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Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature

BACKGROUND: Cerebral arteriovenous malformations (AVMs) have been long thought to be a congenital anomaly of vasculogenesis in which arteries and veins form direct connections forming a vascular nidus without an intervening capillary bed or neural tissue. Scattered case reports have described that A...

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Autores principales: Neil, Jayson A., Li, Daphne, Stiefel, Michael F., Hu, Yin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209707/
https://www.ncbi.nlm.nih.gov/pubmed/25371848
http://dx.doi.org/10.4103/2152-7806.142796
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author Neil, Jayson A.
Li, Daphne
Stiefel, Michael F.
Hu, Yin C.
author_facet Neil, Jayson A.
Li, Daphne
Stiefel, Michael F.
Hu, Yin C.
author_sort Neil, Jayson A.
collection PubMed
description BACKGROUND: Cerebral arteriovenous malformations (AVMs) have been long thought to be a congenital anomaly of vasculogenesis in which arteries and veins form direct connections forming a vascular nidus without an intervening capillary bed or neural tissue. Scattered case reports have described that AVMs may form de novo suggesting they can become an acquired lesion. CASE DESCRIPTION: The current case report describes a patient who presented with new-onset seizures with an initial negative magnetic resonance imaging (MRI) of the brain and subsequently developed an AVM on a MRI 9 years later. CONCLUSION: This case joins a small, but growing body of literature that challenges the notion that all AVMs are congenital.
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spelling pubmed-42097072014-11-04 Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature Neil, Jayson A. Li, Daphne Stiefel, Michael F. Hu, Yin C. Surg Neurol Int Case Report BACKGROUND: Cerebral arteriovenous malformations (AVMs) have been long thought to be a congenital anomaly of vasculogenesis in which arteries and veins form direct connections forming a vascular nidus without an intervening capillary bed or neural tissue. Scattered case reports have described that AVMs may form de novo suggesting they can become an acquired lesion. CASE DESCRIPTION: The current case report describes a patient who presented with new-onset seizures with an initial negative magnetic resonance imaging (MRI) of the brain and subsequently developed an AVM on a MRI 9 years later. CONCLUSION: This case joins a small, but growing body of literature that challenges the notion that all AVMs are congenital. Medknow Publications & Media Pvt Ltd 2014-10-13 /pmc/articles/PMC4209707/ /pubmed/25371848 http://dx.doi.org/10.4103/2152-7806.142796 Text en Copyright: © 2014 Neil JA. http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Case Report
Neil, Jayson A.
Li, Daphne
Stiefel, Michael F.
Hu, Yin C.
Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature
title Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature
title_full Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature
title_fullStr Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature
title_full_unstemmed Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature
title_short Symptomatic de novo arteriovenous malformation in an adult: Case report and review of the literature
title_sort symptomatic de novo arteriovenous malformation in an adult: case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209707/
https://www.ncbi.nlm.nih.gov/pubmed/25371848
http://dx.doi.org/10.4103/2152-7806.142796
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