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A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage

Primary intraventricular haemorrhage (PIVH) is rare. Dural arteriovenous fistula causing PIVH is extremely rare. We report a case of a 17 year old boy who presented with left hemiparesis, left lower motor neuron facial palsy and ataxia. His computed tomography head revealed primary intraventricular...

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Autores principales: Srivastava, Trilochan, Sannegowda, Raghavendra Bakki, Sinha, V. D., Jain, R. S., Jain, Rahul, Mathur, Tarun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409390/
https://www.ncbi.nlm.nih.gov/pubmed/28484554
http://dx.doi.org/10.4103/1793-5482.146399
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author Srivastava, Trilochan
Sannegowda, Raghavendra Bakki
Sinha, V. D.
Jain, R. S.
Jain, Rahul
Mathur, Tarun
author_facet Srivastava, Trilochan
Sannegowda, Raghavendra Bakki
Sinha, V. D.
Jain, R. S.
Jain, Rahul
Mathur, Tarun
author_sort Srivastava, Trilochan
collection PubMed
description Primary intraventricular haemorrhage (PIVH) is rare. Dural arteriovenous fistula causing PIVH is extremely rare. We report a case of a 17 year old boy who presented with left hemiparesis, left lower motor neuron facial palsy and ataxia. His computed tomography head revealed primary intraventricular hemorrhage. Catheter super selective angiography revealed a dural arterio venous fistula with arterial feeder arising from the middle meningeal artery as well as from the inferior marginal tentorial artery. Glue injection led to successful disappearance of the fistula and eventual clinical recovery.
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spelling pubmed-54093902017-05-08 A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage Srivastava, Trilochan Sannegowda, Raghavendra Bakki Sinha, V. D. Jain, R. S. Jain, Rahul Mathur, Tarun Asian J Neurosurg Case Report Primary intraventricular haemorrhage (PIVH) is rare. Dural arteriovenous fistula causing PIVH is extremely rare. We report a case of a 17 year old boy who presented with left hemiparesis, left lower motor neuron facial palsy and ataxia. His computed tomography head revealed primary intraventricular hemorrhage. Catheter super selective angiography revealed a dural arterio venous fistula with arterial feeder arising from the middle meningeal artery as well as from the inferior marginal tentorial artery. Glue injection led to successful disappearance of the fistula and eventual clinical recovery. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5409390/ /pubmed/28484554 http://dx.doi.org/10.4103/1793-5482.146399 Text en Copyright: © 2014 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Srivastava, Trilochan
Sannegowda, Raghavendra Bakki
Sinha, V. D.
Jain, R. S.
Jain, Rahul
Mathur, Tarun
A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
title A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
title_full A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
title_fullStr A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
title_full_unstemmed A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
title_short A rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
title_sort rare case of dural arteriovenous fistula presenting as primary intraventricular hemorrhage
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409390/
https://www.ncbi.nlm.nih.gov/pubmed/28484554
http://dx.doi.org/10.4103/1793-5482.146399
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