Kim Michael G, Jeong Seung W, Solli Elena, Amin Anubhav G, Ronecker Jennifer S, Bobra Shalabh
1Department of Neurosurgery, Westchester Medical Center, Valhalla, NY USA.
2New York Medical College, Valhalla, NY USA.
Spinal Cord Ser Cases. 2018 Jan 24;4:10. doi: 10.1038/s41394-018-0039-x. eCollection 2018.
A spinal dural arteriovenous fistula is a rare type of vascular malformation. If left untreated, these fistulas can result in significant neurological deficits secondary to spinal cord infarct or hemorrhage.
A 70-year-old female with a longstanding history of episodic progressive bilateral lower extremity weakness and sensory disturbances was previously misdiagnosed with multiple sclerosis. Imaging revealed a T2 signal change from T7 to the conus with associated signal change and she subsequently underwent a T10-L1 laminectomy for clip ligation of a spinal dural arteriovenous fistula. Here we present the clinical and radiographic progression of one patient with a spinal dural arteriovenous fistula.
Spinal dural arteriovenous fistulas are a rare but treatable cause of myelopathy, so it is important to understand its natural progression and radiologic findings as it is frequently misdiagnosed.
脊髓硬脊膜动静脉瘘是一种罕见的血管畸形类型。如果不进行治疗,这些瘘管可导致继发于脊髓梗死或出血的严重神经功能缺损。
一名70岁女性,有长期发作性进行性双侧下肢无力和感觉障碍病史,此前被误诊为多发性硬化症。影像学检查显示从T7至圆锥有T2信号改变及相关信号变化,随后她接受了T10-L1椎板切除术,以夹闭脊髓硬脊膜动静脉瘘。在此,我们展示了一名脊髓硬脊膜动静脉瘘患者的临床和影像学进展情况。
脊髓硬脊膜动静脉瘘是一种罕见但可治疗的脊髓病病因,因此了解其自然进展和影像学表现很重要,因为它经常被误诊。