Health condition
Livedo reticularis vs livedo racemosa
Livedo is a net-like purple mottling of the skin: the regular, complete net of livedo reticularis is usually a harmless response to cold, whereas the broken, irregular net of livedo racemosa is fixed and signals underlying vascular disease.
Why trust this guide
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Editorial team
Written by our editorial team from the UK sources listed on each page.
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Sourced from guidance
Checked against current NHS and UK specialist society guidance at the time of review.
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Current for 2026
Reviewed on 2026-09-27 with the next review scheduled for 2027-09-27.
Key facts
The essentials at a glance.
The symptoms to recognise, when to seek help, which specialist to see, and what treatment usually involves.
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Livedo reticularis: a symmetrical, complete lace-like pattern that fades with warming - typically benign
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Livedo racemosa: an irregular, broken, lightning-bolt pattern that persists whatever the temperature
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Racemosa warrants investigation for antiphospholipid syndrome, vasculitis and Sneddon syndrome
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A deep wedge biopsy from the pale centre of the net - not the purple line - has the highest yield
Understanding the condition
What it is and what happens next.
What causes it, how it is diagnosed, and the treatment routes available in the UK.
What it is and how it feels
The mottled pattern arises when blood flow slows in the cone-shaped territories of skin supplied by individual small arteries: deoxygenated blood pools in the draining veins at the edges of each cone, drawing a purple net. In physiological livedo reticularis this is simply cold-induced vasospasm, common in young women and fully reversible with warmth.
Diagnosis and treatment routes
Livedo racemosa, by contrast, reflects genuine obstruction of dermal vessels, so the assessment includes antiphospholipid antibodies, autoimmune serology, cryoglobulins and a careful neurological history - the combination of racemosa and stroke defines Sneddon syndrome. Management is directed at the underlying cause, which may include anticoagulation when antiphospholipid syndrome is confirmed. In much of the UK, a routine NHS referral to the relevant specialist clinic can take several months, whereas an initial appointment with a private consultant is typically available within around two weeks.
Seeing a specialist
Who to see, and how quickly you can be seen.
The specialist for this condition is usually a consultant dermatologist. Your GP can refer you on the NHS, or you can arrange a private consultation directly.
A quiet reminder
This guide is for information, not medical advice.
Your GP knows your history and can tell you which parts apply to you. If in doubt, see them - and seek urgent care for any of the emergency symptoms described above.
Frequently asked
Common questions about Livedo reticularis vs livedo racemosa.
Quick, plain-English answers to what people ask us most.
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What is livedo reticularis?
Livedo reticularis is a lace-like, mottled purplish discolouration of the skin, usually on the legs, caused by changes in blood flow through small blood vessels. It's often harmless and can worsen with cold exposure, but can occasionally indicate an underlying condition.
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What is livedo racemosa, and how does it differ from livedo reticularis?
Livedo racemosa is a similar mottled skin pattern but with a more irregular, broken, net-like appearance compared to the more regular, complete rings of livedo reticularis. It's more often associated with an underlying medical condition, such as an autoimmune or clotting disorder, and warrants more thorough investigation.
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What causes livedo reticularis and racemosa?
Livedo reticularis is often simply related to cold sensitivity of blood vessels and can be entirely benign (physiological), while livedo racemosa is more frequently linked to underlying conditions such as antiphospholipid syndrome, vasculitis, or other clotting disorders. Identifying which pattern you have helps guide whether further investigation is needed.
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Is livedo reticularis or racemosa dangerous?
Livedo reticularis alone, especially if it improves with warming the skin, is usually benign, while livedo racemosa, particularly if persistent regardless of temperature, is more likely to signal an underlying condition needing investigation and treatment. A specialist assessment can clarify which pattern is present and what, if anything, needs further work-up.
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Is livedo reticularis or racemosa genetic?
Livedo reticularis itself isn't typically inherited, though some underlying conditions associated with livedo racemosa, such as certain autoimmune or clotting disorders, can have genetic risk factors. Individual assessment of any underlying cause would clarify any relevant genetic component.
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Can livedo reticularis or racemosa be treated?
Simple livedo reticularis often needs no specific treatment beyond keeping warm, as it tends to improve on its own with temperature change. Livedo racemosa requires treatment of any identified underlying condition, which can significantly improve the skin appearance alongside addressing the primary health issue.
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How are livedo reticularis and racemosa investigated?
Investigation typically involves assessing whether the pattern persists with warming (suggesting racemosa and an underlying cause) or improves (suggesting benign reticularis), along with blood tests for clotting or autoimmune conditions if racemosa or persistent symptoms are present. A dermatologist or rheumatologist can guide appropriate investigation.
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How can you tell the difference between livedo reticularis and racemosa by appearance alone?
Livedo reticularis typically forms complete, regular, ring-like patterns and improves with warming, while livedo racemosa forms broken, irregular patterns and persists regardless of temperature. This distinction, alongside further testing, helps determine whether investigation for an underlying cause is needed.
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Physiological (benign) vs pathological livedo — what's the difference?
Physiological livedo reticularis is a benign, cold-related skin change that improves with warming and needs no treatment, while pathological livedo, including racemosa, persists regardless of temperature and often signals an underlying medical condition requiring investigation and treatment. Persistence despite warming is a key clue prompting further assessment.
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When should I see a doctor about livedo skin changes, and how quickly can I be seen privately?
Persistent mottled skin discolouration that doesn't improve with warming should be assessed by a dermatologist or rheumatologist. Private specialist consultations can typically be arranged within about two weeks, considerably faster than standard NHS waiting times.