A rare cause of claudication treated with IVC reconstruction: A case report

被引:10
作者
Ali, Barkat [1 ]
Rana, M. Ali [1 ]
Langsfeld, Mark [1 ]
Marek, John [1 ]
机构
[1] Univ New Mexico, Hlth Sci Ctr, Dept Surg, Div Vasc Surg, Albuquerque, NM 87131 USA
关键词
IVC-Inferior Vena Cava; PTFE-Polytetrafluoroehtylene; DVT-Deep Vein Thrombosis;
D O I
10.1016/j.ijscr.2015.07.016
中图分类号
R61 [外科手术学];
学科分类号
摘要
INTRODUCTION: Inferior vena cava (IVC) agenesis is one of rare entities of IVC anomalies which presents in young patients with unprovoked deep venous thrombosis (DVT) or unexplained bilateral lower venous insufficiency. We are presenting a case of IVC agenesis which was treated with IVC reconstruction. CASE: We describe a case of 28 years old male with painful bilateral lower extremity varicose veins and a history of right lower extremity DVT and was on anticoagulation with warfarin. He was found to have extensive bilateral greater saphenous veins (GSVs) and right femoral vein reflux with patent bilateral deep veins. He was treated with bilateral GSV ablation and microphlebectomies. Six weeks later he presented with acute bilateral iliofemoral DVTs treated with tissue plasminogen activator thrombolysis tPA via bilateral popliteal vein access which helped relieve his leg swelling but he continued to have debilitating venous claudication. A computed tomography (CT scan) demonstrated resolution of DVT but revealed IVC agenesis. He underwent IVC reconstruction with prosthetic graft which helped complete resolution of his chronically debilitating bilateral lower extremity claudication. CONCLUSION: In young patients with severe manifestations of lower extremity venous hypertension i.e. edema, varicosity and DVT, central venous anomaly should be considered. Severely symptomatic cases of IVC agenesis can be treated with IVC reconstruction. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:69 / 71
页数:3
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