A lateral cephalometry study of patients with neurofibromatosis type 1

被引:14
|
作者
Friedrich, Reinhard E. [1 ,4 ]
Lehmann, Jan-Marten [1 ,4 ]
Rother, Jonathan [1 ,4 ]
Christ, Georg [1 ,4 ]
zu Eulenburg, Christine [2 ]
Scheuer, Hannah T. [4 ]
Scheuer, Hanna A. [3 ]
机构
[1] Univ Hamburg, Eppendorf Univ Hosp, Oral & Craniomaxillofacial Surg, Hamburg, Germany
[2] Univ Hamburg, Eppendorf Univ Hosp, Inst Epidemiol & Biometry, Hamburg, Germany
[3] Univ Hamburg, Eppendorf Univ Hosp, Orthodont, Hamburg, Germany
[4] Neurofibromatosis Lab, Hamburg, Germany
关键词
Neurofibromatosis type 1; Cephalometry; Plexiform neurofibroma; Craniofacial anomalies; PLEXIFORM NEUROFIBROMAS; DESCRIPTIVE ANALYSIS; ORBITAL DYSPLASIA; NF1; CHILDREN; RADIOGRAPHS; DEFORMITIES; MANAGEMENT; DIAGNOSIS; DELETIONS;
D O I
10.1016/j.jcms.2017.02.011
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: Neurofibromatosis type 1 (NF1) is an autosomal dominant transmitted tumour suppressor syndrome and also a bone disease. Osseous dysplasia affecting the craniofacial region is characteristic of NF1. The aim of this study was to analyse the lateral cephalograms of NF1 patients in comparison to individuals who were not affected by this condition in order to describe the skeletal phenotype of NF1 in more detail. Materials and methods: The study comprises the lateral cephalograms of 172 patients with established NF1 diagnoses (female = 85, male = 87). NF1 patients were distinguished by radiological and/or histological findings of the facial region suggestive of plexiform neurofibroma (PNF) or disseminated cutaneous NF (DNF). The analysed radiographs of a collection of 29 healthy volunteers with ideal occlusion served as controls. The focus of this analysis was cephalometrically defined angles. Results: Cephalometric analyses of patients with DNF did not differ from those of controls for the vast majority of parameters. However, the measurement results of patients with PNF differed significantly from those of healthy volunteers and patients with DNF. The number of trigeminal nerve branches affected in PNF patients had an effect on the measurement results. Conclusion: Lateral cephalograms revealed no significant alteration of the facial skeleton in NF1 patients as compared to controls. Indeed, the stigma of a so-called 'NF1 facies' cannot be derived from the cephalometric findings presented. Notably, a wide range of deviating readings were recorded for individuals with facial PNF. Clinicians who treat patients with NF1 should be aware of deviations from cephalometric standards on lateral cephalograms in NF1 patients, especially when craniofacial surgical procedures are planned. Some of these findings, particularly asymmetries of the facial skeleton, could be indicators of an associated PNF. (C) 2017 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:809 / 820
页数:12
相关论文
共 50 条
  • [1] Sphenoid Bone Pneumatisation on Lateral Cephalograms of Patients With Neurofibromatosis Type 1
    Friedrich, Reinhard E.
    Scheuer, Hannah T.
    Kersten, Jan F.
    Scheuer, Hanna A.
    IN VIVO, 2021, 35 (01): : 349 - 361
  • [2] Malignancies in Chinese patients with neurofibromatosis type 1
    Cheuk, Daniel K. L.
    Chiang, Alan K. S.
    Ha, S. Y.
    Chan, Godfrey C. F.
    HONG KONG MEDICAL JOURNAL, 2013, 19 (01) : 42 - 49
  • [3] Spinal Surgery in Patients with Type-1 Neurofibromatosis: A Comprehensive Review
    Joaquim, Andrei Fernandes
    BRAZILIAN NEUROSURGERY-ARQUIVOS BRASILEIROS DE NEUROCIRURGIA, 2023, 42 (02): : 152 - 159
  • [4] Spinal manifestations of Neurofibromatosis type 1
    Shofty, Ben
    Barzilai, Ori
    Khashan, Morsi
    Lidar, Zvi
    Constantini, Shlomi
    CHILDS NERVOUS SYSTEM, 2020, 36 (10) : 2401 - 2408
  • [5] Craniofacial bone alterations in patients with neurofibromatosis type 1
    Chauvel-Picard, Julie
    Lion-Francois, Laurence
    Beuriat, Pierre-Aurelien
    Paulus, Christian
    Szathmari, Alexandru
    Mottolese, Carmine
    Gleizal, Arnaud
    Di Rocco, Federico
    CHILDS NERVOUS SYSTEM, 2020, 36 (10) : 2391 - 2399
  • [6] Epidemiological profile and clinical characteristics of 491 Brazilian patients with neurofibromatosis type 1
    Darrigo Junior, Luiz Guilherme
    Ferraz, Victor Evangelista de Faria
    Cormedi, Marina Candido Visontai
    Araujo, Luissa Hikari Hayashi
    Magalhaes, Mariana Prado Silva
    Carneiro, Rafaella Curis
    Sales, Luis Henrique Nunes
    Suchmacher, Mendel
    Cunha, Karin Soares
    Filho, Aguinaldo Bonalumi
    Azulay, David Rubem
    Geller, Mauro
    BRAIN AND BEHAVIOR, 2022, 12 (06):
  • [7] Gliomas in patients with neurofibromatosis type 1
    Albers, Anne C.
    Gutmann, David H.
    EXPERT REVIEW OF NEUROTHERAPEUTICS, 2009, 9 (04) : 535 - 539
  • [8] Neuro-oncology of neurofibromatosis type 1
    Hottinger, Andreas F.
    Khakoo, Yasmin
    CURRENT TREATMENT OPTIONS IN NEUROLOGY, 2009, 11 (04) : 306 - 314
  • [9] Vitamin D and Bone Metabolism in Adult Patients with Neurofibromatosis Type 1
    Modica, Roberta
    Altieri, Barbara
    D'Aniello, Francesco
    Benevento, Elio
    Cannavale, Giuseppe
    Minotta, Roberto
    Liccardi, Alessia
    Colao, Annamaria
    Faggiano, Antongiulio
    METABOLITES, 2023, 13 (02)
  • [10] Growth and Pubertal Development of Neurofibromatosis Type 1 Patients
    Oliveira, Catia Priscila
    Santos-Silva, Rita
    Fontoura, Manuel
    REVISTA PORTUGUESA DE ENDOCRINOLOGIA DIABETES E METABOLISMO, 2019, 14 (02) : 180 - 186