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Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization
BACKGROUND: Intracranial giant vertebral artery aneurysms are extremely rare in the pediatric population and are associated with significant morbidity and mortality. The present report describes a case of a pediatric patient with giant vertebral artery aneurysm who presented with intracranial mass e...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109167/ https://www.ncbi.nlm.nih.gov/pubmed/25071937 http://dx.doi.org/10.4103/2152-7806.134807 |
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author | Park, Hun-Soo Nakagawa, Ichiro Wada, Takeshi Nakagawa, Hiroyuki Hironaka, Yasuo Kichikawa, Kimihiko Nakase, Hiroyuki |
author_facet | Park, Hun-Soo Nakagawa, Ichiro Wada, Takeshi Nakagawa, Hiroyuki Hironaka, Yasuo Kichikawa, Kimihiko Nakase, Hiroyuki |
author_sort | Park, Hun-Soo |
collection | PubMed |
description | BACKGROUND: Intracranial giant vertebral artery aneurysms are extremely rare in the pediatric population and are associated with significant morbidity and mortality. The present report describes a case of a pediatric patient with giant vertebral artery aneurysm who presented with intracranial mass effect. This patient was successfully treated with endovascular parent artery occlusion and coil embolization. CASE DESCRIPTION: A 7-year-old girl presented with tetraparesis, ataxia, dysphagia, and dysphonia. Cerebral angiography revealed intracranial giant aneurysm arising from the right vertebral artery. The patient underwent endovascular parent artery occlusion alone to facilitate aneurysmal thrombosis as an initial treatment. This was done to avoid a coil mass effect to the brainstem. However, incomplete thrombosis occurred in the vicinity of the vertebral artery union. Therefore, additional coil embolization for residual aneurysm was performed. Two additional coil embolization procedures were performed in response to recurrence. Mass effect and clinical symptoms gradually improved, and the patient had no associated morbidity or recurrence at 2 years after the last fourth coil embolization. CONCLUSION: Intracranial giant vertebral artery aneurysms are rare and challenging in pediatric patients. Staged endovascular strategy can be a safe and effective treatment option. |
format | Online Article Text |
id | pubmed-4109167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41091672014-07-28 Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization Park, Hun-Soo Nakagawa, Ichiro Wada, Takeshi Nakagawa, Hiroyuki Hironaka, Yasuo Kichikawa, Kimihiko Nakase, Hiroyuki Surg Neurol Int Surgical Neurology International: Unique Case Observations BACKGROUND: Intracranial giant vertebral artery aneurysms are extremely rare in the pediatric population and are associated with significant morbidity and mortality. The present report describes a case of a pediatric patient with giant vertebral artery aneurysm who presented with intracranial mass effect. This patient was successfully treated with endovascular parent artery occlusion and coil embolization. CASE DESCRIPTION: A 7-year-old girl presented with tetraparesis, ataxia, dysphagia, and dysphonia. Cerebral angiography revealed intracranial giant aneurysm arising from the right vertebral artery. The patient underwent endovascular parent artery occlusion alone to facilitate aneurysmal thrombosis as an initial treatment. This was done to avoid a coil mass effect to the brainstem. However, incomplete thrombosis occurred in the vicinity of the vertebral artery union. Therefore, additional coil embolization for residual aneurysm was performed. Two additional coil embolization procedures were performed in response to recurrence. Mass effect and clinical symptoms gradually improved, and the patient had no associated morbidity or recurrence at 2 years after the last fourth coil embolization. CONCLUSION: Intracranial giant vertebral artery aneurysms are rare and challenging in pediatric patients. Staged endovascular strategy can be a safe and effective treatment option. Medknow Publications & Media Pvt Ltd 2014-06-19 /pmc/articles/PMC4109167/ /pubmed/25071937 http://dx.doi.org/10.4103/2152-7806.134807 Text en Copyright: © 2014 Park H 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 | Surgical Neurology International: Unique Case Observations Park, Hun-Soo Nakagawa, Ichiro Wada, Takeshi Nakagawa, Hiroyuki Hironaka, Yasuo Kichikawa, Kimihiko Nakase, Hiroyuki Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
title | Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
title_full | Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
title_fullStr | Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
title_full_unstemmed | Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
title_short | Giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
title_sort | giant vertebral artery aneurysm in a child treated with endovascular parent artery occlusion and coil embolization |
topic | Surgical Neurology International: Unique Case Observations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109167/ https://www.ncbi.nlm.nih.gov/pubmed/25071937 http://dx.doi.org/10.4103/2152-7806.134807 |
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