Friedrich Reinhard E, Reul Anika
Department of Oral and Craniomaxillofacial Surgery, Eppendorf University Hospital, University of Hamburg, HamburgGermany.
Department of Prosthodontics, Eppendorf University Hospital, University of Hamburg, HamburgGermany.
J Oral Maxillofac Res. 2017 Dec 31;8(4):e5. doi: 10.5037/jomr.2017.8405. eCollection 2017 Oct-Dec.
The purpose of the present study was the systematic investigation of numerical and morphological aberrations of teeth in the wisdom teeth region in neurofibromatosis type 1 patients.
The panoramic radiographs of 179 patients were analysed for supernumerary molars and dysplastic wisdom teeth with special reference to facial tumour type. The results were compared to radiographic findings obtained in panoramic radiographs of age- and sex-matched controls.
The total number of dysplastic or supernumerary molars was 21 (17 individuals, 4.75%) and predominantly a finding of the maxilla (maxilla: 15, mandible: 1, maxilla and mandible: 1). Differences of dental findings between neurofibromatosis type 1 (NF1) patients (n = 15) and the control group (n = 2) were statistically significant (P < 0.01). All individuals with supernumerary molars were diagnosed as being affected with NF1. This difference achieved statistical significance when it was considered that the event may occur at least once per quadrant, and thus the individual potentially needs to be considered four times (P = 0.0038).
This investigation revealed that supernumerary molars and aberrations in wisdom tooth form are more common in patients than in age- and sex-matched controls. There is no association between these findings and a specific feature of the disease, id est facial manifestation of a trigeminal nerve sheath tumour (plexiform neurofibroma). The cause of this phenomenon is unknown. A review of these dental findings on other neurofibromatosis type 1 study groups should be attempted.
本研究旨在系统调查1型神经纤维瘤病患者智齿区域牙齿的数量和形态异常情况。
分析179例患者的全景X线片,以确定多生磨牙和发育异常的智齿,并特别参考面部肿瘤类型。将结果与年龄和性别匹配的对照组全景X线片的影像学结果进行比较。
发育异常或多生磨牙的总数为21颗(17例患者,4.75%),主要见于上颌(上颌:15颗,下颌:1颗,上下颌均有:1颗)。1型神经纤维瘤病(NF1)患者(n = 15)和对照组(n = 2)的牙齿检查结果差异具有统计学意义(P < 0.01)。所有有多生磨牙的个体均被诊断为患有NF1。当考虑到该事件可能在每个象限至少发生一次,因此个体可能需要被考虑四次时,这种差异具有统计学意义(P = 0.0038)。
本研究表明,多生磨牙和智齿形态异常在患者中比在年龄和性别匹配的对照组中更为常见。这些发现与疾病的特定特征(即三叉神经鞘瘤(丛状神经纤维瘤)的面部表现)之间没有关联。这种现象的原因尚不清楚。应尝试对其他1型神经纤维瘤病研究组的这些牙齿检查结果进行综述。