Thoracolumbar Glomus-type Intramedullary Arteriovenous Malformations Presenting with Nonperimesencephalic Subarachnoid Hemorrhage: A Case Report

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dc.contributor.authorBüyükkaya, Ramazan
dc.contributor.authorCebeci, Hakan
dc.contributor.authorAydın, Ömer
dc.contributor.authorErdoğan, Cüneyt
dc.contributor.authorHakyemez, Bahattin
dc.date.accessioned2020-04-30T13:33:53Z
dc.date.available2020-04-30T13:33:53Z
dc.date.issued2015
dc.departmentDÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.description.abstractA 22-year-old man presented with severe head and neck pain, nausea, and vomitting at the emergency department. Computed tomography revealed nonperimesencephalic subarachnoid hemorrhage. Subarachnoid hemorrhage is caused by a spinal glomus type (type 2) intramedullar arteriovenous malformation (AVM) at Th10-12 level. Venous hypertension is considered as the underlying factor of subarachnoid hemorrhage associated with spinal AVM. We aimed to present a spinal glomus type (type 2) intramedullary AVM that presented with nonperimesencephalic subarachnoid hemorrhage accompanied by the literature. © 2014 Wolters Kluwer Health, Inc. All rights reserved.en_US
dc.identifier.doi10.1097/WNQ.0000000000000059en_US
dc.identifier.endpage357en_US
dc.identifier.issn1050-6438
dc.identifier.issue3en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage355en_US
dc.identifier.urihttps://dx.doi.org/10.1097/WNQ.0000000000000059
dc.identifier.urihttps://hdl.handle.net/20.500.12684/756
dc.identifier.volume25en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherLippincott Williams and Wilkinsen_US
dc.relation.ispartofNeurosurgery Quarterlyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectarteriovenous malformation; subarachnoid hemorrhage; venous hypertensionen_US
dc.titleThoracolumbar Glomus-type Intramedullary Arteriovenous Malformations Presenting with Nonperimesencephalic Subarachnoid Hemorrhage: A Case Reporten_US
dc.typeArticleen_US

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