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Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report
BACKGROUND: Cerebral arteriovenous malformations (AVMs) are vascular lesions with a network of dysplastic vessels between an arterial and a venous tree with no intervening capillary bed. They most commonly present with an acute hemorrhage, seizures, or persistent headaches. CASE DESCRIPTION: The aut...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Scientific Scholar
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744769/ https://www.ncbi.nlm.nih.gov/pubmed/31528464 http://dx.doi.org/10.25259/SNI-260-2019 |
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author | Saiegh, Fadi Al Hines, Kevin Mouchtouris, Nikolaos Theofanis, Thana Jabbour, Pascal Rosenwasser, Robert Tjoumakaris, Stavropoula |
author_facet | Saiegh, Fadi Al Hines, Kevin Mouchtouris, Nikolaos Theofanis, Thana Jabbour, Pascal Rosenwasser, Robert Tjoumakaris, Stavropoula |
author_sort | Saiegh, Fadi Al |
collection | PubMed |
description | BACKGROUND: Cerebral arteriovenous malformations (AVMs) are vascular lesions with a network of dysplastic vessels between an arterial and a venous tree with no intervening capillary bed. They most commonly present with an acute hemorrhage, seizures, or persistent headaches. CASE DESCRIPTION: The authors report the case of a 62-year-old male who presented with diplopia for 5 days. Magnetic resonance imaging and angiography demonstrated a Spetzler-Martin Grade 2 AVM located in the right frontal operculum with deep drainage into the basal vein of Rosenthal causing ipsilateral oculomotor neuropathy. The patient underwent staged embolizations of the feeding pedicles, which were derived from the internal as well as external carotid circulation. This was followed by a right pterional craniotomy for resection of the AVM. The patient reported complete resolution of the diplopia over 4 weeks with no recurrence at the 6-month follow-up appointment. CONLUSION: AVMs of the brain can present with atypical clinical symptoms that can be caused by the venous drainage pattern not the location. It is important to include vascular imaging studies in the work-up of patients who present with diplopia to rule out an AVM. Early diagnosis and treatment of the AVM can result in complete resolution of the diplopia. |
format | Online Article Text |
id | pubmed-6744769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-67447692019-09-16 Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report Saiegh, Fadi Al Hines, Kevin Mouchtouris, Nikolaos Theofanis, Thana Jabbour, Pascal Rosenwasser, Robert Tjoumakaris, Stavropoula Surg Neurol Int Case Report BACKGROUND: Cerebral arteriovenous malformations (AVMs) are vascular lesions with a network of dysplastic vessels between an arterial and a venous tree with no intervening capillary bed. They most commonly present with an acute hemorrhage, seizures, or persistent headaches. CASE DESCRIPTION: The authors report the case of a 62-year-old male who presented with diplopia for 5 days. Magnetic resonance imaging and angiography demonstrated a Spetzler-Martin Grade 2 AVM located in the right frontal operculum with deep drainage into the basal vein of Rosenthal causing ipsilateral oculomotor neuropathy. The patient underwent staged embolizations of the feeding pedicles, which were derived from the internal as well as external carotid circulation. This was followed by a right pterional craniotomy for resection of the AVM. The patient reported complete resolution of the diplopia over 4 weeks with no recurrence at the 6-month follow-up appointment. CONLUSION: AVMs of the brain can present with atypical clinical symptoms that can be caused by the venous drainage pattern not the location. It is important to include vascular imaging studies in the work-up of patients who present with diplopia to rule out an AVM. Early diagnosis and treatment of the AVM can result in complete resolution of the diplopia. Scientific Scholar 2019-06-28 /pmc/articles/PMC6744769/ /pubmed/31528464 http://dx.doi.org/10.25259/SNI-260-2019 Text en Copyright: © 2019 Surgical Neurology International http://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 | Case Report Saiegh, Fadi Al Hines, Kevin Mouchtouris, Nikolaos Theofanis, Thana Jabbour, Pascal Rosenwasser, Robert Tjoumakaris, Stavropoula Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report |
title | Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report |
title_full | Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report |
title_fullStr | Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report |
title_full_unstemmed | Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report |
title_short | Oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: A case report |
title_sort | oculomotor neuropathy from an unruptured arteriovenous malformation in the frontal operculum: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6744769/ https://www.ncbi.nlm.nih.gov/pubmed/31528464 http://dx.doi.org/10.25259/SNI-260-2019 |
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