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14 例原发性免疫缺陷病患者的口腔颌面部异常:临床和影像学分析及综述。

Dental anomalies in 14 patients with IP: clinical and radiological analysis and review.

机构信息

Postgraduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.

Postgraduate Program in Genetics and Molecular Biology, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

出版信息

Clin Oral Investig. 2017 Jun;21(5):1845-1852. doi: 10.1007/s00784-016-1977-y. Epub 2016 Oct 20.

Abstract

OBJECTIVES

Current knowledge on dental anomalies in patients with incontinentia pigmenti (IP) has been obtained by examining case reports; however, an overall characterization of such alterations remains lacking. The objective of this study was to determine the frequency, type and location of dental alterations in IP using a case series.

METHODS

Fourteen patients (9 children and 5 adults) with a clinical diagnosis of IP who presented dental anomalies were included in this study. All patients were administered a clinical questionnaire, dental examination and radiological investigation.

RESULTS

In the present case series, agenesis of primary dentition was present in 60 % of patients and agenesis of permanent tooth was present in 92.8 % of patients. Most cases were missing at least 6 teeth. Second molar agenesis was present in 13 patients (92.8 %). Anomalies in dental crowns occurred in 71.4 % of cases, and the central incisor was most frequently affected. Two adult patients still had primary teeth. Malocclusion was found in 10 patients (71.4 %). High-arched palate was observed in 7 (50 %) patients.

CONCLUSIONS

Patients with IP present alterations in both primary and permanent dentition. Because the agenesis of permanent teeth is more common, primary teeth are not always replaced. In addition, the durability of primary dentition appears to be greater in IP.

CLINICAL SIGNIFICANCE

This study shows that patients with IP experience significant loss of teeth, especially in permanent dentition, and have an increased risk of high-arched palate compared to the general population. Prophylactic care of primary teeth in IP is relevant for improving functional and aesthetic outcomes until dental prostheses are implanted.

摘要

目的

目前对于罹患色素失禁症(IP)患者的牙齿异常的了解主要来源于病例报告,然而,对于此类异常的全面描述仍存在缺失。本研究的目的是通过病例系列研究来确定 IP 患者的牙齿改变的频率、类型和位置。

方法

本研究纳入了 14 名(9 名儿童和 5 名成人)具有 IP 临床诊断且存在牙齿异常的患者。所有患者均接受了临床问卷调查、口腔检查和影像学检查。

结果

在本病例系列中,60%的患者存在乳牙缺失,92.8%的患者存在恒牙缺失。大多数患者至少缺失 6 颗牙齿。13 名患者(92.8%)存在第二磨牙缺失。71.4%的病例存在牙冠异常,且中切牙最常受累。2 名成年患者仍有乳牙。10 名患者(71.4%)存在错合畸形。10 名患者(71.4%)存在高拱形腭。

结论

IP 患者的乳牙和恒牙均存在改变。由于恒牙缺失更为常见,乳牙并不总是被替换。此外,IP 患者的乳牙似乎更耐用。

临床意义

本研究表明,与普通人群相比,IP 患者牙齿缺失的情况更为严重,尤其是恒牙缺失,且发生高拱形腭的风险更高。对 IP 患者的乳牙进行预防性护理对于改善功能和美观效果很重要,直到植入牙假体。

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