radiographic findings revealed the presence of multiple impacted supernumerary teeth in both jaws. Multiple radiopacities and frontal sinus osteoma were noted. The radiographic features were suggestive of Gardner syndrome. An endoscopy was requested, which turned out negative for any polyps, with a recommendation to repeat endoscopy after 10 years. This is because the cranial osteoma might precede the gastrointestinal polyposis. A comprehensive treatment plan was performed by a team of dentists from multiple specialties (oral medicine, oral radiology, orthodontics, prosthodontics, and oral surgery) to ensure optimal outcomes for the patient. Thus, it is essential for dentists to identify and explore any atypical findings that may arise during clinical examination.

家族性多埋伏多生牙1例。
多埋伏多生牙是罕见的,需要多学科的方法来优化管理,以减少潜在的并发症。在这里,我们提出的情况下,一般健康的妇女在她的30岁出头,谁提出了口腔医学诊所多颗牙齿缺失的主诉。家族史显示她的姐姐和哥哥也有同样的症状。全景和锥束计算机断层扫描结果显示双颌存在多颗阻生多牙。多发放射性阴影及额窦骨瘤。x线表现提示Gardner综合征。要求进行内窥镜检查,结果显示没有任何息肉,并建议10年后再次进行内窥镜检查。这是因为颅骨瘤可能先于胃肠道息肉病。由来自多个专业(口腔医学、口腔放射学、正畸学、修复学和口腔外科)的牙医团队执行综合治疗计划,以确保患者获得最佳结果。因此,牙医必须识别和探索临床检查中可能出现的任何非典型发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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