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...

Full description

Bibliographic Details
Main Authors: J. J. Gold, J. R. Crawford
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Case Reports in Critical Care
Online Access:http://dx.doi.org/10.1155/2013/627972
id doaj-512b799aa02e428e8cb0c59cfd4314f2
record_format Article
spelling 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
work_keys_str_mv AT jjgold anunusualcauseofpediatricstrokesecondarytocongenitalbasilararteryfenestration
AT jrcrawford anunusualcauseofpediatricstrokesecondarytocongenitalbasilararteryfenestration
AT jjgold unusualcauseofpediatricstrokesecondarytocongenitalbasilararteryfenestration
AT jrcrawford unusualcauseofpediatricstrokesecondarytocongenitalbasilararteryfenestration
_version_ 1716798288543350784