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Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()

Neurofibromatosis type 1 is an autosomal dominant genetic disorder with multisystem manifestations including vascular abnormalities. The condition is also associated with an increased risk of both ischemic and hemorrhagic stroke. Here we report a case of a 60-year-old male with known neurofibromatos...

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Autores principales: Desmond, Fiona J., Buture, Alina, Kavanagh, Eoin C., Murphy, Sean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294049/
https://www.ncbi.nlm.nih.gov/pubmed/35865363
http://dx.doi.org/10.1016/j.radcr.2022.05.029
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author Desmond, Fiona J.
Buture, Alina
Kavanagh, Eoin C.
Murphy, Sean
author_facet Desmond, Fiona J.
Buture, Alina
Kavanagh, Eoin C.
Murphy, Sean
author_sort Desmond, Fiona J.
collection PubMed
description Neurofibromatosis type 1 is an autosomal dominant genetic disorder with multisystem manifestations including vascular abnormalities. The condition is also associated with an increased risk of both ischemic and hemorrhagic stroke. Here we report a case of a 60-year-old male with known neurofibromatosis who presented with right sided hemiparesis. Neuroimaging work-up revealed left internal carotid artery dissection and tandem occlusion of the left internal carotid artery and left middle cerebral artery. There was associated territorial ischemic infarction. The patient was found to have extensive intra and extra cranial vasculopathy including gross basilar dolichoectasia and a right-sided cervical internal carotid artery pseudoaneurysm. This case highlights the clinical significance of neurofibromatosis associated vasculopathy which can result in stroke.
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spelling pubmed-92940492022-07-20 Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1() Desmond, Fiona J. Buture, Alina Kavanagh, Eoin C. Murphy, Sean Radiol Case Rep Case Report Neurofibromatosis type 1 is an autosomal dominant genetic disorder with multisystem manifestations including vascular abnormalities. The condition is also associated with an increased risk of both ischemic and hemorrhagic stroke. Here we report a case of a 60-year-old male with known neurofibromatosis who presented with right sided hemiparesis. Neuroimaging work-up revealed left internal carotid artery dissection and tandem occlusion of the left internal carotid artery and left middle cerebral artery. There was associated territorial ischemic infarction. The patient was found to have extensive intra and extra cranial vasculopathy including gross basilar dolichoectasia and a right-sided cervical internal carotid artery pseudoaneurysm. This case highlights the clinical significance of neurofibromatosis associated vasculopathy which can result in stroke. Elsevier 2022-07-16 /pmc/articles/PMC9294049/ /pubmed/35865363 http://dx.doi.org/10.1016/j.radcr.2022.05.029 Text en © 2022 Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Desmond, Fiona J.
Buture, Alina
Kavanagh, Eoin C.
Murphy, Sean
Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
title Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
title_full Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
title_fullStr Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
title_full_unstemmed Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
title_short Ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
title_sort ischemic stroke with extensive vasculopathy in a patient with neurofibromatosis type 1()
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294049/
https://www.ncbi.nlm.nih.gov/pubmed/35865363
http://dx.doi.org/10.1016/j.radcr.2022.05.029
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