T2 MRA Lat RCC angiogram

Diagnosis: Pial arteriovenous malformation

Pial AVMs are thought to be congenital fed by branches of the intracranial circulation but may become mixed pial-dural if they parasitize the external carotid artery or muscular branches of the vertebrals. 98% of pial AVMs are solitary and 85% are supratentorial and may be multiple in Osler-Weber-Rendu and Wyburn-Mason syndromes. 10% are complicated by aneurysms and have an annual risk of bleeding of 2-4%. 1/2 present with hemorrhage, another 1/4 with seizures. This was a completely pial AVM with cortical venous drainage via the anastomotic veins of Trolard and Labbe. The presence of cortical (vs deep) venous drainage raises the risk of hemorrhage. Related Cases













































Dural AVF Pial AVM Vein of Galen malformation