A lateral cephalometry study of patients with neurofibromatosis type 1

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A lateral cephalometry study of patients with neurofibromatosis type 1. / Friedrich, Reinhard E; Lehmann, Jan-Marten; Rother, Jonathan; Christ, Georg; Zu Eulenburg, Christine; Scheuer, Hannah T; Scheuer, Hanna A.

in: J CRANIO MAXILL SURG, Jahrgang 45, Nr. 6, 06.2017, S. 809-820.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Friedrich, RE, Lehmann, J-M, Rother, J, Christ, G, Zu Eulenburg, C, Scheuer, HT & Scheuer, HA 2017, 'A lateral cephalometry study of patients with neurofibromatosis type 1', J CRANIO MAXILL SURG, Jg. 45, Nr. 6, S. 809-820. https://doi.org/10.1016/j.jcms.2017.02.011

APA

Friedrich, R. E., Lehmann, J-M., Rother, J., Christ, G., Zu Eulenburg, C., Scheuer, H. T., & Scheuer, H. A. (2017). A lateral cephalometry study of patients with neurofibromatosis type 1. J CRANIO MAXILL SURG, 45(6), 809-820. https://doi.org/10.1016/j.jcms.2017.02.011

Vancouver

Friedrich RE, Lehmann J-M, Rother J, Christ G, Zu Eulenburg C, Scheuer HT et al. A lateral cephalometry study of patients with neurofibromatosis type 1. J CRANIO MAXILL SURG. 2017 Jun;45(6):809-820. https://doi.org/10.1016/j.jcms.2017.02.011

Bibtex

@article{1560dc58adb844d08516d3d8aa8d4a52,
title = "A lateral cephalometry study of patients with neurofibromatosis type 1",
abstract = "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.",
keywords = "Journal Article",
author = "Friedrich, {Reinhard E} and Jan-Marten Lehmann and Jonathan Rother and Georg Christ and {Zu Eulenburg}, Christine and Scheuer, {Hannah T} and Scheuer, {Hanna A}",
note = "Copyright {\textcopyright} 2017 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.",
year = "2017",
month = jun,
doi = "10.1016/j.jcms.2017.02.011",
language = "English",
volume = "45",
pages = "809--820",
journal = "J CRANIO MAXILL SURG",
issn = "1010-5182",
publisher = "Elsevier",
number = "6",

}

RIS

TY - JOUR

T1 - A lateral cephalometry study of patients with neurofibromatosis type 1

AU - Friedrich, Reinhard E

AU - Lehmann, Jan-Marten

AU - Rother, Jonathan

AU - Christ, Georg

AU - Zu Eulenburg, Christine

AU - Scheuer, Hannah T

AU - Scheuer, Hanna A

N1 - Copyright © 2017 European Association for Cranio-Maxillo-Facial Surgery. Published by Elsevier Ltd. All rights reserved.

PY - 2017/6

Y1 - 2017/6

N2 - 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.

AB - 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.

KW - Journal Article

U2 - 10.1016/j.jcms.2017.02.011

DO - 10.1016/j.jcms.2017.02.011

M3 - SCORING: Journal article

C2 - 28365079

VL - 45

SP - 809

EP - 820

JO - J CRANIO MAXILL SURG

JF - J CRANIO MAXILL SURG

SN - 1010-5182

IS - 6

ER -