An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration
Basilar artery fenestration is an uncommon congenital variant that has been associated with aneurysms and posterior circulation infarcts in the adult literature. Little is known about the functional consequences of basilar artery fenestration, if any, in childhood. We present a case of a previously...
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2013-01-01
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Series: | Case Reports in Critical Care |
Online Access: | http://dx.doi.org/10.1155/2013/627972 |
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doaj-512b799aa02e428e8cb0c59cfd4314f22020-11-24T20:53:02ZengHindawi LimitedCase Reports in Critical Care2090-64202090-64392013-01-01201310.1155/2013/627972627972An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery FenestrationJ. J. Gold0J. R. Crawford1Division of Child Neurology, Department of Neurosciences, Rady Children’s Hospital-San Diego and University of California, 8010 Frost Street Suite 400, San Diego, CA 92123, USADivision of Child Neurology, Department of Neurosciences, Rady Children’s Hospital-San Diego and University of California, 8010 Frost Street Suite 400, San Diego, CA 92123, USABasilar artery fenestration is an uncommon congenital variant that has been associated with aneurysms and posterior circulation infarcts in the adult literature. Little is known about the functional consequences of basilar artery fenestration, if any, in childhood. We present a case of a previously healthy 12-year-old boy who presented with diplopia, tinnitus, and ataxia who had subtle findings on diffusion-weighted magnetic resonance imaging consistent with posterior circulation territory infarction. Computed tomography angiography and magnetic resonance angiography revealed an area of signal abnormality in the basilar artery, which was confirmed on conventional angiography to be a type 2 basilar artery fenestration, without thrombus or aneurysm. The patient recovered from his neurologic deficits over two days and was placed on prophylactic aspirin therapy without recurrence of symptoms. This rare anatomic variant of the posterior circulation is important for physicians to recognize and may have associated neurologic consequences during childhood worthy of further investigation.http://dx.doi.org/10.1155/2013/627972 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
J. J. Gold J. R. Crawford |
spellingShingle |
J. J. Gold J. R. Crawford An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration Case Reports in Critical Care |
author_facet |
J. J. Gold J. R. Crawford |
author_sort |
J. J. Gold |
title |
An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration |
title_short |
An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration |
title_full |
An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration |
title_fullStr |
An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration |
title_full_unstemmed |
An Unusual Cause of Pediatric Stroke Secondary to Congenital Basilar Artery Fenestration |
title_sort |
unusual cause of pediatric stroke secondary to congenital basilar artery fenestration |
publisher |
Hindawi Limited |
series |
Case Reports in Critical Care |
issn |
2090-6420 2090-6439 |
publishDate |
2013-01-01 |
description |
Basilar artery fenestration is an uncommon congenital variant that has been associated with aneurysms and posterior circulation infarcts in the adult literature. Little is known about the functional consequences of basilar artery fenestration, if any, in childhood. We present a case of a previously healthy 12-year-old boy who presented with diplopia, tinnitus, and ataxia who had subtle findings on diffusion-weighted magnetic resonance imaging consistent with posterior circulation territory infarction. Computed tomography angiography and magnetic resonance angiography revealed an area of signal abnormality in the basilar artery, which was confirmed on conventional angiography to be a type 2 basilar artery fenestration, without thrombus or aneurysm. The patient recovered from his neurologic deficits over two days and was placed on prophylactic aspirin therapy without recurrence of symptoms. This rare anatomic variant of the posterior circulation is important for physicians to recognize and may have associated neurologic consequences during childhood worthy of further investigation. |
url |
http://dx.doi.org/10.1155/2013/627972 |
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