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伴行的动静脉畸形:一种罕见的临床实体。

Developmental venous anomaly coexisting with a true arteriovenous malformation: a rare clinical entity.

机构信息

Department of Radiology, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.

出版信息

J Neurointerv Surg. 2012 Jul;4(4):e19. doi: 10.1136/neurintsurg-2011-010016. Epub 2011 Jul 29.

DOI:10.1136/neurintsurg-2011-010016
PMID:21990487
Abstract

Two patients diagnosed with arteriovenous malformation (AVM) in close association with a developmental venous anomaly (DVA) are reported. The first patient presented with episodes of left extremity weakness and numbness as well as chronic headaches. The second patient presented with spontaneous intracerebral hemorrhage. Cerebral angiography showed that both the AVM and the transmedullary veins of the DVA drained through the transcortical vein. The AVMs were treated by highly selective transarterial embolization with Onyx embolic agent while preserving the DVAs. It is suggested that the cause of the presentation in both patients was secondary to the association of the AVM with the delicate hemodynamic balance and less robust angioarchitecture of the DVA.

摘要

现报道 2 例与发育性静脉异常(DVA)密切相关的动静脉畸形(AVM)患者。第 1 例患者表现为左肢无力和麻木以及慢性头痛。第 2 例患者表现为自发性脑出血。脑血管造影显示 AVM 和 DVA 的穿髓静脉均通过皮质静脉引流。使用 Onyx 栓塞剂对 AVM 进行高度选择性经动脉栓塞治疗,同时保留 DVA。这表明,2 例患者的表现原因是 AVM 与 DVA 的脆弱血流动力学平衡和不那么稳健的血管结构之间的关联。

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Atypical developmental venous anomaly associated with contrast enhancement and hyperperfusion in the surrounding basal ganglia.非典型发育性静脉异常,伴有周围基底节区对比增强和高灌注。
Quant Imaging Med Surg. 2015 Jun;5(3):472-5. doi: 10.3978/j.issn.2223-4292.2014.09.02.