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Livedo Reticularis – Types, Symptoms, and Complications

Definition

Livedo reticularis (LR) is a common vascular reaction pattern characterized by a reticular (net-like) discoloration on the extremities and trunk. It is caused by decreased blood flow to the skin or impaired outflow in the dermal venous plexus and stagnation of the blood within these vessels. The darker, discolored areas represent the accumulation of deoxygenated blood. Etiologic categories include vasospasm, vessel wall dysfunction (e.g., vasculitis), and vascular flow compromise as in coagulopathies.

LR is exacerbated by cold temperatures. It may be physiologic (cutis marmorata), a primary disease (as in idiopathic cases), or it may be secondary to underlying disorders such as antiphospholipid antibody syndrome, vasculopathy, or autoimmune connective tissue disorders. Amantadine, quinidine, and catecholamines have also been described as triggers. Drugs used in the past to treat syphilis (bismuth and arsphenamine) also caused LR. Furthermore, infections can induce LR via the formation of cryoglobulins, cold agglutinins, septic emboli, immune vasculitis, or septic vasculitis. In adults, LR is frequently seen in patients with the Raynaud phenomenon, in those with a predisposition to chilblains and acrocyanosis, and in patients with poor vascular flow (eg, peripheral vascular disease and cardiac failure).

These secondary forms may also present with livedo racemosa, where the reticular pattern is asymmetric, discontinuous, and localized. Localized forms may be associated with vasculitis. In severe cases, the extremities are cold and ulcers may form. Sneddon syndrome is extensive diffuse LR or livedo racemosa with cerebrovascular disease (from transient ischemic attacks to frank cerebrovascular accidents), hypertension, and antiphospholipid antibodies.

Types of Livedo reticularis

Based on the duration of the livedo, called the violet discoloration pattern, and the temperature, the livedo reticularis is divided into four types. The four types of LR are physiologic livedo reticularis, primary livedo reticularis, Idiopathic livedo reticularis, Amantadine induced livedo reticularis.

Physiologic Livedo Reticularis: also known as cutis marmorata. This type of livedo reticularis occurs due to exposure to cold temperatures; blood supply is disturbed by the excess cold temperature resulting in cyanotic discoloration of the skin. The symptoms will get resolved with an increase in temperature. Young women are mostly affected by physiologic livedo reticularis. The most commonly affected area is the leg.

Primary Livedo Reticularis: It is a benign form of LR with discoloration of the skin with unknown cause. Idiopathic livedo reticularis is the early stage of Sneddon syndrome, antiphospholipid syndrome, or APS. Amantadine-induced livedo reticularis: livedo reticularis is caused by amantadine. The catecholamines provoke arteriolar vasospasm.

Other varieties of include:

Cutis Marmorata Telangiectatica Congenita or CMTC: It is the congenital form of livedo reticularis. Features are persistent.

Livedo Racemosa: It is a persistent and generalized variety of livedo reticularis.

Secondary Livedo Reticularis: Livedo reticularis is caused due to underlying systemic diseases.

Epidemiology

LRC is the most common dermatologic presentation in patients with antiphospholipid syndrome (APS), presenting in 25% of patients with primary APS and in 70% of patients with SLE-associated APS.

Causes of Livedo reticularis

Generally, it arises from altered blood flow in the skin microcirculation (the small blood vessels that supply the skin). A variety of factors reduce the flow of fresh arterial blood to the skin. This leads to the collection of venous blood and gives rise to the typical purplish color.

Cold weather can induce the arteriolar walls to spasm. However, in physiologic livedo reticularis, the pattern tends to disappear when the affected area is warmed.

Other causes include reduced blood flow due to hyperviscosity (thickened consistency of the blood), vessel wall pathology (e.g., from blood vessel inflammation), or obstruction (e.g., from a blood clot inside the vessel).

Symptoms

Common symptoms are:

Symptoms of LR

Complications

LR itself is relatively benign. However, thromboembolic disease due to associated conditions such as antiphospholipid syndrome may lead to serious arterial events, including the death of the patient.

Livedo reticularis risk factors

LR is harmless. But some conditions can cause it to happen more often. Some conditions that make livedo reticularis more likely include:

‌These conditions often affect your nervous and vascular systems. This might be why they’re connected to cutis marmorata. Your nervous system might be less prepared to react to the cold. This causes your skin to marble.

Treatment

The best therapy for you depends on the type:

Diagnosis

Given the characteristic appearance of this disorder and the typical circumstances in which it arises, the diagnosis of LR is typically simple. Most of the cases, LR is a common occurrence, requiring no further examination.

LR Differential Diagnosis

If the circumstances surrounding the skin coloring or how it appears to suggest a pathological origin, the diagnosis may become difficult. In these situations, the doctor will start by taking a thorough medical history and physical examination.

Targeted diagnostic testing may be done to look for the suspected underlying condition.

If the initial evaluation does not point in a particular direction, the doctor may also order:

Prevention of Livedo reticularis

Mottled skin can vary in its ability to be prevented depending on what is causing it. However, adopting measures to stay warm and increase blood flow may be beneficial if someone has cutis marmorata or another condition that affects body temperature or circulation.

Anybody can try:

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