Subacute cutaneous lupus (SCLE) is an autoimmune disease that affects the skin of your neck, shoulders, arms, back or chest. It causes red, ring-shaped sores and rashes that don’t itch or scar but may leave skin discoloration once they clear up. There’s no cure for SCLE, but treatment can help you manage symptoms and avoid flare-ups.
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Subacute cutaneous lupus erythematosus (SCLE) is one form of cutaneous lupus erythematosus (CLE), which is a type of lupus that affects your skin. People with SCLE develop red, ring-shaped or raised lesions on their neck, shoulders, arms, back or chest. “Subacute” refers to the depth of inflammation seen with a skin biopsy. About half of people with subacute cutaneous lupus also have the more common form of lupus, systemic lupus erythematosus (SLE).
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Subacute cutaneous lupus can be tricky to understand. Like other forms of lupus, it can look and act differently for everyone who has it. That can make it hard to diagnose. Look for a healthcare provider who will listen to your concerns and help you find treatment to manage the condition. It may also be helpful to look for support groups in your area or online. By listening to the experiences of others with the condition, you may feel more empowered to manage the disease.
The subtypes of SCLE include:
Subacute cutaneous lupus causes a rash. The rash typically occurs on sun-exposed areas of your body, like your neck, chest, back and arms. The rash can look like:
The rash typically doesn’t itch or scar. But when the rash resolves, it may leave skin discoloration.
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The cause of SCLE is complex. Researchers believe it likely involves genetic factors as well as environmental factors like ultraviolet radiation, medications, tobacco use and pesticides.
In about one-third of people with SCLE, the condition develops after taking certain medications like:
Lupus has a strong genetic component, meaning it runs in families. Subacute cutaneous lupus is also more common in:
Because people with subacute cutaneous lupus have to protect themselves from the sun so much, they may end up developing a vitamin D deficiency. In addition, the condition can lead to extreme discomfort and may affect your quality of life.
A dermatologist (a doctor specializing in skin, hair and nails) or a rheumatologist (a doctor specializing in arthritis) can diagnose subacute cutaneous lupus. Your provider will perform a physical examination and ask you about your symptoms. In addition, they may request a skin biopsy. During a biopsy, your provider removes a small sample of skin. The skin is sent to a laboratory to be examined under a microscope. This examination can determine whether a skin rash is due to lupus or another condition.
If your healthcare provider suspects SCLE, they may request additional tests to confirm their diagnosis. These tests may include:
The most important treatment for SCLE is sun protection. Make sure to apply a broad-spectrum sunscreen of SPF 50 or higher when you’re out in the sun.
Depending on how severe your symptoms are, your healthcare provider may recommend topical or oral medications.
Treatments may include:
You can’t prevent subacute cutaneous lupus. To decrease the frequency and severity of skin rashes:
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Certain triggers typically cause SCLE rash flares. Most commonly, lupus flares occur after exposure to ultraviolet (UV) light.
To protect yourself from UV exposure:
Subacute cutaneous lupus is a lifelong (chronic) condition that waxes and wanes. You’ll have to work with your healthcare provider to determine which treatment options help relieve your symptoms. It’s also important to protect yourself from the sun to avoid symptom flare-ups.
Learning to live with subacute cutaneous lupus can be challenging. Your life has changed, but there are ways to help you live with the disease and put you in control.
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See your healthcare provider if you develop any symptoms of subacute cutaneous lupus. They may refer you to a dermatologist to make a diagnosis. It’s important to find a provider that you trust. Someone who will take the time to listen to your concerns and work with you to find medications that will help relieve your symptoms. You may need to see them regularly as symptoms can change, and you also may need adjustments to your medications over your lifetime.
You may want to ask your provider:
Getting a subacute cutaneous lupus diagnosis can be difficult. You probably have lots of questions racing through your head, from what caused this to what this means for your future. The answers aren’t always clear, and it can feel scary and overwhelming. But know that you’re not alone.
The lupus community has many resources to help guide you as you learn to live with the condition. Work with a trusted healthcare provider to find the right treatment for you. Ask them to point you toward support groups or therapists in your area that can help you feel more in control of your condition. Take a deep breath. You’ve got this.
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Last reviewed on 10/25/2024.
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