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经下腔静脉重建术治疗的一种罕见的间歇性跛行病因:病例报告。

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

作者信息

Ali Barkat, Ali Rana M, Langsfeld Mark, Marek John

机构信息

Department of Surgery, Division of Vascular Surgery, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.

Department of Surgery, Division of Vascular Surgery, University of New Mexico Health Sciences Center, Albuquerque, NM, USA.

出版信息

Int J Surg Case Rep. 2015;14:69-71. doi: 10.1016/j.ijscr.2015.07.016. Epub 2015 Jul 26.

Abstract

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.

摘要

引言

下腔静脉发育不全是下腔静脉异常的罕见情况之一,多见于年轻患者,表现为不明原因的深静脉血栓形成(DVT)或双侧下肢静脉功能不全无法解释。我们报告一例经下腔静脉重建治疗的下腔静脉发育不全病例。

病例

我们描述了一名28岁男性,双侧下肢静脉曲张伴疼痛,有右下肢DVT病史,正在接受华法林抗凝治疗。检查发现他双侧大隐静脉(GSV)广泛且右股静脉反流,双侧深静脉通畅。他接受了双侧GSV消融和微静脉切除术。六周后,他出现急性双侧髂股DVT,通过双侧腘静脉途径用组织纤溶酶原激活剂tPA溶栓治疗,这有助于缓解他的腿部肿胀,但他仍有使人衰弱的静脉性跛行。计算机断层扫描(CT扫描)显示DVT已消退,但发现下腔静脉发育不全。他接受了人工血管下腔静脉重建术,这有助于完全缓解他长期使人衰弱的双侧下肢跛行。

结论

对于有下肢静脉高压严重表现(即水肿、静脉曲张和DVT)的年轻患者,应考虑中央静脉异常。下腔静脉发育不全的严重症状性病例可通过下腔静脉重建治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3905/4573602/afa60d63e460/gr1.jpg

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