Dural arteriovenous fistulas (DAVFs) are vascular anomalies that form a connection between meningeal vessels and dural venous sinuses or cortical veins. A 47-year-old female with a history of rheumatoid arthritis and hypercoagulable state treated with warfarin was found to have a large transverse sinus DAVF with high-flow fast arteriovenous shunting. Her initial diagnostic angiogram performed at an outside institution clearly showed the large DAVF. Eight months later, a second diagnostic angiogram demonstrated that her DAVF had spontaneously resolved. Spontaneous regression of a DAVF is rare, and this is the largest DAVF that our institution has seen to resolve on its own. DAVFs have previously been known to spontaneously resolve, but few cases have been reported since it was first described in 1976. The mechanism for spontaneous closure is unknown, but several different mechanisms have been proposed. We postulate that spontaneous regression in this patient is related to her underlying hypercoagulable state and the high-flow nature of the DAVF. High-flow DAVFs can resolve spontaneously, and cautious modification of anticoagulation in select patients in order to induce fistula thrombosis may provide an avenue of management to consider. Her past medical history is significant for rheumatoid arthritis and the above-mentioned hypercoagulable state, as well as a remote history of several DVTs. She has no history of smoking, other tobacco use, alcohol use, or illicit drug use. Her brother is also noted to have a hypercoagulable state.Although the patient was prescribed a low molecular weight heparin bridge between her usual warfarin and the time of angiography at our institution, that prescription was not filled. Thus, the patient's warfarin was stopped four days prior to her procedure with no anticoagulant bridging. Upon presentation to our institution,
Case PresentationIntracranial dural arteriovenous fistulas (DAVFs) are rare vascular malformations that connect meningeal arteries to dural venous sinuses or cortical veins. They were originally believed to be benign lesions compared to pial arteriovenous malformations (AVMs) until intracranial hemorrhage from a DAVF was observed [1]. Although hemorrhage from ruptured cortical venous varices is the most serious and worrisome complication, DAVFs can present with a variety of symptoms, including headaches, seizures, pulsatile tinnitus, and vision disturbances. Few DAVFs have been reported to resolve spontaneously since the phenomenon was first described in 1976 [2]. The reason for spontaneous closure is largely unknown, although several mechanisms have been proposed. In this report, we describe a case of spontaneous resolution of a large DAVF in a patient with a hypercoagulable state.A 47-year-old female was seen at an outside institution and found to have a large transverse sinus DAVF with high-flow fast arteriovenous shunting. One year prior to discovery of the DAVF, she underwent work-up at an outside institution for a seven-year history of daily occipital he...