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Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease

BACKGROUND: The incidence of symptomatic hyperperfusion syndrome after superficial temporal artery-middle cerebral artery (STA-MCA) anastomosis for patients with moyamoya disease (MMD) approaches 30%. In most cases, hyperperfusion occurs in a localized area and disappears within 1-2 weeks. CASE DESC...

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Autores principales: Takemoto, Yushin, Morioka, Motohiro, Nakagawa, Takashi, Hasegawa, Yu, Ohmori, Yuki, Kawano, Takayuki, Kai, Yutaka, Kuratsu, Jun-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475882/
https://www.ncbi.nlm.nih.gov/pubmed/23087822
http://dx.doi.org/10.4103/2152-7806.100867
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author Takemoto, Yushin
Morioka, Motohiro
Nakagawa, Takashi
Hasegawa, Yu
Ohmori, Yuki
Kawano, Takayuki
Kai, Yutaka
Kuratsu, Jun-ichi
author_facet Takemoto, Yushin
Morioka, Motohiro
Nakagawa, Takashi
Hasegawa, Yu
Ohmori, Yuki
Kawano, Takayuki
Kai, Yutaka
Kuratsu, Jun-ichi
author_sort Takemoto, Yushin
collection PubMed
description BACKGROUND: The incidence of symptomatic hyperperfusion syndrome after superficial temporal artery-middle cerebral artery (STA-MCA) anastomosis for patients with moyamoya disease (MMD) approaches 30%. In most cases, hyperperfusion occurs in a localized area and disappears within 1-2 weeks. CASE DESCRIPTION: A 59-year-old female diagnosed with asymptomatic MMD for 4 months became rapidly symptomatic with transient ischemic attacks (TIAs). After left STA-MCA anastomosis surgery, she developed symptomatic hyperperfusion, initially (1-2 weeks after surgery) manifesting with severe headache and lesions located in the left basal ganglia. She then developed (2-5 weeks after surgery) aphasia and right hemiparesis caused by new hyperperfusion lesions located in the left frontal area. At discharge (7 weeks after surgery), she recovered fully without any remaining neurologic deficit and no ischemic lesions. CONCLUSION: This report details a rare case of a patient with MMD who presented with regionally progressive hyperperfusion lesions after STA-MCA anastomosis and symptoms that persisted for 5 weeks following surgery. Results from this case suggest that regional differences exist in the functional recovery of cerebrovascular reactivity (CVR) in a patient with rapidly progressive MMD.
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spelling pubmed-34758822012-10-19 Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease Takemoto, Yushin Morioka, Motohiro Nakagawa, Takashi Hasegawa, Yu Ohmori, Yuki Kawano, Takayuki Kai, Yutaka Kuratsu, Jun-ichi Surg Neurol Int Case Report BACKGROUND: The incidence of symptomatic hyperperfusion syndrome after superficial temporal artery-middle cerebral artery (STA-MCA) anastomosis for patients with moyamoya disease (MMD) approaches 30%. In most cases, hyperperfusion occurs in a localized area and disappears within 1-2 weeks. CASE DESCRIPTION: A 59-year-old female diagnosed with asymptomatic MMD for 4 months became rapidly symptomatic with transient ischemic attacks (TIAs). After left STA-MCA anastomosis surgery, she developed symptomatic hyperperfusion, initially (1-2 weeks after surgery) manifesting with severe headache and lesions located in the left basal ganglia. She then developed (2-5 weeks after surgery) aphasia and right hemiparesis caused by new hyperperfusion lesions located in the left frontal area. At discharge (7 weeks after surgery), she recovered fully without any remaining neurologic deficit and no ischemic lesions. CONCLUSION: This report details a rare case of a patient with MMD who presented with regionally progressive hyperperfusion lesions after STA-MCA anastomosis and symptoms that persisted for 5 weeks following surgery. Results from this case suggest that regional differences exist in the functional recovery of cerebrovascular reactivity (CVR) in a patient with rapidly progressive MMD. Medknow Publications & Media Pvt Ltd 2012-09-13 /pmc/articles/PMC3475882/ /pubmed/23087822 http://dx.doi.org/10.4103/2152-7806.100867 Text en Copyright: © 2012 Takemoto Y. 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
Takemoto, Yushin
Morioka, Motohiro
Nakagawa, Takashi
Hasegawa, Yu
Ohmori, Yuki
Kawano, Takayuki
Kai, Yutaka
Kuratsu, Jun-ichi
Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
title Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
title_full Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
title_fullStr Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
title_full_unstemmed Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
title_short Prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
title_sort prolonged and regionally progressive symptomatic cerebral hyperperfusion syndrome after superficial temporal artery-middle cerebral artery anastomosis in a patient with moyamoya disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475882/
https://www.ncbi.nlm.nih.gov/pubmed/23087822
http://dx.doi.org/10.4103/2152-7806.100867
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