Takeda N, Fujita S, Kondo T, Yasuda M, Nakamura M
Department of Neurosurgery, Himeji Brain and Heart Center, Hyogo, Japan.
No Shinkei Geka. 1987 Sep;15(9):1025-30.
Dural arteriovenous malformations (AVMs) are not uncommon. But most of dural AVMs are located in the cavernous portion or the transverse-sigmoid portion. Dural AVMs in the anterior fossa and very rare. We experienced a case of dural AVM in the anterior fossa and review 17 cases of dural AVM in the anterior fossa in the literature.
a 62-year-old male was admitted to our center because of unconsciousness and vomiting on Sept. 28; 1985. For nineteen months he had been on anticoagulant therapy after aorto-coronary bypass. Neurological examination on admission revealed somnolence and right-hemiparesis. CT scan revealed intracerebral hematoma in the left frontal lobe with ventricular perforation. Enhanced CT scan revealed patchy enhancement in the tip of the left frontal lobe. Selective angiographies were performed. Dural AVM, fed by both anterior ethmoidal arteries and drained by the cortical veins into the superior sagittal sinus and left superficial middle cerebral vein, was found. Selective external carotid angiography failed to visualize any AVM. MRI revealed spotty low signal intensity in the frontal tip by inversion recovery and spin echo. After admission his consciousness and right-hemiparesis improved completely. Left frontal craniotomy was done. On opening the dura, aneurysmal dilatation was found in the left frontal lobe, arising from the inner surface of the dura at the antero-medial corner of the left anterior fossa. From this aneurysmal dilatation a few veins entered the superior sagittal sinus. Red veins including aneurysmal dilation was removed from its origin together with the intracerebral hematoma. (ABSTRACT TRUNCATED AT 250 WORDS)
硬脑膜动静脉畸形(AVM)并不罕见。但大多数硬脑膜AVM位于海绵窦段或横窦-乙状窦段。前颅窝的硬脑膜AVM非常罕见。我们诊治了1例前颅窝硬脑膜AVM,并复习了文献中17例前颅窝硬脑膜AVM的病例。
一名62岁男性于1985年9月28日因意识不清和呕吐入住我院。在接受主动脉冠状动脉搭桥手术后的19个月里,他一直在接受抗凝治疗。入院时神经系统检查发现嗜睡和右侧偏瘫。CT扫描显示左额叶脑内血肿并破入脑室。增强CT扫描显示左额叶尖端有斑片状强化。进行了选择性血管造影。发现硬脑膜AVM,由筛前动脉供血,经皮质静脉引流至上矢状窦和左大脑中浅静脉。选择性颈外动脉造影未显示任何AVM。MRI通过反转恢复和自旋回波显示额叶尖端有斑点状低信号强度。入院后,他的意识和右侧偏瘫完全恢复。进行了左额叶开颅手术。打开硬脑膜后,在左额叶发现动脉瘤样扩张,起源于左前颅窝前内侧角硬脑膜的内表面。从这个动脉瘤样扩张处有几条静脉进入上矢状窦。包括动脉瘤样扩张在内的迂曲静脉连同脑内血肿一起从其起源处切除。(摘要截短至250字)