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Livedoid vasculopathy

Author: Vanessa Ngan, Staff Writer, 2004. Updated by A/Prof Amanda Oakley, January 2016.

What is livedoid vasculopathy?

Livedoid vasculopathy is a rare, chronic vascular disorder characterised by persistent painful ulceration of the lower extremities. The condition occurs chiefly but not exclusively on the lower leg or foot.

Livedoid vasculopathy was also known as ‘livedo vasculitis’, ‘livedoid vasculitis’ and ‘livedo reticularis with summer ulceration’. It is now clear that it is not primarily a vasculitis (inflammation of the blood vessel wall), but to occlusion of small blood vessels, hence the change in name.

Who gets livedoid vasculopathy?

Livedoid vasculopathy occurs most commonly in middle-aged women, but has been reported at all ages including childhood. There is often an increased incidence during the summer months and during pregnancy.

Some patients with livedoid vasculopathy have an associated conditions that predisposes them to occlusion of the small vessels of the lower leg. These include:

What is the cause of livedoid vasculopathy?

The exact cause of livedoid vasculopathy remains unclear, and various theories have been published referring to abnormalities within the blood vessel wall and in the circulating blood. It is likely that several different abnormalities may lead to clotting within small blood vessels of the lower legs. The thrombi result in necrosis of overlying skin, ulceration and very slow healing. There is no primary vasculitis.

Prothrombin G20210A gene mutation has been found in about 8% of patients.

What are the clinical features of livedoid vasculopathy?

Livedoid vasculopathy affects lower legs, ankles, and/or upper surfaces of the feet. It is nearly always bilateral. Characteristics include:

How is livedoid vasculopathy diagnosed?

After taking a history, the patient should undergo thorough general examination to identify any underlying associated condition.

Livedoid vasculopathy is a clinical diagnosis, supported by skin biopsy of a red papule or the edge of a new ulcer. Histopathology reveals hyalinisation, thickened blood vessel walls, fibrin deposition, vascular occlusion by thrombosis and minimal inflammation.

Direct immunofluorescence often shows deposition of immunoglobulin and complement components in the superficial, mid-dermal, and deep dermal vasculature (non-diagnostic).

Investigations are not diagnostic for livedoid vasculopathy. They should include:

In many cases of livedoid vasculopathy, the results of these tests are normal.

Imaging studies for peripheral vascular disease may be carried out. Transcutaneous oximetry shows reduced oxygen flow in most patients.

Differential diagnosis includes ulceration and atrophie blanche arising in other diseases:

What is the treatment for livedoid vasculopathy?

The main goal of therapy in livedoid vasculopathy is to reduce pain, ulceration and the development of atrophie blanche.

Various drug therapies may be prescribed to enhance blood flow and/or prevent blood clotting:

What is the outlook for livedoid vasculopathy?

Livedoid vasculopathy is a chronic disorder, with spontaneous remissions and exacerbations. Reports of disease duration have ranged from 2.5 months to 21 years.

Once livedoid vasculopathy is in remission, over time the white patches of atrophie blanche become less defined and capillaries less prominent.

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