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Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease

This study analyzed the clinical significance and characteristics of asymmetric venous blood flow in patients with Moyamoya disease (MMD) using minimum intensity projection (minIP) susceptibility-weighted imaging. The minIP views of 30 patients diagnosed with MMD were retrospectively analyzed using...

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Autores principales: Han, Min Jeong, Kim, Sun Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575748/
https://www.ncbi.nlm.nih.gov/pubmed/36254048
http://dx.doi.org/10.1097/MD.0000000000031067
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author Han, Min Jeong
Kim, Sun Jun
author_facet Han, Min Jeong
Kim, Sun Jun
author_sort Han, Min Jeong
collection PubMed
description This study analyzed the clinical significance and characteristics of asymmetric venous blood flow in patients with Moyamoya disease (MMD) using minimum intensity projection (minIP) susceptibility-weighted imaging. The minIP views of 30 patients diagnosed with MMD were retrospectively analyzed using clinical features, brain magnetic resonance angiography, electroencephalography, and brain single-photon emission computed tomography (SPECT). Simultaneously, differences between patients with acute cerebral infarction and non-MMD causes were analyzed. Twelve (40.0%) of the 30 patients had asymmetrical venous flow, which is usually seen in patients with acute cerebral infarction (P = .146). They also had significantly higher Suzuki stages than symmetric patients (P = .014), with five (41.7%) and three (25.0%) of them in stages 4 and 5, respectively. When the Suzuki stages of both hemispheres were different, more veins were found in the stenotic hemisphere (88.9%). Brain SPECT showed more severe hypoperfusion on the side with prominent vascularity in the minIP view (100.0%). Additionally, asymmetric blood flow was observed in 66.7% of the patients with cerebral infarction caused by MMD, whereas only 11.1% of the children with cerebral infarction caused by non-MMD had asymmetry (P = .005). Patients with MMD showed asymmetric hypointensity of the cortical veins with a minIP appearance. The venous structure showed greater signal loss on SWI and was more prominent in the hemisphere where stenosis was advanced or infarction occurred in other examinations. Cerebral infarction in patients with MMD tended to occur with asymmetrically prominent venous patterns with damaged areas in minIP images, which had distinct characteristics from those of patients without MMD.
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spelling pubmed-95757482022-10-17 Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease Han, Min Jeong Kim, Sun Jun Medicine (Baltimore) 5300 This study analyzed the clinical significance and characteristics of asymmetric venous blood flow in patients with Moyamoya disease (MMD) using minimum intensity projection (minIP) susceptibility-weighted imaging. The minIP views of 30 patients diagnosed with MMD were retrospectively analyzed using clinical features, brain magnetic resonance angiography, electroencephalography, and brain single-photon emission computed tomography (SPECT). Simultaneously, differences between patients with acute cerebral infarction and non-MMD causes were analyzed. Twelve (40.0%) of the 30 patients had asymmetrical venous flow, which is usually seen in patients with acute cerebral infarction (P = .146). They also had significantly higher Suzuki stages than symmetric patients (P = .014), with five (41.7%) and three (25.0%) of them in stages 4 and 5, respectively. When the Suzuki stages of both hemispheres were different, more veins were found in the stenotic hemisphere (88.9%). Brain SPECT showed more severe hypoperfusion on the side with prominent vascularity in the minIP view (100.0%). Additionally, asymmetric blood flow was observed in 66.7% of the patients with cerebral infarction caused by MMD, whereas only 11.1% of the children with cerebral infarction caused by non-MMD had asymmetry (P = .005). Patients with MMD showed asymmetric hypointensity of the cortical veins with a minIP appearance. The venous structure showed greater signal loss on SWI and was more prominent in the hemisphere where stenosis was advanced or infarction occurred in other examinations. Cerebral infarction in patients with MMD tended to occur with asymmetrically prominent venous patterns with damaged areas in minIP images, which had distinct characteristics from those of patients without MMD. Lippincott Williams & Wilkins 2022-10-14 /pmc/articles/PMC9575748/ /pubmed/36254048 http://dx.doi.org/10.1097/MD.0000000000031067 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5300
Han, Min Jeong
Kim, Sun Jun
Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
title Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
title_full Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
title_fullStr Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
title_full_unstemmed Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
title_short Clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
title_sort clinical significance of asymmetric venous vasculature on minimum-intensity projection in patients with moyamoya disease
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575748/
https://www.ncbi.nlm.nih.gov/pubmed/36254048
http://dx.doi.org/10.1097/MD.0000000000031067
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