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A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization
OBJECTIVE: We report a case of anterior cranial fossa dural arteriovenous fistula (dAVF) in which ocular movement was impaired after Onyx embolization from the ophthalmic artery (OphA). CASE PRESENTATION: A 76-year-old male was admitted to our hospital for treatment of an incidentally found anterior...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Japanese Society for Neuroendovascular Therapy
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370653/ https://www.ncbi.nlm.nih.gov/pubmed/37501699 http://dx.doi.org/10.5797/jnet.cr.2019-0021 |
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author | Tanaka, Yuko Yoshiyama, Tomomi Nishiyama, Akira Umesaki, Arisa Nakajou, Takato Matsumoto, Hiroaki Terada, Tomoaki |
author_facet | Tanaka, Yuko Yoshiyama, Tomomi Nishiyama, Akira Umesaki, Arisa Nakajou, Takato Matsumoto, Hiroaki Terada, Tomoaki |
author_sort | Tanaka, Yuko |
collection | PubMed |
description | OBJECTIVE: We report a case of anterior cranial fossa dural arteriovenous fistula (dAVF) in which ocular movement was impaired after Onyx embolization from the ophthalmic artery (OphA). CASE PRESENTATION: A 76-year-old male was admitted to our hospital for treatment of an incidentally found anterior cranial fossa dAVF. Onyx was injected from the right anterior ethmoidal artery (AEA) to close the shunt. Onyx refluxed to the third portion of the OphA to make a plug, but was unable to reach the venous side beyond the shunt; therefore, a small shunt remained. Although his visual acuity and field were normal, vertical diplopia developed after embolization and disappeared 1 month later. Diplopia worsened when the patient tilted his head to the right. Neuro-ophthalmological examination confirmed right superior oblique muscle impairment. The cause of diplopia was considered to be ischemic injury of the superior oblique muscle associated with embolization of the AEA, which provides nutrients to the superior oblique muscle and trochlear nerve. CONCLUSION: Embolization from the OphA beyond the third portion may cause external ophthalmoplegia, although it may heal spontaneously. |
format | Online Article Text |
id | pubmed-10370653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Japanese Society for Neuroendovascular Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-103706532023-07-27 A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization Tanaka, Yuko Yoshiyama, Tomomi Nishiyama, Akira Umesaki, Arisa Nakajou, Takato Matsumoto, Hiroaki Terada, Tomoaki J Neuroendovasc Ther Case Report OBJECTIVE: We report a case of anterior cranial fossa dural arteriovenous fistula (dAVF) in which ocular movement was impaired after Onyx embolization from the ophthalmic artery (OphA). CASE PRESENTATION: A 76-year-old male was admitted to our hospital for treatment of an incidentally found anterior cranial fossa dAVF. Onyx was injected from the right anterior ethmoidal artery (AEA) to close the shunt. Onyx refluxed to the third portion of the OphA to make a plug, but was unable to reach the venous side beyond the shunt; therefore, a small shunt remained. Although his visual acuity and field were normal, vertical diplopia developed after embolization and disappeared 1 month later. Diplopia worsened when the patient tilted his head to the right. Neuro-ophthalmological examination confirmed right superior oblique muscle impairment. The cause of diplopia was considered to be ischemic injury of the superior oblique muscle associated with embolization of the AEA, which provides nutrients to the superior oblique muscle and trochlear nerve. CONCLUSION: Embolization from the OphA beyond the third portion may cause external ophthalmoplegia, although it may heal spontaneously. The Japanese Society for Neuroendovascular Therapy 2020-04-08 2020 /pmc/articles/PMC10370653/ /pubmed/37501699 http://dx.doi.org/10.5797/jnet.cr.2019-0021 Text en ©2020 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 Tanaka, Yuko Yoshiyama, Tomomi Nishiyama, Akira Umesaki, Arisa Nakajou, Takato Matsumoto, Hiroaki Terada, Tomoaki A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization |
title | A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization |
title_full | A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization |
title_fullStr | A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization |
title_full_unstemmed | A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization |
title_short | A Case of Anterior Cranial Fossa Dural Arteriovenous Fistula with Transient Ocular Movement Disorder after Embolization |
title_sort | case of anterior cranial fossa dural arteriovenous fistula with transient ocular movement disorder after embolization |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370653/ https://www.ncbi.nlm.nih.gov/pubmed/37501699 http://dx.doi.org/10.5797/jnet.cr.2019-0021 |
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