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Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient

Neurofibromatosis type I (NF1) is a neurocutaneous disorder that involves autosomal dominant transmission. Skull defects, including sphenoid dysplasia and calvarial defects, are a rare finding in patients with NF1. Spinal meningocele and sphenoid wing dysplasia have been identified in NF1 but the oc...

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Detalles Bibliográficos
Autores principales: Serindere, Mehmet, Tasar, Mustafa, Hamcan, Salih, Bozlar, Ugur
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757098/
https://www.ncbi.nlm.nih.gov/pubmed/29435380
http://dx.doi.org/10.1155/2017/7047696
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author Serindere, Mehmet
Tasar, Mustafa
Hamcan, Salih
Bozlar, Ugur
author_facet Serindere, Mehmet
Tasar, Mustafa
Hamcan, Salih
Bozlar, Ugur
author_sort Serindere, Mehmet
collection PubMed
description Neurofibromatosis type I (NF1) is a neurocutaneous disorder that involves autosomal dominant transmission. Skull defects, including sphenoid dysplasia and calvarial defects, are a rare finding in patients with NF1. Spinal meningocele and sphenoid wing dysplasia have been identified in NF1 but the occurrence of meningoceles at the skull base is extremely rare. A rare instance of jugular foramen meningocele being identified in an NF1 patient on imaging is described in this paper. To the best of our knowledge, only two such cases have been reported in the English literature.
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spelling pubmed-57570982018-02-12 Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient Serindere, Mehmet Tasar, Mustafa Hamcan, Salih Bozlar, Ugur Case Rep Radiol Case Report Neurofibromatosis type I (NF1) is a neurocutaneous disorder that involves autosomal dominant transmission. Skull defects, including sphenoid dysplasia and calvarial defects, are a rare finding in patients with NF1. Spinal meningocele and sphenoid wing dysplasia have been identified in NF1 but the occurrence of meningoceles at the skull base is extremely rare. A rare instance of jugular foramen meningocele being identified in an NF1 patient on imaging is described in this paper. To the best of our knowledge, only two such cases have been reported in the English literature. Hindawi 2017 2017-12-24 /pmc/articles/PMC5757098/ /pubmed/29435380 http://dx.doi.org/10.1155/2017/7047696 Text en Copyright © 2017 Mehmet Serindere et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Serindere, Mehmet
Tasar, Mustafa
Hamcan, Salih
Bozlar, Ugur
Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient
title Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient
title_full Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient
title_fullStr Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient
title_full_unstemmed Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient
title_short Imaging Findings of Jugular Foramen Meningocele in a Neurofibromatosis Type 1 Patient
title_sort imaging findings of jugular foramen meningocele in a neurofibromatosis type 1 patient
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757098/
https://www.ncbi.nlm.nih.gov/pubmed/29435380
http://dx.doi.org/10.1155/2017/7047696
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