Shi Zhong-Song, Ziegler Jordan, Gonzalez Nestor R, Feng Lei, Tateshima Satoshi, Jahan Reza, Duckwiler Gary, Viñuela Fernando
Division of Interventional Neuroradiology, University of California at Los Angeles Medical Center, Los Angeles, California 90095-1721, USA.
Neurosurgery. 2008 Feb;62(2):408-15; discussion 415. doi: 10.1227/01.neu.0000316007.34259.26.
Dural arteriovenous fistulae (DAVFs) rarely involve the clivus. This report examines the clinical presentation, angiographic findings, endovascular management, and outcome of clival DAVFs. Particular attention was given to safety and efficacy of transarterial embolization using liquid embolic agents.
We reviewed the clinical and radiological data of 10 patients with spontaneous clival DAVFs who were treated endovascularly at the University of California at Los Angeles Medical Center between 1992 and 2006.
Nine patients presented with ocular symptoms and one patient experienced pulsatile tinnitus. Cerebral angiograms showed that these clival DAVFs were supplied by multiple branches of the internal and external carotid arteries. The patterns of venous drainage were from the clival veins to the cavernous sinus and superior ophthalmic vein in nine patients and to the inferior petrosal sinus in two patients. Six clival DAVFs were embolized transarterially through the clival branches of the ascending pharyngeal artery. Onyx 18 (Micro Therapeutics Inc., Irvine, CA) was used in three patients and n-butyl cyanoacrylate was used in three patients. Immediate complete angiographic obliteration was achieved in three patients. All six patients experienced an angiographic and clinical cure without any complications at 3 months. Two patients were incompletely treated using particles and coils for the relief of the symptoms. Two other patients were completely treated after the recipient clival venous structures were occluded transvenously with coils.
Clival DAVFs can be misdiagnosed as dural cavernous sinus fistulae. The best treatment is transarterial embolization of the dural feeders using liquid embolic agents. Transvenous occlusion of the cavernous sinus is unnecessary in most cases.
硬脑膜动静脉瘘(DAVF)很少累及斜坡。本报告探讨斜坡DAVF的临床表现、血管造影表现、血管内治疗及预后。特别关注使用液体栓塞剂经动脉栓塞的安全性和有效性。
我们回顾了1992年至2006年间在加利福尼亚大学洛杉矶分校医学中心接受血管内治疗的10例自发性斜坡DAVF患者的临床和放射学资料。
9例患者出现眼部症状,1例患者有搏动性耳鸣。脑血管造影显示,这些斜坡DAVF由颈内动脉和颈外动脉的多个分支供血。9例患者的静脉引流模式为从斜坡静脉至海绵窦和眼上静脉,2例患者至岩下窦。6例斜坡DAVF经咽升动脉的斜坡分支进行经动脉栓塞。3例患者使用了Onyx 18(Micro Therapeutics Inc.,尔湾,加利福尼亚州),3例患者使用了正丁基氰基丙烯酸酯。3例患者立即实现了血管造影完全闭塞。所有6例患者在3个月时均实现了血管造影和临床治愈,无任何并发症。2例患者使用颗粒和线圈进行不完全治疗以缓解症状。另外2例患者在经静脉用线圈闭塞接受的斜坡静脉结构后得到完全治疗。
斜坡DAVF可能被误诊为硬脑膜海绵窦瘘。最佳治疗方法是使用液体栓塞剂经动脉栓塞硬脑膜供血动脉。大多数情况下无需经静脉闭塞海绵窦。