A rare case of arteriovenous malformation of the forearm

Crina V. Onciu , Jacopo Maffeis , Ion-Andrei Popescu , Frédéric Teboul
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引用次数: 0

Abstract

A 40-year-old man with a long-standing history of congenital arteriovenous malformation in his right forearm was seen with a large, pulsatile tumour in the hypothenar region extending with multiple tortuous vessels on the volar side of the forearm to the elbow crease. Preoperative Allen test and normal preoperative finger pressure measurement showed revascularization of the hand via radial artery. Ultrasonography, MRI and angiography described an arteriovenous malformation (AVM) type 4 Yakes, suggesting high risk for embolization. Surgical intervention with meticulous dissection and ulnar nerve release was performed in order to prevent important blood loss, distal ischemia and to preserve upper limb functionality. Surgical resection resulted in full recovery.

前臂动静脉畸形的罕见病例
一名 40 岁男子的右前臂患有先天性动静脉畸形,病史已久,就诊时发现下臂区域有一个巨大的搏动性肿瘤,肿瘤在前臂伏侧有多条迂曲的血管延伸至肘窝。术前艾伦测试和正常的术前指压测量显示,手部经桡动脉血管再通。超声波检查、核磁共振成像和血管造影显示该患者为亚克4型动静脉畸形(AVM),栓塞风险很高。为了防止严重失血和远端缺血,并保护上肢功能,医生对该患者进行了手术干预,细致剥离并松解尺神经。手术切除后患者完全康复。
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CiteScore
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