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Comprehensive Endovascular and Open Surgical Management of Cerebral Arteriovenous Malformations
Published on: October 20, 2017
Angiographically Silent Ruptured Dural Arteriovenous Fistula Presenting As Subdural Hematoma
Zachary A Abecassis1, Guilherme Barros1, Laligam N Sekhar1
1Neurological Surgery, University of Washington, Seattle, USA.
Insights
Dural arteriovenous fistulas (dAVF) can cause serious neurological issues. This case highlights a ruptured dAVF presenting as a subdural hematoma, which was initially undetectable by standard cerebral angiography.
Area of Science:
- Neurology
- Vascular Surgery
- Radiology
Background:
- Dural arteriovenous fistulas (dAVF) are abnormal connections between dura mater arteries and veins.
- These malformations typically present with symptoms like headaches and can lead to severe neurological deficits.
- Diagnosis usually involves CT angiography (CTA) and catheter angiography.
Observation:
- A patient presented with a headache and a large holohemispheric subdural hematoma without a history of trauma.
- CT angiography revealed abnormal vessels near the temporal lobe, but a subsequent cerebral angiogram showed no early venous drainage.
- Surgical exploration identified an aberrant connection between a cortical vein and the middle meningeal artery.
Findings:
- The aberrant vascular connection was successfully ligated during surgery.
- This case demonstrates a rare instance where a ruptured dural arteriovenous fistula was radiographically occult on cerebral angiography.
- The subdural hematoma was evacuated, resolving the patient's symptoms.
Implications:
- Ruptured dural arteriovenous fistulas can present atypically, posing diagnostic challenges.
- Advanced imaging and intraoperative findings are crucial for diagnosing and treating such rare vascular malformations.
- This case underscores the importance of considering dAVFs even when initial angiography is negative.
Abstract:
Dural arteriovenous fistulas (dAVF) are aberrant vascular communications that can have devastating effects ranging from headaches to death. Typically, these malformations are identifiable on a CT angiogram (CTA) and confirmed via catheter angiography. We present a case of a female patient who presented with a headache and was found to have a large holohemispheric subdural hematoma. Given the lack of trauma, a CTA was performed. The CTA revealed abnormal vessels in the anterior temporal lobe spanning her hematoma. A diagnostic cerebral angiogram was performed; no early venous drainage was detected. When the patient was taken to the operating room for subdural hematoma evacuation, an aberrant connection from a superficial cortical vein to the middle meningeal artery was identified and ligated. Although rare, this case demonstrates that patients can present with ruptured vascular malformations that are radiographically silent on cerebral angiography.
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