Renner Christof, Helm Jochen, Roth Henrik, Meixensberger Jürgen
Department of Neurosurgery, University of Leipzig, 04103 Leipzig, Germany.
Surg Neurol. 2006 May;65(5):506-10. doi: 10.1016/j.surneu.2005.06.022.
Intracranial dural arteriovenous malformations draining into the perimedullary venous system are rare lesions. In these cases, the selective spinal catheterization of all vessels with potential of causing that malformation was negative, and additional cerebral angiography usually reveals the fistula. Because of venous congestion of the cord caused by the DAVF, a delayed drainage or stagnation of contrast material in the artery of Adamkiewicz was considered as a compelling angiographic disorder so far.
We report about a 58-year-old patient with a DAVF of the right posterior fossa draining into the cervical and upper thoracic plexus of medullary veins, followed by progressive cervical myelopathy and a normal venous drainage of the artery of Adamkiewicz. Because of the failing endovascular treatment option, the neurosurgical intervention was performed. The fistula was explored and clipped without any complications. Immediately after operation, the patient reported an improvement of his neurological deficits.
About 38 cases of intracranial DAVFs draining into the perimedullary venous system are reported, but to our knowledge, this is the second one with a normal drainage of the artery of Adamkiewicz. The pathophysiological mechanisms, diagnostic procedures, and treatment modalities are discussed.
引流至髓周静脉系统的颅内硬脑膜动静脉畸形是罕见病变。在这些病例中,对所有可能导致该畸形的血管进行选择性脊髓导管造影均为阴性,而额外的脑血管造影通常能显示瘘口。由于硬脑膜动静脉瘘导致脊髓静脉充血,迄今为止,Adamkiewicz动脉造影剂延迟引流或停滞被视为一种明显的血管造影异常。
我们报告一名58岁患者,其右后颅窝硬脑膜动静脉瘘引流至颈髓和上胸段髓周静脉丛,继发进行性颈髓病,且Adamkiewicz动脉静脉引流正常。由于血管内治疗方案无效,遂进行了神经外科干预。探查并夹闭了瘘口,未出现任何并发症。术后患者立即报告神经功能缺损有所改善。
据报道,约有38例颅内硬脑膜动静脉瘘引流至髓周静脉系统,但据我们所知,这是第二例Adamkiewicz动脉引流正常的病例。本文讨论了其病理生理机制、诊断方法和治疗方式。