Department of Neurosurgery, 26807Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Department of Neurosurgery, 89421Tokyo Dental College Ichikawa General Hospital, Chiba, Japan.
Neuroradiol J. 2022 Oct;35(5):640-646. doi: 10.1177/19714009221096829. Epub 2022 Apr 28.
Pial arteriovenous fistula (AVF) is a vascular fistulous disease in which the cerebral pial artery and vein are directly connected without the intervening nidus within a sub-pial space. Multi-hole pial AVFs, wherein multiple feeders flow into one drainer, are usually formed with complex angioarchitecture and are difficult to treat.
A rare case of an adult patient with hereditary hemorrhagic telangiectasia and multi-hole pial AVF was described. A 23-year-old woman was referred to our hospital. She was previously diagnosed with left cerebellar pial AVF with multiple feeders (bilateral superior cerebellar artery and common trunk of the left anterior inferior cerebellar artery and posterior inferior cerebellar) and large varix that had been untreated for 9 years. The enlargement of the large varix with the new second varix formation was revealed by angiography. Although asymptomatic, considered to be a risk for future hemorrhage was the continuous high hemodynamic stress.
Endovascular embolization was performed by securing safe transarterial -butyl-2-cyanoacrylate injection by transarterial and transvenous coil placement to the shunt points and feeders, resulting in total occlusion of the fistula without any complications. Extensive transvenous coil placement inside the varix allowed safe embolization of the entire fistula with multiple high-flow feeders. Moreover, bidirectional (transarterial and transvenous) retrograde coil embolization enabled firm obliteration of the shunt points.
Performing combined transarterial and transvenous embolization in a well-balanced manner was considered to treat multi-hole pial AVF to provide a safe and effective embolization.
软膜动静脉瘘(AVF)是一种血管性瘘管疾病,其中脑软膜动脉和静脉直接相连,而没有在软膜下空间内的中间病灶。多孔软膜 AVF 中,多个供血动脉流入一个引流静脉,通常具有复杂的血管构筑,并且难以治疗。
描述了一例成人遗传性出血性毛细血管扩张症和多孔软膜 AVF 的罕见病例。一名 23 岁女性被转介至我院。她之前被诊断为左侧小脑软膜 AVF,伴多个供血动脉(双侧小脑上动脉和左侧前下小脑动脉及后下小脑动脉共干)和大静脉瘤,未经治疗 9 年。造影显示大静脉瘤增大并形成新的第二静脉瘤。尽管无症状,但持续的高血流动力学压力被认为是未来出血的风险。
通过经动脉和经静脉放置线圈至分流点和供血动脉,安全地进行了经动脉 -丁基-2-氰基丙烯酸酯栓塞,从而实现瘘管完全闭塞,无任何并发症。在静脉瘤内广泛放置经静脉线圈,允许安全栓塞具有多个高流量供血动脉的整个瘘管。此外,双向(经动脉和经静脉)逆行线圈栓塞使分流点得到牢固闭塞。
以平衡的方式进行联合经动脉和经静脉栓塞被认为是治疗多孔软膜 AVF 的一种安全有效的方法。