May-Thurner syndrome: diagnosis and management

Author:

Brazeau Nicholas F.1,Harvey Harlan B.2,Pinto Erique G.3,Deipolyi Amy2,Hesketh Richard L.4,Oklu Rahmi2

Affiliation:

1. Harvard University, Boston, MA, USA

2. Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA

3. Department of Imagiology, Hospital Professor Doutor Fernando Fonseca, Amadora, Portugal

4. Cardiff University School of Medicine, Cardiff, CF, UK

Abstract

For over fifty years, the pathogenesis of May-Thurner syndrome (MTS) has been associated with chronic left common iliac vein compression resulting in the formation of intraluminal, permanent obstructive lesions. However, despite this association, the mechanism by which compression produces these lesions is unknown. Diagnostic accuracy of MTS is critical since it often afflicts young patients requiring endovascular management. This review will focus on the historical, embryological and evolutionary description of MTS and examine its development, diagnosis, clinical management and potential diagnostic errors.

Publisher

Hogrefe Publishing Group

Subject

Cardiology and Cardiovascular Medicine

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