Kikuchi K, Kowada M
Neurosurgical Service, Akita University Hospital, Japan.
Surg Neurol. 1994 Jan;41(1):56-64. doi: 10.1016/0090-3019(94)90209-7.
Two cases of dural arteriovenous malformation (AVM) involving the base of the anterior cranial fossa are reported. The nidi in both cases were located in the region of the left cribriform plate and mainly supplied by the anterior ethmoidal arteries of both sides, draining through pial veins into either the cavernous sinus or the superior sagittal sinus. In the first case neurologic symptoms resulted from transient frontal lobe dysfunction presumably due to abnormal venous drainage, and the second case presented with subarachnoid hemorrhage caused by rupture of dural AVM at the base of the anterior fossa. Both cases were surgically managed and the AVMs were successfully obliterated. This unique subgroup of dural AVM in the anterior fossa is thoroughly reviewed in the literature, and the epidemiology, symptomatology, neuroradiology, surgical treatment, and associated vascular lesions are discussed.
报告了两例累及前颅窝底部的硬脑膜动静脉畸形(AVM)。两例的病灶均位于左侧筛板区域,主要由双侧筛前动脉供血,经软脑膜静脉引流至海绵窦或上矢状窦。第一例患者出现短暂性额叶功能障碍,推测是由于异常静脉引流所致;第二例患者因前颅窝底部硬脑膜AVM破裂导致蛛网膜下腔出血。两例均接受了手术治疗,AVM均成功闭塞。本文对文献中前颅窝硬脑膜AVM这一独特亚组进行了全面综述,并讨论了其流行病学、症状学、神经放射学、手术治疗及相关血管病变。