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Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome

BACKGROUND: This study investigated hyperintense vessel signs (HVS) on fluid-attenuated inversion recovery imaging in the P1–2 portions of posterior cerebral arteries (PCAs) as a “hyperintense PCA sign” and HVS of cortical arteries. We retrospectively examined whether these signs would be useful in...

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Autores principales: Imai, Masaaki, Shimoda, Masami, Oda, Shinri, Hoshikawa, Kaori, Osada, Takahiro, Aoki, Rie, Sunaga, Azusa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645486/
https://www.ncbi.nlm.nih.gov/pubmed/34877044
http://dx.doi.org/10.25259/SNI_1023_2021
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author Imai, Masaaki
Shimoda, Masami
Oda, Shinri
Hoshikawa, Kaori
Osada, Takahiro
Aoki, Rie
Sunaga, Azusa
author_facet Imai, Masaaki
Shimoda, Masami
Oda, Shinri
Hoshikawa, Kaori
Osada, Takahiro
Aoki, Rie
Sunaga, Azusa
author_sort Imai, Masaaki
collection PubMed
description BACKGROUND: This study investigated hyperintense vessel signs (HVS) on fluid-attenuated inversion recovery imaging in the P1–2 portions of posterior cerebral arteries (PCAs) as a “hyperintense PCA sign” and HVS of cortical arteries. We retrospectively examined whether these signs would be useful in diagnosing reversible cerebral vasoconstriction syndrome (RCVS) in the acute phase. METHODS: Eighty patients with RCVS who underwent initial magnetic resonance imaging (MRI) within 7 days of onset were included in this study. HVS and related clinical factors were examined. RESULTS: On initial MRI of RCVS patients, hyperintense PCA sign and HVS of cortical arteries were seen in 21 cases (26%) and 38 cases (48%), respectively. In patients showing hyperintense PCA sign, vasoconstriction of the A2–3 portion was a significant clinical factor. Conversely, vasoconstriction of the M1 and P1 portions and the presence of white matter hyperintensity on initial and chronic-stage MRI were significantly associated with the presence of HVS in cortical arteries. CONCLUSION: Because rich collateral flow exists around PCAs, the frequency of hyperintense PCA sign is not high. However, hyperintense PCA sign findings in patients with suspected RCVS offer credible evidence of extreme flow decreases due to vasoconstriction in peripheral PCAs and other arteries associated with the collateral circulation of PCAs. Conversely, HVS in cortical arteries tend to reflect slow antegrade circulation due to vasoconstriction of peripheral vessel and major trunks. Both signs appear useful for auxiliary diagnosis of acute-phase RCVS.
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spelling pubmed-86454862021-12-06 Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome Imai, Masaaki Shimoda, Masami Oda, Shinri Hoshikawa, Kaori Osada, Takahiro Aoki, Rie Sunaga, Azusa Surg Neurol Int Original Article BACKGROUND: This study investigated hyperintense vessel signs (HVS) on fluid-attenuated inversion recovery imaging in the P1–2 portions of posterior cerebral arteries (PCAs) as a “hyperintense PCA sign” and HVS of cortical arteries. We retrospectively examined whether these signs would be useful in diagnosing reversible cerebral vasoconstriction syndrome (RCVS) in the acute phase. METHODS: Eighty patients with RCVS who underwent initial magnetic resonance imaging (MRI) within 7 days of onset were included in this study. HVS and related clinical factors were examined. RESULTS: On initial MRI of RCVS patients, hyperintense PCA sign and HVS of cortical arteries were seen in 21 cases (26%) and 38 cases (48%), respectively. In patients showing hyperintense PCA sign, vasoconstriction of the A2–3 portion was a significant clinical factor. Conversely, vasoconstriction of the M1 and P1 portions and the presence of white matter hyperintensity on initial and chronic-stage MRI were significantly associated with the presence of HVS in cortical arteries. CONCLUSION: Because rich collateral flow exists around PCAs, the frequency of hyperintense PCA sign is not high. However, hyperintense PCA sign findings in patients with suspected RCVS offer credible evidence of extreme flow decreases due to vasoconstriction in peripheral PCAs and other arteries associated with the collateral circulation of PCAs. Conversely, HVS in cortical arteries tend to reflect slow antegrade circulation due to vasoconstriction of peripheral vessel and major trunks. Both signs appear useful for auxiliary diagnosis of acute-phase RCVS. Scientific Scholar 2021-11-16 /pmc/articles/PMC8645486/ /pubmed/34877044 http://dx.doi.org/10.25259/SNI_1023_2021 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Imai, Masaaki
Shimoda, Masami
Oda, Shinri
Hoshikawa, Kaori
Osada, Takahiro
Aoki, Rie
Sunaga, Azusa
Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
title Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
title_full Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
title_fullStr Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
title_full_unstemmed Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
title_short Hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
title_sort hyperintense posterior cerebral artery sign in patients with reversible cerebral vasoconstriction syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645486/
https://www.ncbi.nlm.nih.gov/pubmed/34877044
http://dx.doi.org/10.25259/SNI_1023_2021
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