Lipoedema

Signs and symptoms

In lipoedema, the legs become enlarged from the ankles up to the hips.Both legs are usually enlargedat the same time and to the same extent.

The feet are not affected and this creates a bracelet effect or band-like appearance just above the ankles.

The hands are not usually affected either, although the arms occasionally canbe.

The degree of enlargement caused by lipoedema differs between individuals with the conditionand it can gradually worsen over time.

As well as becoming enlarged, affected areas of the body may:

feel soft, 'doughy' and cold
be tender to touch
bruise easily
ache or feel painful
have small broken veins under the skin

The condition can progress to cause fluid retention ( Lymphoedema ) in the affected legs.

The combination of these symptoms can lead to reduced mobility and psychological issues, such as low self-esteem.

Medically Reviewed by a doctor on 21 Dec 2018

Articles for lipoedema

Introduction

Lipoedema is a poorly understood long-term (chronic) condition typically involving an abnormal build-up of fat cells in the legs, thighs and buttocks.

Signs and symptoms

In lipoedema, the legs become enlarged from the ankles up to the hips.Both legs are usually enlargedat the same time and to the same extent. The feet are not affected and this creates a bracelet ef

What causes lipoedema?

The cause of lipoedema is not known, but there is a family history of the conditioninsome cases and it seems likely that the genes you inherit from your parentsplaya role. Lipoedema tends to start at

Seeking medical advice

You should see your GP if you have symptoms of lipoedema so they can try to identify the cause. This will usually involve examining the affected areas of your body to help determine whether you have

Treating lipoedema

As there has been little research into lipoedema, there is some uncertainty about the best way to treat the condition. Generally, the main treatment optionsare non-surgical treatments and liposuction

Information about you

If you have lipoedema, your clinical team may pass information about you on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS). This helps scientists look for better

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