Neurofibromatosis Type 1 in the Mandible

Neurofibromatosis type 1 (NF1) was first described in 1882 as a hamartomatous disorder of neural crest derivation. We present the imaging of a 65-year-old woman with NF1. Computed tomography revealed that there were three major findings presented: skeletal deformity, an area of fat (probably related...

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Autores principales: Uchiyama, Yuka, Sumi, Tetsuro, Marutani, Keisuke, Takaoka, Hiroo, Murakami, Shumei, Kameyama, Hiroyasu, Yura, Yoshiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report - Tumors
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018268/
https://www.ncbi.nlm.nih.gov/pubmed/29963437
http://dx.doi.org/10.4103/ams.ams_135_17
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author Uchiyama, Yuka
Sumi, Tetsuro
Marutani, Keisuke
Takaoka, Hiroo
Murakami, Shumei
Kameyama, Hiroyasu
Yura, Yoshiaki
author_facet Uchiyama, Yuka
Sumi, Tetsuro
Marutani, Keisuke
Takaoka, Hiroo
Murakami, Shumei
Kameyama, Hiroyasu
Yura, Yoshiaki
author_sort Uchiyama, Yuka
collection PubMed
description Neurofibromatosis type 1 (NF1) was first described in 1882 as a hamartomatous disorder of neural crest derivation. We present the imaging of a 65-year-old woman with NF1. Computed tomography revealed that there were three major findings presented: skeletal deformity, an area of fat (probably related to mesodermal dysplasia), and benign neoplasm within the masticator space. Moreover, masticatory muscles were hypoplastic.
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spelling pubmed-60182682018-06-29 Neurofibromatosis Type 1 in the Mandible Uchiyama, Yuka Sumi, Tetsuro Marutani, Keisuke Takaoka, Hiroo Murakami, Shumei Kameyama, Hiroyasu Yura, Yoshiaki Ann Maxillofac Surg Case Report - Tumors Neurofibromatosis type 1 (NF1) was first described in 1882 as a hamartomatous disorder of neural crest derivation. We present the imaging of a 65-year-old woman with NF1. Computed tomography revealed that there were three major findings presented: skeletal deformity, an area of fat (probably related to mesodermal dysplasia), and benign neoplasm within the masticator space. Moreover, masticatory muscles were hypoplastic. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6018268/ /pubmed/29963437 http://dx.doi.org/10.4103/ams.ams_135_17 Text en Copyright: © 2018 Annals of Maxillofacial Surgery http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report - Tumors
Uchiyama, Yuka
Sumi, Tetsuro
Marutani, Keisuke
Takaoka, Hiroo
Murakami, Shumei
Kameyama, Hiroyasu
Yura, Yoshiaki
Neurofibromatosis Type 1 in the Mandible
title Neurofibromatosis Type 1 in the Mandible
title_full Neurofibromatosis Type 1 in the Mandible
title_fullStr Neurofibromatosis Type 1 in the Mandible
title_full_unstemmed Neurofibromatosis Type 1 in the Mandible
title_short Neurofibromatosis Type 1 in the Mandible
title_sort neurofibromatosis type 1 in the mandible
topic Case Report - Tumors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018268/
https://www.ncbi.nlm.nih.gov/pubmed/29963437
http://dx.doi.org/10.4103/ams.ams_135_17
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AT kameyamahiroyasu neurofibromatosistype1inthemandible
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