Âé¶¹´«Ã½Ó³»­

Âé¶¹´«Ã½Ó³»­

Explore the latest content from across our publications

Log In

Forgot Password?
Create New Account

Loading... please wait

Abstract Details

Acute Myelopathy Due to Intracranial Dural Arterio-Venous Fistula: A Case Report.
Cerebrovascular Disease and Interventional Neurology
Cerebrovascular Disease and Interventional Neurology Posters (7:00 AM-5:00 PM)
105
N/A

Intracranial dural arterio-venous fistula (DAVF) with spinal venous drainage is a rare clinical entity often underdiagnosed in the setting of unrevealing spinal angiography in a patient presenting with myelopathy. Here we present a case of a patient with acute myelopathy due to intracranial DAVF with spinal drainage who underwent successful Onyx embolization. 

A 28 year-old man presented with an acute onset of peri-rectal numbness and urinary retention, followed by right lower extremity weakness and left-sided paraesthesia. Initial examination revealed decreased sensation to all modalities in the right face and left hemibody, right lower extremity weakness, and diffuse hyperreflexia with positive Babinski and Hoffman signs bilaterally. Magnetic Resonance Imaging (MRI) revealed a T2 hyperintensity in the spinal cord and extensive flow-voids from dilated pial vessels throughout the thoracic and cervical central canal extending through the craniocervical junction. Digital subtraction angiography (DSA) of the cerebral arteries demonstrated an intracranial DAVF fed by the meningohypophyseal branch of the left internal carotid artery. The patient underwent a successful Onyx embolization with complete resolution of the urinary retention and gradual improvement of motor weakness.  

The incidence of intracranial DAVFs is 10-15% of all intracranial vascular malformations.  DAVF classification is based on its venous drainage.  Clinical presentation with spinal venous drainage includes insidious onset of progressive myelopathy with paraesthesia, motor weakness, gait abnormality, and sphincter dysfunction. MRI typically reveals diffuse intramedullary T2 hyperintensity and prominent serpiginous intradural extramedullary flow voids. DSA of the intracranial and spinal vasculature is the gold standard imaging modality of choice. Treatment includes endovascular or surgical occlusion.

DAVF is a rare but treatable cause of an otherwise progressive myelopathy. DSA is warranted in patients with MRI findings consistent with spinal DAVF, particularly with an unrevealing spinal angiogram.  

Authors/Disclosures

PRESENTER
No disclosure on file
Roua Kahila, MD (Orlando health) Dr. Kahila has nothing to disclose.
Jaspreet Johal, MD Dr. Johal has nothing to disclose.
Hussam A. Yacoub, DO (The Lehigh Valley Health Network) Dr. Yacoub has nothing to disclose.