Morimoto Takayuki, Fujimoto Kenta, Ko Sungchul, Nishioka Toshikazu, Tokunaga Hidemori
Department of Neurosurgery, Nara City Hospital, Nara, Japan.
Department of Neurosurgery, Nara Prefecture General Medical Center, Nara, Japan.
Surg Neurol Int. 2024 Sep 27;15:351. doi: 10.25259/SNI_736_2024. eCollection 2024.
Spontaneous direct vertebral artery-external vertebral venous plexus (VA-EVVP) fistula is a rare disease that presents in patients with neurofibromatosis type 1 (NF-1) or trauma.
An 82-year-old female patient with no neurological deficits or trauma presented to our hospital with right hemianopsia. Head magnetic resonance imaging (MRI) revealed left occipital cerebral infarction and magnetic resonance angiography demonstrated high signal intensity in the left transverse sinus (TS). The attending doctor diagnosed an old infarction on the left occipital lobe and dural arteriovenous fistula (AVF) in the TS. After 3 years after the first diagnosis, her new attending doctor re-checked the MRI and performed digital subtraction angiography (DSA). The DSA examination revealed a single-hole AVF between the vertebral artery and external vertebral plexus at the C2 level, which was diagnosed as upper cervical VA-EVVP. The patient presented with tinnitus due to a high-flow VA-EVVP fistula, so we performed coil embolization of the fistula under general anesthesia using a double-catheter technique and achieved subtotal embolization, which diminished the intracranial reflux. The 6-month follow-up DSA image revealed complete obliteration of the AVF.
We report a rare case of upper cervical VA-EVVP fistula in a patient with no history of trauma and relevant medical conditions. Coil embolization of the fistula was performed using a combination of balloon-assisted and double-catheter techniques. Although the patient showed residual shunt flow after the intervention, follow-up DSA revealed complete obliteration. These findings should provide novel insights for the treatment strategy against VA-EVVP fistula.
自发性直接椎动脉-椎外静脉丛(VA-EVVP)瘘是一种罕见疾病,见于1型神经纤维瘤病(NF-1)患者或有创伤史的患者。
一名82岁女性患者,无神经功能缺损或创伤史,因右侧偏盲入住我院。头部磁共振成像(MRI)显示左侧枕叶脑梗死,磁共振血管造影显示左侧横窦(TS)高信号。主治医生诊断为左侧枕叶陈旧性梗死和TS硬脑膜动静脉瘘(AVF)。首次诊断3年后,她的新主治医生复查了MRI并进行了数字减影血管造影(DSA)。DSA检查显示C2水平椎动脉与椎外静脉丛之间存在单孔AVF,诊断为上颈椎VA-EVVP。该患者因高流量VA-EVVP瘘出现耳鸣,因此我们在全身麻醉下使用双导管技术对瘘进行了弹簧圈栓塞,实现了次全栓塞,减少了颅内反流。6个月随访DSA图像显示AVF完全闭塞。
我们报告了一例无创伤史和相关病史患者的罕见上颈椎VA-EVVP瘘病例。采用球囊辅助和双导管技术联合对瘘进行弹簧圈栓塞。尽管患者干预后仍有残余分流,但随访DSA显示完全闭塞。这些发现应为VA-EVVP瘘的治疗策略提供新的见解。