Olivero W C, Hanigan W C, McCluney K W
Division of Neurosurgery, University of Illinois College of Medicine, Peoria.
J Neurosurg. 1993 Jul;79(1):119-20. doi: 10.3171/jns.1993.79.1.0119.
A 16-year-old boy presented with acute midline thoracic pain followed by rapidly progressive paraplegia. The initial neurological examination demonstrated a complete sensory and motor paraplegia, which significantly improved spontaneously over the following 2 days. Magnetic resonance imaging revealed a posterior epidural hematoma extending from the T-4 to T-6 vertebrae, and spinal angiography demonstrated an arteriovenous malformation (AVM) with a nidus of abnormal epidural vessels at the level of the T-5 vertebra, which was confirmed surgically. This case represents one of the first reports of a spinal epidural AVM confirmed by angiography.
一名16岁男孩出现急性胸段中线疼痛,随后迅速发展为截瘫。初始神经系统检查显示完全性感觉和运动性截瘫,在接下来的2天内自发显著改善。磁共振成像显示硬膜外血肿从T4椎体延伸至T6椎体,脊髓血管造影显示在T5椎体水平有一个动静脉畸形(AVM),其病灶为异常的硬膜外血管,手术证实了这一点。该病例是经血管造影证实的脊髓硬膜外AVM的首批报告之一。