Scleroderma is a lifelong disease. It causes damage to the structures that support and protect the body. It can cause skin and other structures to thicken and stiffen. This can happen in the skin, joints, and internal organs.
There are 3 types:
Localized—Involves the skin and other parts. The areas are not near each other.
- Morphea—Made up of local patches.
- Linear—Single line or band of skin that's thickened or discolored
Systemic (sclerosis)—Over a wider area of skin and organs (mainly the lungs). This type is more serious and can lead to death.
(RP) is related to this type.
Limited—Sometimes called CREST syndrome:
- Skin thickening happens slowly. This happens mostly on the hands, forearms, feet, and lower legs.
- May progress to the organs.
- Happens quicker. It causes the skin to thicken throughout the body.
- May progress to the organs.
- Sclerosis sine scleroderma—Involves the organs, not the skin. This type is very rare.
- Limited—Sometimes called CREST syndrome:
- Overlap syndrome—May involve features of scleroderma and other connective tissue syndromes.
- Undifferentiated—Involves RP and some features of the systemic type.
Problems are contained to the skin. It doesn’t involve the organs. The skin problems may go away on their own. It may take a few months or years. For some, damage can be permanent. Skin problems may involve:
- Hard patches on the skin, most often on the face or trunk—morphea
- Lines of plaques or thickened skin
- May spread to muscles or bones under the skin—linear
- Muscle and joint aches, and fatigue—morphea
Systemic disease may be limited or diffuse. The limited type can start slowly. Most often, it involves RP. Cold or emotional stress cause swelling, numbness, and color changes in the fingers and toes. Over time, the skin may thicken.
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The diffuse type comes on faster. It spreads to the skin and organs. Other problems of this type:
- The skin thickens and gets harder
- Joint and muscle pain—there may also be stiffness and swelling
- Breathing problems
- Swallowing problems
- Blood vessels thicken and swell
The diffuse type can cause problems all over the body. This may involve:
- Skin sores
- Interstitial lung disease
- Pulmonary hypertension
- Heart rhythm problems
- Heart failure
- Kidney failure
- High blood pressure
There is no cure for scleroderma. Care focuses on easing symptoms.
Your doctor may advise these or other medicines to treat:
- Pain and swelling
- The immune system
- Gastroesophageal reflux disease —GERD
- High blood pressure
- Narrowed blood vessels
Other care may involve:
- Physical therapy and exercise to help with circulation, flexibility, and strength
- Phototherapy —to thin out the skin
- Changes to control GERD such as eating smaller meals or raising the head of your bed
- Quitting smoking to improve blood flow
This content is reviewed regularly and is updated when new and relevant evidence is made available. This information is neither intended nor implied to be a substitute for professional medical advice. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with questions regarding a medical condition.
Edits to original content made by Denver Health.
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a (Systemic Sclerosis)
Scleroderma Foundation http://www.scleroderma.org
Scleroderma Research Foundation http://www.srfcure.org
Arthritis Society http://www.arthritis.ca
Scleroderma Canada http://www.scleroderma.ca
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Scleroderma. National Institute of Arthritis and Musculoskeletal and Skin Diseases website. Available at: https://www.niams.nih.gov/health-topics/scleroderma. Accessed June 20, 2018.
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What is scleroderma? Scleroderma Foundation website. Available at: http://www.scleroderma.org/site/PageNavigator/patients%5Fwhatis.html#.Wy58BVVKhxA. Accessed June 20, 2018.
11/9/2015 DynaMed Plus Systematic Literature Surveillance http://www.dynamed.com/topics/dmp~AN~T116347/Systemic-sclerosis : Kuo CF, Grainge MJ, Valdes AM, et al. Familial aggregation of systemic lupus erythematosus and coaggregation of autoimmune diseases in affected families. JAMA Intern Med. 2015;175(9):1518-1526.