Symptoms are most often caused by blockage of the cerebrospinal fluid flow and problems with the eye movement pathways. Headache, nausea and vomiting, and double vision are common.
Although AVMs are congenital (which means that patients are born with it), they are not hereditary (which means that they are not passed from parents to children). Most AVMs declare themselves by bleeding in adults younger than 40 years old. Some AVMs declare themselves by causing seizures or headaches. We attempt whenever possible to identify and eliminate AVMs before they bleed. We typically find the AVM in a computed tomography (CT) scan or, more commonly, in a magnetic resonance imaging (MRI) scan. If we find an AVM by CT or MRI, we then obtain an angiogram. At this point, the angiogram is the test that most accurately shows the AVM and its relationship to the surrounding arteries and veins.
At ANS, we treat AVMs using a combination of three methods, depending on the type of AVM:
- Microsurgical resection: During microsurgical resection, we perform a craniotomy and remove the AVM from the brain or spinal cord using a microscope.
- Stereotactic radiosurgery: During this treatment, we deliver a concentrated dose of radiotherapy to the core of the AVM in one session. Over the course of 2 to 5 years, the vessels of the AVM clot off and the AVM shuts down.
- Endovascular embolization: During this treatment, we pass a catheter through the groin up into the arteries in the brain that lead to the AVM and inject a material into these arteries. This injection shuts off that artery and reduces the flow of blood through the AVM. Endovascular embolization by itself typically does not eliminate the AVM and is therefore almost always used as a preliminary step in preparation for either microsurgical resection or stereotactic radiotherapy.