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A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus

OBJECTIVE: The falx cerebri is known to have venous plexuses. Although some cases of dural arteriovenous fistula (DAVF) associated with falcine sinus have been reported, DAVF in the falx with prominent falcine venous plexus has not previously been reported. CASE PRESENTATION: A 59-year-old male was...

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Autores principales: Satoh, Daisuke, Sasaki, Tetsuo, Yako, Takehiro, Kitazawa, Kazuo, Kobayashi, Shigeaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Neuroendovascular Therapy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370889/
https://www.ncbi.nlm.nih.gov/pubmed/37502783
http://dx.doi.org/10.5797/jnet.cr.2020-0142
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author Satoh, Daisuke
Sasaki, Tetsuo
Yako, Takehiro
Kitazawa, Kazuo
Kobayashi, Shigeaki
author_facet Satoh, Daisuke
Sasaki, Tetsuo
Yako, Takehiro
Kitazawa, Kazuo
Kobayashi, Shigeaki
author_sort Satoh, Daisuke
collection PubMed
description OBJECTIVE: The falx cerebri is known to have venous plexuses. Although some cases of dural arteriovenous fistula (DAVF) associated with falcine sinus have been reported, DAVF in the falx with prominent falcine venous plexus has not previously been reported. CASE PRESENTATION: A 59-year-old male was hospitalized with head trauma. MRI incidentally showed a possible occipital DAVF. CTA and DSA revealed a DAVF in the flax with prominent falcine venous plexus. We performed a selective transarterial embolization with glue and particle, obtaining a complete occlusion of the fistula. CONCLUSION: We report a rare case of DAVF in the flax with prominent falcine venous plexus that was successfully treated by a transarterial embolization.
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spelling pubmed-103708892023-07-27 A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus Satoh, Daisuke Sasaki, Tetsuo Yako, Takehiro Kitazawa, Kazuo Kobayashi, Shigeaki J Neuroendovasc Ther Case Report OBJECTIVE: The falx cerebri is known to have venous plexuses. Although some cases of dural arteriovenous fistula (DAVF) associated with falcine sinus have been reported, DAVF in the falx with prominent falcine venous plexus has not previously been reported. CASE PRESENTATION: A 59-year-old male was hospitalized with head trauma. MRI incidentally showed a possible occipital DAVF. CTA and DSA revealed a DAVF in the flax with prominent falcine venous plexus. We performed a selective transarterial embolization with glue and particle, obtaining a complete occlusion of the fistula. CONCLUSION: We report a rare case of DAVF in the flax with prominent falcine venous plexus that was successfully treated by a transarterial embolization. The Japanese Society for Neuroendovascular Therapy 2020-12-29 2021 /pmc/articles/PMC10370889/ /pubmed/37502783 http://dx.doi.org/10.5797/jnet.cr.2020-0142 Text en ©2021 The Japanese Society for Neuroendovascular Therapy https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives International License (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Case Report
Satoh, Daisuke
Sasaki, Tetsuo
Yako, Takehiro
Kitazawa, Kazuo
Kobayashi, Shigeaki
A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus
title A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus
title_full A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus
title_fullStr A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus
title_full_unstemmed A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus
title_short A Case of Dural Arteriovenous Fistula in the Falx with Prominent Falcine Venous Plexus
title_sort case of dural arteriovenous fistula in the falx with prominent falcine venous plexus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370889/
https://www.ncbi.nlm.nih.gov/pubmed/37502783
http://dx.doi.org/10.5797/jnet.cr.2020-0142
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