AI Article Synopsis

  • - A rare case of a dural arteriovenous fistula (DAVF) is reported in a young woman who experienced recurrent syncope over nine years without any other symptoms.
  • - The episodes of fainting were triggered by changes in position, physical exertion, and emotional stress, lasting from 2 to 3 hours after waking.
  • - The DAVF was successfully treated through endovascular embolization, resulting in no further episodes of syncope, thus highlighting the potential for DAVF to present primarily as syncope, a previously undocumented occurrence.

Article Abstract

Background: Dural arteriovenous fistulas (DAVFs) are pathologic vascular connections that shunt dural arterial flow directly to dural venous drainage. Only a few isolated case reports describe syncope on presentation. We report the first case of DAVF causing recurrent, progressive syncope in an otherwise asymptomatic patient.

Case Report: A female in her late 20s presented with a 9-year history of syncopal episodes and was found to have a DAVF. Syncopal episodes were exacerbated by positional changes, strenuous activity and emotional stressors. Symptoms occurred upon wakening and lasted for 2 to 3 hours before she was able to regain functionality. Physical examination revealed no abnormalities. Magnetic resonance imaging of the brain showed no irregularities. Magnetic resonance angiography revealed abnormal serpiginous structures in the left jugular foramen which communicated with the ascending pharyngeal branch of the left external carotid artery. Cerebral angiogram disclosed a left jugular bulb DAVF supplied by the left ascending pharyngeal and left occipital arteries. The DAVF was successfully managed by progressive endovascular embolization with coils and Onyx 34. On clinical follow-up evaluation, the patient had no further episodes of dizziness or syncope.

Conclusion: We present an atypical case of DAVF in a patient presenting with recurrent syncope. Only 4 cases of DAVF causing syncope have been reported, all in combination with other neurological symptoms. In comparison, we report a unique case of DAVF presenting solely with recurrent syncope, a previously undocumented finding in the literature. Our case adds to other reports of nonspecific DAVF presentations and highlights the importance of considering this etiology.

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Source
http://dx.doi.org/10.1097/NRL.0000000000000322DOI Listing

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