Seizure as the first symptom of cavernous sinus dural arteriovenous fistula: A case report and literature review

Mengxin Li, Shuai Jia, Jian Li, Jianhong Geng, Xiaojun Zhang, Yanqiang Wang
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Abstract

Cavernous sinus dural arteriovenous fistula (CS-DAVF) is an abnormal arteriovenous communication associated with a variety of clinical manifestations. The previous literature has rarely reported the occurrence of CS-DAVF with seizures and cerebral hemorrhage, signaling the need for more case reports and literature review in this area. A 62-year-old Chinese female presented with a paroxysmal loss of consciousness, accompanied with involuntary eye movement to the left, chewing issues, salivation at the right corner of the mouth, and bit tongue. The brain computed tomography revealed that the left temporal lobe was hemorrhagic. Brain scan and contrast-enhanced magnetic resonance imaging showed diffuse meningeal enhancement and lesions in the left frontoparietal temporal lobe, insular lobe, and hippocampal head region. Electroencephalography demonstrated continuous emission of spike and slow waves in the left hemisphere. With the aid of digital subtraction angiography, the patient was confirmed with a diagnosis of CS-DAVF draining into the ipsilateral cavernous sinus, intercavernous sinus, contralateral cavernous sinus, left superior ophthalmic vein, left lateral fissure vein, and left pterygoid venous plexus. The fistula was closed with interventional embolization through the femoral vein, and immediate angiography showed complete resolution of CS-DAVF after operation. The patient did not manifest any post-operative complications. This case highlights that the prevention of epilepsy, cerebral hemorrhage, and other serious complications is extremely important for good prognosis, especially in some patients presenting with serious clinical symptoms. It also sheds light on the necessity to consider the diagnosis of CS-DAVF if seizures, although extremely rare, are present.
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以癫痫为首发症状的海绵窦硬脑膜动静脉瘘1例报告并文献复习
海绵窦硬膜动静脉瘘(CS-DAVF)是一种与多种临床表现相关的异常动静脉通讯。既往文献很少报道CS-DAVF合并癫痫发作和脑出血的发生,这方面还需要更多的病例报道和文献综述。一名62岁中国女性,表现为阵发性意识丧失,伴眼球不自主向左移动,咀嚼问题,口腔右角流涎,舌咬。脑部电脑断层显示左颞叶出血。脑部扫描和磁共振增强成像显示弥漫性脑膜增强,左侧额顶叶颞叶、岛叶和海马区病变。脑电图显示左半球连续发射尖波和慢波。经数字减影血管造影证实,CS-DAVF引流至同侧海绵窦、海绵间窦、对侧海绵窦、左眼上静脉、左外侧裂静脉、左翼状静脉丛。经股静脉介入栓塞关闭瘘口,术后即刻血管造影显示CS-DAVF完全消退。患者未出现任何术后并发症。本病例强调预防癫痫、脑出血等严重并发症对预后极为重要,特别是对一些临床症状严重的患者。它还阐明了考虑CS-DAVF诊断的必要性,如果癫痫发作,虽然极其罕见,存在。
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