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Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis

The authors present a rare case of moyamoya disease emerged with corpus callosum hemorrhage. A 31-year-old woman suddenly complained of severe headache followed by consciousness disturbance. Radiological examinations revealed the bleeding in the splenium of corpus callosum, which was associated with...

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Autores principales: Yamamoto, Shusuke, Akioka, Naoki, Kashiwazaki, Daina, Tomita, Takahiro, Kuwayama, Naoya, Kuroda, Satoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Neurosurgical Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386173/
https://www.ncbi.nlm.nih.gov/pubmed/28664005
http://dx.doi.org/10.2176/nmccrj.cr.2016-0010
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author Yamamoto, Shusuke
Akioka, Naoki
Kashiwazaki, Daina
Tomita, Takahiro
Kuwayama, Naoya
Kuroda, Satoshi
author_facet Yamamoto, Shusuke
Akioka, Naoki
Kashiwazaki, Daina
Tomita, Takahiro
Kuwayama, Naoya
Kuroda, Satoshi
author_sort Yamamoto, Shusuke
collection PubMed
description The authors present a rare case of moyamoya disease emerged with corpus callosum hemorrhage. A 31-year-old woman suddenly complained of severe headache followed by consciousness disturbance. Radiological examinations revealed the bleeding in the splenium of corpus callosum, which was associated with intraventricular hemorrhage. On cerebral angiography, the carotid fork was severely stenotic on both sides, and a marked dilatation was observed in the anterior/posterior choroidal arteries and posterior pericallosal artery as well as the lenticulostriate arteries. Therefore, she was diagnosed as moyamoya disease. She successfully underwent superficial temporal artery to middle cerebral artery (STA–MCA) anastomosis and indirect bypass on both sides. Postoperative course was uneventful. Follow-up cerebral angiography performed 4 months after surgery showed well-developed surgical collaterals via the external carotid system and a marked decrease of the dilated moyamoya vessels. She has been free from any cerebrovascular events for 36 months after surgery. Radiological findings strongly suggest that splenial bleeding occurred due to the rupture of the dilated abnormal collateral vessels that originate from the medial posterior choroidal artery and penetrate the corpus callosum in this case. Three-dimensional computer graphic analysis was useful to determine the complex collateral circulation in moyamoya disease.
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spelling pubmed-53861732017-06-29 Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis Yamamoto, Shusuke Akioka, Naoki Kashiwazaki, Daina Tomita, Takahiro Kuwayama, Naoya Kuroda, Satoshi NMC Case Rep J Case Report The authors present a rare case of moyamoya disease emerged with corpus callosum hemorrhage. A 31-year-old woman suddenly complained of severe headache followed by consciousness disturbance. Radiological examinations revealed the bleeding in the splenium of corpus callosum, which was associated with intraventricular hemorrhage. On cerebral angiography, the carotid fork was severely stenotic on both sides, and a marked dilatation was observed in the anterior/posterior choroidal arteries and posterior pericallosal artery as well as the lenticulostriate arteries. Therefore, she was diagnosed as moyamoya disease. She successfully underwent superficial temporal artery to middle cerebral artery (STA–MCA) anastomosis and indirect bypass on both sides. Postoperative course was uneventful. Follow-up cerebral angiography performed 4 months after surgery showed well-developed surgical collaterals via the external carotid system and a marked decrease of the dilated moyamoya vessels. She has been free from any cerebrovascular events for 36 months after surgery. Radiological findings strongly suggest that splenial bleeding occurred due to the rupture of the dilated abnormal collateral vessels that originate from the medial posterior choroidal artery and penetrate the corpus callosum in this case. Three-dimensional computer graphic analysis was useful to determine the complex collateral circulation in moyamoya disease. The Japan Neurosurgical Society 2016-05-16 /pmc/articles/PMC5386173/ /pubmed/28664005 http://dx.doi.org/10.2176/nmccrj.cr.2016-0010 Text en Copyright © 2016 The Japan Neurosurgical Society This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Case Report
Yamamoto, Shusuke
Akioka, Naoki
Kashiwazaki, Daina
Tomita, Takahiro
Kuwayama, Naoya
Kuroda, Satoshi
Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis
title Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis
title_full Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis
title_fullStr Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis
title_full_unstemmed Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis
title_short Moyamoya Disease Emerged with Corpus Callosum Hemorrhage: A 3D Computer Graphic Analysis
title_sort moyamoya disease emerged with corpus callosum hemorrhage: a 3d computer graphic analysis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386173/
https://www.ncbi.nlm.nih.gov/pubmed/28664005
http://dx.doi.org/10.2176/nmccrj.cr.2016-0010
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