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Review Article
Mechanisms of Disease
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Volume 355:488-498 August 3, 2006 Number 5
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Chronic Venous Disease
John J. Bergan, M.D., Geert W. Schmid-Schönbein, Ph.D., Philip D. Coleridge Smith, D.M., Andrew N. Nicolaides, M.S., Michel R. Boisseau, M.D., and Bo Eklof, M.D., Ph.D.

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Chronic venous disease of the lower limbs is manifested by a range of signs, the most obvious of which are varicose veins and venous ulcers. However, the signs also include edema, venous eczema, hyperpigmentation of skin of the ankle, atrophie blanche (white scar tissue), and lipodermatosclerosis (induration caused by fibrosis of the subcutaneous fat) (Figure 1). Considerable progress has been made in understanding the mechanisms that underlie these diverse manifestations, in particular the role of inflammation. This article reviews these advances and places them in a clinical context.

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Figure 1. Clinical Manifestations of Chronic Venous Disease.

Telangiectases (clinical, etiologic, anatomical, . . . [Full Text of this Article]

 
The Scale of the Problem

Prevalence

Economic Impact

Symptoms and Quality of Life

Venous Hypertension

Valve and Vein-Wall Changes in Chronic Venous Disease

Changes in Venous Valves

Structural Changes in the Vein Wall

Role of Pressure and Shear Stress

The Role of Elevated Pressure

The Role of Shear Stress

Skin Changes

Chronic Inflammation

Mechanisms of Inflammation

The Link between Inflammation and Skin Changes

Implications for Treatment


Source Information

From the Departments of Surgery (J.J.B.) and Bioengineering (G.W.S.-S.), Whitaker Institute of Biomedical Engineering, University of California, San Diego, La Jolla; the Department of Vascular Surgery, Royal Free and University College Medical School, Middlesex Hospital, London (P.D.C.S.); the Department of Surgery, Imperial College London, University of Cyprus, and Vascular Screening and Diagnostic Centre, Nicosia, Cyprus (A.N.N.); the Department of Vascular Biology and Pharmacology, University of Bordeaux 2, Bordeaux, France (M.R.B.); and the Department of Surgery, University of Lund, Lund, Sweden (B.E.).

Address reprint requests to Dr. Bergan at 9850 Genesee, Suite 410, La Jolla, CA 92037, or at jbergan@ucsd.edu.


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