Huna-Baron R, Setton A, Kupersmith M J, Berenstein A
Sheba Medical Center, Tel Aviv, Israel.
Br J Ophthalmol. 2000 Jul;84(7):771-4. doi: 10.1136/bjo.84.7.771.
Orbital arteriovenous malformations (OAVM) are rare, mostly described with high flow characteristics. Two cases are reported with an OAVM of distinct haemodynamic abnormality. The clinical, angiographic features, and the management considerations are discussed.
Case review of two patients with dural AVM (DAVM) who presented to referral neuro-ophthalmology and endovascular services because of clinical symptoms and signs consistent with a cavernous sinus dural AVM.
In each patient, superselective angiography revealed a small slow flow intraorbital shunt supplied by the ophthalmic artery. The transarterial and transvenous endovascular approaches to treat the malformation were partially successful. Although, the abnormal flow was reduced, complete closure of the DAVM could not be accomplished without significant risk of iatrogenic injury. Neither patient's vision improved after intervention.
A DAVM in the orbit can cause similar clinical symptoms and signs to those associated with a cavernous sinus DAVM. Even with high resolution magnetic resonance imaging, only superselective angiography can identify this small intraorbital slow flow shunt. The location in the orbital apex and the small size precludes a surgical option for treatment. The transarterial and transvenous embolisation options are limited.
眼眶动静脉畸形(OAVM)较为罕见,大多表现为高流量特征。本文报告两例具有独特血流动力学异常的OAVM病例,并对其临床、血管造影特征及治疗考虑因素进行讨论。
回顾两例因临床症状和体征符合海绵窦硬脑膜动静脉畸形(DAVM)而转诊至神经眼科和血管内治疗科室的患者病例。
在每例患者中,超选择性血管造影显示由眼动脉供血的小的低流量眶内分流。经动脉和经静脉血管内治疗畸形的方法部分成功。尽管异常血流减少,但在无显著医源性损伤风险的情况下无法完全闭合DAVM。干预后两例患者的视力均未改善。
眼眶内的DAVM可引起与海绵窦DAVM相似的临床症状和体征。即使采用高分辨率磁共振成像,只有超选择性血管造影才能识别这种小的眶内低流量分流。位于眶尖且体积小排除了手术治疗的选择。经动脉和经静脉栓塞治疗的选择有限。