Friedrich Reinhard E, Schön Moritz
Department of Oral and Craniomaxillofacial Surgery, Eppendorf University Hospital, University of Hamburg, Hamburg, Germany.
J Clin Exp Dent. 2024 Mar 1;16(3):e300-e322. doi: 10.4317/jced.61363. eCollection 2024 Mar.
Neurofibromatosis type 1 (NF1) is an autosomal dominant inherited tumor predisposition disease with a highly variable phenotype. The influence of the characteristic NF1 tumors (neurofibromas) on dentition has not yet been examined in detail. The aim of the study was to assess the dentition of NF1 children and adolescents, considering the symmetry of tooth development.
The panoramic radiographs of 59 patients with a confirmed NF1 diagnosis were compared with 59 age-and-sex-matched controls. The stages of tooth development on the sides of the jaw, added to a score, were assessed. In addition, the number of filled or decayed teeth, and the number of retained or missing teeth were assessed.
The tooth development of both study groups is symmetrical for almost all parameters and in the same developmental stage according to the sum score of the tooth development stages. Discrete developmental delays of teeth, in particular in the oral area of facial plexiform neurofibroma (PNF) are noticeable. NF1 patients' teeth showed less decay and more restorations than that of the control group. The facial PNF (FPNF) does not impair emergence of deciduous teeth.
Development of dentition of NF1 patients does not differ from the general population. However, FPNF with oral tumor components often prevent mesial movement of permanent molars and premolars, so these teeth do not develop contact (spacing), hardly emerge or may stay retained in bone. Oral PNF may have a low-retarding effect on some tooth root development (e.g., wisdom teeth). This effect is negligible when comparing the affected and unaffected sides of the jaw and is probably non-specific. Neurofibromatosis type 1, plexiform neurofibroma, dentition, mixed dentition, symmetry, oral health, tooth development.
1型神经纤维瘤病(NF1)是一种常染色体显性遗传的肿瘤易感性疾病,其表型具有高度变异性。特征性的NF1肿瘤(神经纤维瘤)对牙列的影响尚未得到详细研究。本研究的目的是在考虑牙齿发育对称性的情况下,评估NF1儿童和青少年的牙列情况。
将59例确诊为NF1的患者的全景X线片与59例年龄和性别匹配的对照者进行比较。评估颌骨两侧牙齿发育阶段,并计入分数。此外,评估已充填或龋坏牙齿的数量,以及滞留或缺失牙齿的数量。
根据牙齿发育阶段的总分,两个研究组的牙齿发育在几乎所有参数上都是对称的,且处于相同的发育阶段。牙齿存在离散性发育延迟,特别是在面部丛状神经纤维瘤(PNF)的口腔区域较为明显。NF1患者的牙齿龋坏较少,修复体比对照组更多。面部PNF(FPNF)不影响乳牙萌出。
NF1患者的牙列发育与一般人群没有差异。然而,伴有口腔肿瘤成分的FPNF常常阻碍恒牙磨牙和前磨牙的近中移动,因此这些牙齿无法形成接触(间隙),很难萌出或可能滞留在骨内。口腔PNF可能对某些牙根发育(如智齿)有轻度延迟作用。与颌骨的患侧和未患侧相比,这种影响可以忽略不计,且可能是非特异性的。1型神经纤维瘤病、丛状神经纤维瘤、牙列、混合牙列、对称性、口腔健康、牙齿发育。