IntroductionSpinal vascular malformations are rare and often misdiagnosed entities. In principle, we distinguish between three types of spinal vascular malformation: extradural, dural, and intradural [2,6,7,11,12]. The intradural malformations can be separated into perimedullary fistulas and the real intramedullary arteriovenous malformations (AVMs). Intradural AVMs are supplied by spinal-cord supplying arteries, whereas dural malformations are supplied by meningeal arteries as branches of the radicular artery [6,12]. Eighty percent of all spinal AVMs are dural fistulas. In contrast to the probably inborn perimedullary fistulas, dAVFs are most likely acquired [11,12]. The fistula itself is located in the dural layer near the penetration point of the nerve root. Venous drainage runs along the spinal cord veins on the surface of the cord, because the local radicular venous drainage is missing. The high venous pressure is presumed to be the cause of clinical symptoms [2,6,9,11].Abstract Spinal dural arteriovenous fistula (dAVFs) are rare and often misdiagnosed entities. The choice between surgical treatment and embolization remains a matter of debate. We report on the cases of 18 patients (16 men, 2 women) with dAVF, who were treated surgically over an 11-year period. Patient age ranged from 32 to 84 years (mean 60 years). Six patients underwent embolization preoperatively. In three cases, angiography examinations failed to show feeding arteries on first examination at neuroradiological centers. Feeding arteries were at a different level than the fistula point in seven patients, two of them presenting with new anastomoses after embolization. Location of the fistula was midthoracic to lumbar. Seven patients were variously misdiagnosed with tumor, polyneuropathy, Guillain-Barré syndrome, syringomyelia, and knee disease. Clinical history was characterized by slowly progressive and fluctuating deterioration.Initial symptoms were mainly sensory loss and motor weakness, lasting for between 4 and 45 months before diagnosis (mean 15 months). Recurrent fistula after operation was found in one patient. In another patient, control angiography revealed a fistula at another level, and in a third, a fistula on the contralateral side. All three patients underwent reoperation. Temporary clinical deterioration was found in four patients, seven remained unchanged, and seven improved postoperatively. An attempt at embolization should be made following diagnostic angiography. Otherwise, surgery is our recommended treatment for spinal dural fistulas, as it has a lower failure rate. Because of the progressive natural course with severe deficits, we favor an early definitive treatment.