Transvenous endovascular treatment for vein of Galen aneurysmal malformation with idiopathic bilateral sigmoid sinus occlusion.

Hengwei Jin, Xiangyu Meng, Jiale Quan, M. Lv, Chuhan Jiang
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引用次数: 1

Abstract

BACKGROUND Vein of Galen Malformations (VGAM) and bilateral idiopathic occlusion of the sigmoid sinuses are extremely rare. We report a child with Vein of Galen Aneurysmal Malformation (VGAM) and Idiopathic bilateral sigmoid sinus occlusion simultaneously, and managed through endovascular therapy in one session. This case highlights the coexistence of the lesions, as well as the one-session technical feasibility and good clinical outcome for endovascular treatment. CLINICAL PRESENTATION The child presented with enlarged head circumference and epilepsy. The frequency of seizure increased from one time to several times a day. CTA/CTV confirmed coexistence of Vein of Galen Malformations and idiopathic bilateral sigmoid sinus occlusion. CONCLUSION One session trans-venous approach was performed. The VGAM was completely occluded and the dominant sigmoid sinus was recanalized. Thirteen months telephone follow-up confirmed normal head growth. The patient is seizure-free and recovered very well with normal neurological and developmental condition. This study provides evidentiary support for one-session endovascular therapy in patient with VGAM and idiopathic bilateral sigmoid sinus occlusion.
经静脉血管内治疗特发性双侧乙状窦闭塞的盖伦静脉动脉瘤畸形。
背景:盖伦静脉畸形(VGAM)和双侧特发性乙状窦阻塞是非常罕见的。我们报告一个儿童同时患有盖伦静脉动脉瘤畸形(VGAM)和特发性双侧乙状窦闭塞,并通过一次血管内治疗进行治疗。本病例强调了病变的共存性,以及血管内治疗的一次性技术可行性和良好的临床效果。临床表现:患儿表现为头围增大和癫痫。癫痫发作的频率从一天一次增加到一天几次。CTA/CTV证实盖伦静脉畸形与特发性双侧乙状窦闭塞共存。结论经静脉入路1期。VGAM完全闭塞,优势乙状窦再通。13个月的电话随访证实头部发育正常。患者无癫痫发作,恢复良好,神经和发育状况正常。本研究为VGAM合并特发性双侧乙状窦闭塞患者的一次血管内治疗提供了证据支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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