Scleroderma is a rare disease of the connective tissue. It can cause the tissue in skin, joints, and internal organs to thicken and stiffen. There are 3 major forms of the disease: Localized scleroderma—Usually affects only the skin in isolated parts of the body. This form is less serious. Morphea—local patches of sclerodermaLinear scleroderma—single line or band of thickened or abnormally colored skin.Systemic scleroderma (sclerosis)—Affects widespread areas of skin and/or internal organs, most often the lungs. Also involves Raynaud phenomenon. Certain categories of this form of scleroderma are more serious and can be fatal. Limited A gradually progressing form of scleroderma that initially causes skin thickening, most commonly on the hands, forearms, feet, and lower legsUsually progresses to affect the internal organs.Diffuse A more quickly progressing form of scleroderma that causes the skin to thicken throughout the body.It may also affect the internal organs.Sclerosis sine scleroderma—very rare form of scleroderma in which there are no skin manifestations, but the internal organs are affected. Overlap syndrome—May involve features of scleroderma and features of other autoimmune syndromesUndifferentiated scleroderma—Involves Raynaud phenomenon and a few aditional features of systemic sclerosis.
Overproduction of collagen and other connective tissue proteins are the main features of scleroderma. It is not clear what causes this overproduction. Malfunction of the immune system may contribute to excess collagen production.
Scleroderma is more common in women. The morphea type of scleroderma usually affects people 20-40 years old. Linear scleroderma often occurs in children. Systemic scleroderma is more likely to occur in people aged 30-50 years old.
Other factors that may increase your risk of developing scleroderma include: Family members with systemic sclerosis or other autoimmune disorders, such as systemic lupus erythematosusOccupational chemical exposure, such as silica, ketones, or welding fumes
Symptoms are usually restricted to the skin. This disorder does not progress to involve internal organs. The skin lesions may completely reverse themselves in a few months or a few years. In some cases, they lead to permanent disfigurement. Symptoms include: Hard patches on the skin, most often on the face or trunk (morphea)Lines of plaques or thickened skin. Thickening can extend to underlying muscles and bones (linear scleroderma or linear morphea)Muscle and joint aches, and tiredness may occur with morphea
This form of the disease is typically categorized as either limited or diffuse disease. Many cases of limited disease begin gradually with
Raynaud's phenomenon. This involves swelling, tingling, numbness, blue and white color, and pain in fingers and toes. The fingers turn red after resolution of the symptoms. It is brought on by cold or emotional distress. The condition can progress over the years to thickened skin.
Raynaud's Phenomenon Symptom
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Diffuse scleroderma comes on more suddenly and can progress to involve not only the skin but the internal organs. Other symptoms of diffuse scleroderma may include: Diffuse thickening and hardening of the skinJoint and muscular pain, stiffness, and swellingProblems with breathing, swallowing, and digesting food due to thickening and hardening of lung, esophagus, bowel tissuesInflammation and thickening of large and small blood vessels
Complications of diffuse scleroderma can affect virtually every system of the body. Other common complications include: Skin ulcersBleedingInterstitial lung diseasePulmonary hypertensionHeart rhythm problemsHeart failureKidney failureHigh blood pressure
You will be asked about your symptoms and medical history. A physical exam will be done. Diagnosis is based on changes in the skin.
Tests may include: Blood tests—results may be typical of scleroderma, but do not prove itBiopsies
of skin and other tissues
Imaging tests take pictures of internal body structures. These may include: X-rayMRICT scan
In addition, an esophagus motility study may be done
There is no treatment to cure scleroderma. Treatments are aimed at relieving symptoms in various systems.
Nonsteroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen and naproxenCorticosteroids
Medications to limit acid production in the stomachSmall, frequent meals
Sleeping with your head elevated to avoid
acid reflux CorticosteroidsImmunosuppressantsProstanoids—drugs that control the immune systemPhototherapy
ACE inhibitors, or other antihypertensive drugsAntineoplastic agentsVasodilators
Calcium channel blockersProper shelter and clothing to avoid coldProstanoids—drugs that control the immune system
If you smoke, talk to your doctor about ways to quit.
There are no current guidelines to prevent scleroderma.
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Mathai SC, Girgis RE, et al. Addition of sildenafil to bosentan monotherapy in pulmonary arterial hypertension.
Eur Respir J. 2007;29:469-475.
Rodriguez-Reyna TS, Alarcon-Segovia D. Overlap syndromes in the context of shared autoimmunity.
Scleroderma. National Institute of Arthritis and Musculoskeletal and Skin Diseases website. Available at:
http://www.niams.nih.gov/Health_Info/Scleroderma/default.asp. Updated August 2016. Accessed November 29, 2016.
What is scleroderma? Scleroderma Foundation website. Available at:
Accessed November 29, 2016.
11/9/2015 DynaMed's Systematic Literature Surveillance http://www.ebscohost.com/dynamed: 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.
Last reviewed February 2016 by Michael Woods, MD
Please be aware that this information is provided to supplement the care provided by your physician. It is neither intended nor implied to be a substitute for professional medical advice. CALL YOUR HEALTHCARE PROVIDER IMMEDIATELY IF YOU THINK YOU MAY HAVE A MEDICAL EMERGENCY. Always seek the advice of your physician or other qualified health provider prior to starting any new treatment or with any questions you may have regarding a medical condition.
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