Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Saiegh, Fadi Al, Hines, Kevin, Mouchtouris, Nikolaos, Theofanis, Thana, Jabbour, Pascal, Rosenwasser, Robert, Tjoumakaris, Stavropoula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Scientific Scholar 2019
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
_version_ 1783451442985566208
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
work_keys_str_mv AT saieghfadial oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport
AT hineskevin oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport
AT mouchtourisnikolaos oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport
AT theofanisthana oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport
AT jabbourpascal oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport
AT rosenwasserrobert oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport
AT tjoumakarisstavropoula oculomotorneuropathyfromanunrupturedarteriovenousmalformationinthefrontaloperculumacasereport