当超常牙齿的数量过多时,毛细血管畸形综合症的诊断就有了新的选择。

Pub Date : 2024-10-16 eCollection Date: 2024-01-01 DOI:10.1155/2024/2630240
Nariman Shaker, Aya Abdelrady, Sara F A Haridy, Waleed El-Beialy
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引用次数: 0

摘要

背景:在现代牙科实践中,多生牙的发病率越来越高。然而,对于多颗编外牙的存在应进行进一步调查。通过早期诊断和最佳随访筛查,对潜在综合征的正确诊断可使患者免于未来的健康危害。病例介绍:一名 13 岁的女性患者因多颗乳牙滞留和恒牙萌出延迟而就诊。虽然患者的病史和家族史没有引起任何关注,但临床和放射学检查却发现了令人费解的问题。患者共有 11 颗超常牙齿,除了存在滞留的乳牙外,还阻碍了恒牙的正常萌出。鉴于该病例的复杂性,医生对其进行了更多的临床和实验室检查,最终确诊为三尖瓣畸形综合征(TRPS)I 型。患者接受了精确的治疗方案,术后随访 6 个月,以监测恒牙的萌出情况。结论当综合征是根本原因时,监测异常病例,如多颗超常牙齿的病例,可以挽救生命或帮助早期诊断更严重的并发症。
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When an Overwhelming Number of Supernumerary Teeth Provides an Alternative to the Diagnosis of Trichorhinophalangeal Syndrome.

Background: The prevalence of supernumerary teeth is increasing in modern dental practice. However, the presence of multiple supernumerary teeth should be further investigated. Proper diagnosis of an underlying syndrome might save the patient from future health hazards through early diagnosis and optimal follow-up screening. Case Presentation: A 13-year-old female patient presented with multiple retained deciduous teeth and delayed eruption of permanent teeth. Although the medical and family history of the patient did not raise any concerns, the clinical and radiographic examinations yielded intriguing findings. The patient presented with a total of 11 supernumerary teeth, which impeded the normal eruption of permanent dentition in addition to the presence of retained deciduous teeth. Additional clinical and laboratory investigations were conducted in response to the case's complexity, resulting in the diagnosis of Trichorhinophalangeal Syndrome (TRPS) Type I. The patient underwent a precise treatment plan and then was followed up for 6 months postoperatively to monitor the eruptive movement of the permanent teeth. Conclusion: When a syndrome is the underlying cause, monitoring unusual cases, such as those with multiple supernumerary teeth, can be lifesaving or aid in the early diagnosis of more serious complications.

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