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Natural history, current concepts, classification, factors impacting endovascular therapy, and pathophysiology of cerebral and spinal dural arteriovenous fistulas.

TitleNatural history, current concepts, classification, factors impacting endovascular therapy, and pathophysiology of cerebral and spinal dural arteriovenous fistulas.
Publication TypeJournal Article
Year of Publication2014
AuthorsHacein-Bey, L., Konstas A. Aristeidis, & Pile-Spellman J.
JournalClin Neurol Neurosurg
Volume121
Pagination64-75
Date Published2014 Jun
ISSN1872-6968
KeywordsCavernous Sinus, Central Nervous System Vascular Malformations, Cerebral Angiography, Cerebrum, Embolization, Therapeutic, Humans, Spinal Cord
Abstract

Dural arteriovenous fistulas (DAVFs) may occur anywhere there is a dural or meningeal covering around the brain or spinal cord. Clinical manifestations are mostly related to venous hypertension, and may be protean, acute or chronic, ranging from minor to severe, from non-disabling tinnitus to focal neurological deficits, seizures, hydrocephalus, psychiatric disturbances, and developmental delay in pediatric patients. Although low-grade lesions may have a benign course and spontaneous involution may occasionally occur (i.e. cavernous sinus DAVFs), the risk of hemorrhage is considerable in high grade lesions. Angiographic features of DAVFs have been clarified since the 1970s when venous drainage pattern was clearly identified as the most significant risk predictor and as a major determinant of success or failure of treatment. The mainstay of therapy is interruption of arteriovenous shunting, which has traditionally been accomplished surgically. Currently, endovascular therapy is generally considered the first line of treatment, allowing elimination of the lesion in most patients, with surgery and stereotactic radiosurgery reserved for complex situations. This review discusses major aspects of DAVFs, including grading systems, clinical presentation, diagnostic evaluation, various issues impacting endovascular therapy, and pathophysiology.

DOI10.1016/j.clineuro.2014.01.018
Alternate JournalClin Neurol Neurosurg
PubMed ID24636717

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