Miyake Shigeta, Kee Tze P, Falzon Andrew, Andrade Hugo, Krings Timo
Department of Neurosurgery, Yokohama City University School of Medicine, Yokohama, Kanagawa, Japan.
Division of Neuroradiology, Department of Medical Imaging, Joint Department of Medical Imaging, University Health Network and Toronto Western Hospital, University of Toronto, ON, Canada.
Interv Neuroradiol. 2024 Jun 7:15910199241260758. doi: 10.1177/15910199241260758.
Cavernous sinus dural arteriovenous fistula can cause cerebral edema and hemorrhage due to cortical venous reflux and congestion. Understanding complex venous reflux and drainage routes is crucial for treatment planning. Here, we present a case of a cavernous sinus dural arteriovenous fistula with cortical venous reflux via two separate terminations of the telencephalic veins caused by an aplastic basal vein of Rosenthal. The patient presented with diplopia and eye redness and was diagnosed with a Cognard type IIa + b cavernous sinus dural arteriovenous fistula. The shunt was supplied by the dural branches of the internal and external carotid arteries. Multiple shunt points involving the intercavernous sinus and the medial aspect of the left cavernous sinus were identified, with drainage into the supraorbital and intracranial veins, including two separate terminations of the telencephalic veins, one leading to the laterocavernous sinus via the superficial middle cerebral vein and the other to the cavernous sinus via the uncal vein, resulting in basal ganglia venous congestion in the absence of the basal vein of Rosenthal. During transvenous embolization, the intracranial veins, cavernous sinus, and intercavernous sinus were obliterated using a double-catheter technique with a combination of coils and liquid embolics. Telencephalic venous variations can lead to cavernous sinus drainage into the basal ganglia and orbitofrontal brain. This unique drainage pattern underscores the importance of recognizing anatomical variations when managing cavernous sinus dural arteriovenous fistula.
海绵窦硬脑膜动静脉瘘可因皮质静脉反流和淤血导致脑水肿和出血。了解复杂的静脉反流和引流途径对于治疗方案的制定至关重要。在此,我们报告一例海绵窦硬脑膜动静脉瘘,其通过罗森塔尔基底静脉发育不全导致的大脑静脉两个独立终末支出现皮质静脉反流。患者表现为复视和眼红,被诊断为Cognard IIa + b型海绵窦硬脑膜动静脉瘘。分流由颈内动脉和颈外动脉的硬脑膜分支供血。发现多个分流点,涉及海绵间窦和左侧海绵窦内侧,引流至眶上静脉和颅内静脉,包括大脑静脉的两个独立终末支,一支经大脑中浅静脉通向海绵窦外侧,另一支经钩静脉通向海绵窦,在没有罗森塔尔基底静脉的情况下导致基底节静脉淤血。在经静脉栓塞过程中,采用双导管技术,联合使用弹簧圈和液体栓塞剂闭塞颅内静脉、海绵窦和海绵间窦。大脑静脉变异可导致海绵窦引流至基底节和眶额部脑区。这种独特的引流模式强调了在处理海绵窦硬脑膜动静脉瘘时识别解剖变异的重要性。