Wotjiuk Fabienne, Hyon Isabelle, Dajean-Trutaud Sylvie, Badran Zahi, Prud'homme Tony
Prosthetic Dentistry Department, CHU/Université Nantes, France.
Pediatric Dentistry Department, CHU/Université Nantes, France.
Int J Clin Pediatr Dent. 2019 Nov-Dec;12(6):577-581. doi: 10.5005/jp-journals-10005-1668.
Neurofibromatosis type 1 (NF1) is a clinically heterogeneous neurocutaneous genetic disorder that manifests in the form of coffee-milk spots on the skin, Lish nodules, lentigines on the underarms and on the inguinal region, and neurofibromas. Orofacial manifestations of NF1 are common. Through a review of the literature, bone lesions, orthodontic and dental abnormalities, periodontal manifestations, and caries related to NF1 will be explored. In this study, we present a clinical case of a patient with neurofibroma in the oral cavity and infraocclusion of primary molars, as well as his dental management.
Wotjiuk F, Hyon I, Dajean-Trutaud S, Dental Management of Neurofibromatosis Type 1: A Case Report and Literature Review. Int J Clin Pediatr Dent 2019;12(6):577-581.
1型神经纤维瘤病(NF1)是一种临床异质性神经皮肤遗传性疾病,表现为皮肤上的牛奶咖啡斑、Lisch结节、腋窝和腹股沟区的雀斑以及神经纤维瘤。NF1的口腔面部表现很常见。通过文献回顾,将探讨与NF1相关的骨病变、正畸和牙齿异常、牙周表现以及龋齿。在本研究中,我们报告了一例口腔内有神经纤维瘤且乳牙低位咬合的患者的临床病例及其牙科治疗情况。
Wotjiuk F, Hyon I, Dajean-Trutaud S, 1型神经纤维瘤病的牙科治疗:病例报告及文献回顾。《国际临床儿科牙科杂志》2019年;12(6):577 - 581。