Graduate School of Health Sciences, Medical School of Hacettepe University, Ankara, Turkey.
Department of Neurology, Medical School of Hacettepe University, Ankara, Turkey.
JAMA Neurol. 2015 Feb;72(2):217-8. doi: 10.1001/jamaneurol.2014.2077.
Dural arteriovenous fistula is a very rare cause of myelitis that can only be treated interventionally or surgically.
A man in his 30s with paraparesis and urinary incontinence had a long-segment thoracic lesion on spinal magnetic resonance imaging. Transverse myelitis was the initial diagnosis. Although a pulse steroid and intravenous immunoglobulin treatment regimen was given, no definite clinical response was seen. A spinal angiogram was performed in our center demonstrating right T7 to T8 spinal dural arteriovenous fistula. The fistula was occluded with embolization and the patient showed recovery following the endovascular treatment.
Myelitis usually is known to respond well to immunosuppressive treatments. Despite adequate medical treatment, if slow progression is seen in the follow-up clinically and radiologically, dural arteriovenous fistulas should be kept in mind in the etiopathogenesis.
硬脑膜动静脉瘘是一种非常罕见的脊髓炎病因,只能通过介入或手术治疗。
一名 30 多岁的男性出现截瘫和尿失禁,脊髓磁共振成像显示长节段胸段病变。最初诊断为横贯性脊髓炎。虽然给予了脉冲类固醇和静脉注射免疫球蛋白治疗方案,但未见明确的临床反应。在我们中心进行了脊髓血管造影,显示右侧 T7 至 T8 脊髓硬脑膜动静脉瘘。通过栓塞闭塞瘘管,患者在血管内治疗后恢复。
脊髓炎通常对免疫抑制治疗反应良好。尽管进行了充分的药物治疗,如果在随访中临床和影像学上出现缓慢进展,应在病因学上考虑硬脑膜动静脉瘘。