Sánchez-Morales Germán E, Anaya-Ayala Javier E, Serrano-Cueva María A, Salas-Torrez Eladio, Hinojosa Carlos A
* Department of Surgery, Mexico City, Mexico.
‖ Universidad Nacional Autonoma de Mexico, Mexico City, Mexico.
J Hand Surg Asian Pac Vol. 2019 Mar;24(1):89-92. doi: 10.1142/S2424835519720019.
Parkes Weber Syndrome (PWS) is a congenital disorder characterized by the presence of arteriovenous malformations (AVMs) in upper or lower extremities. We herein present a 35 year-old male with PWS with complex AVMs in the right upper extremity; he had been previously treated with multiple sessions of vessel embolization, sclerotherapy and AVM resections. The patient presented to our clinic with two month history of progressive hand ischemia, digit necrosis and infection. Angiography was performed demonstrating numerous AVMs and filiform flow through the ulnar artery with poor opacification of arterial structures in the hand. Because of advanced ischemia, soft tissue infection and osteomyelitis, a distal forearm amputation was indicated. Hand threatening ischemia secondary to steal phenomenon associated to AVMs in PWS is rarely encountered and reported. This case illustrates a complex clinical presentation with advanced disease that required limb amputation.
帕克斯·韦伯综合征(PWS)是一种先天性疾病,其特征是上肢或下肢存在动静脉畸形(AVM)。我们在此报告一名35岁患有PWS的男性,其右上肢存在复杂的AVM;他此前曾接受过多次血管栓塞、硬化治疗和AVM切除术。该患者因进行性手部缺血、手指坏死和感染两个月前来我院就诊。血管造影显示有大量AVM,通过尺动脉有丝状血流,手部动脉结构造影剂充盈不佳。由于严重缺血、软组织感染和骨髓炎,建议行前臂远端截肢术。PWS中与AVM相关的盗血现象继发的威胁手部的缺血很少见且鲜有报道。本病例说明了一种需要截肢的晚期疾病的复杂临床表现。