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An unusual case of pediatric bow hunter's stroke
BACKGROUND: Bow Hunter's syndrome/stroke is defined as symptomatic, vertebrobasilar insufficiency provoked by physiologic head rotation. It is a diagnostically challenging cause of posterior circulation stroke in children. While there have been prior reports of this rare disorder, we describe a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841921/ https://www.ncbi.nlm.nih.gov/pubmed/24340230 http://dx.doi.org/10.4103/2152-7806.121647 |
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author | Anene-Maidoh, Tony I. Vega, Rafael A. Fautheree, Gregory L. Reavey-Cantwell, John F. |
author_facet | Anene-Maidoh, Tony I. Vega, Rafael A. Fautheree, Gregory L. Reavey-Cantwell, John F. |
author_sort | Anene-Maidoh, Tony I. |
collection | PubMed |
description | BACKGROUND: Bow Hunter's syndrome/stroke is defined as symptomatic, vertebrobasilar insufficiency provoked by physiologic head rotation. It is a diagnostically challenging cause of posterior circulation stroke in children. While there have been prior reports of this rare disorder, we describe an exceptional case of pediatric Bow Hunter's stroke resulting from a near complete occlusion the right vertebral artery (VA) secondary to an anomalous spur emanating from the right occipital condyle. Surgical and endovascular options and approaches are also detailed herein. CASE DESCRIPTION: A 16-year-old male presented with multiple posterior circulation ischemic strokes. A dynamic computerized tomography angiogram performed with the patient's head in a rotated position revealed a near complete occlusion of the V3 segment of the right VA from a bone spur arising from his occipital condyle. The spur caused a focal dissection of the distal right VA with associated thrombus. He was initially managed with a cervical collar, antiplatelet therapy with aspirin 81 mg and anticoagulation with coumadin (INR goal 2-3) for 3 months. Despite the management plan, he had a subsequent thromboembolic event and a right VA sacrifice with coil embolization was then performed. At the 3-month follow-up, the patient was doing well with no reports of any subsequent strokes. CONCLUSION: We report the first reported pediatric case of Bow Hunter's stroke due to dynamic right VA occlusion from an occipital condylar bone spur. The vascular compression from this spur led to a right VA dissection and thrombus formation and ultimately caused multiple posterior circulation thromboembolic strokes. Endovascular treatment options including vessel sacrifice should be considered in cases that have failed maximal medical management. |
format | Online Article Text |
id | pubmed-3841921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38419212013-12-11 An unusual case of pediatric bow hunter's stroke Anene-Maidoh, Tony I. Vega, Rafael A. Fautheree, Gregory L. Reavey-Cantwell, John F. Surg Neurol Int Case Report BACKGROUND: Bow Hunter's syndrome/stroke is defined as symptomatic, vertebrobasilar insufficiency provoked by physiologic head rotation. It is a diagnostically challenging cause of posterior circulation stroke in children. While there have been prior reports of this rare disorder, we describe an exceptional case of pediatric Bow Hunter's stroke resulting from a near complete occlusion the right vertebral artery (VA) secondary to an anomalous spur emanating from the right occipital condyle. Surgical and endovascular options and approaches are also detailed herein. CASE DESCRIPTION: A 16-year-old male presented with multiple posterior circulation ischemic strokes. A dynamic computerized tomography angiogram performed with the patient's head in a rotated position revealed a near complete occlusion of the V3 segment of the right VA from a bone spur arising from his occipital condyle. The spur caused a focal dissection of the distal right VA with associated thrombus. He was initially managed with a cervical collar, antiplatelet therapy with aspirin 81 mg and anticoagulation with coumadin (INR goal 2-3) for 3 months. Despite the management plan, he had a subsequent thromboembolic event and a right VA sacrifice with coil embolization was then performed. At the 3-month follow-up, the patient was doing well with no reports of any subsequent strokes. CONCLUSION: We report the first reported pediatric case of Bow Hunter's stroke due to dynamic right VA occlusion from an occipital condylar bone spur. The vascular compression from this spur led to a right VA dissection and thrombus formation and ultimately caused multiple posterior circulation thromboembolic strokes. Endovascular treatment options including vessel sacrifice should be considered in cases that have failed maximal medical management. Medknow Publications & Media Pvt Ltd 2013-11-20 /pmc/articles/PMC3841921/ /pubmed/24340230 http://dx.doi.org/10.4103/2152-7806.121647 Text en Copyright: © 2013 Anene-Maidoh TI. 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 Anene-Maidoh, Tony I. Vega, Rafael A. Fautheree, Gregory L. Reavey-Cantwell, John F. An unusual case of pediatric bow hunter's stroke |
title | An unusual case of pediatric bow hunter's stroke |
title_full | An unusual case of pediatric bow hunter's stroke |
title_fullStr | An unusual case of pediatric bow hunter's stroke |
title_full_unstemmed | An unusual case of pediatric bow hunter's stroke |
title_short | An unusual case of pediatric bow hunter's stroke |
title_sort | unusual case of pediatric bow hunter's stroke |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841921/ https://www.ncbi.nlm.nih.gov/pubmed/24340230 http://dx.doi.org/10.4103/2152-7806.121647 |
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