URL of this page: http://www.nlm.nih.gov/medlineplus/ency/article/000429.htm
Alternative names
CREST syndrome; Progressive systemic sclerosis; SclerodermaDefinition
Scleroderma is a diffuse connective tissue disease characterized by changes in the skin, blood vessels, skeletal muscles, and internal organs.Causes, incidence, and risk factors
The cause of scleroderma is unknown. The disease may produce local or systemic symptoms. The course and severity of the disease varies widely in those affected.
Excess collagen deposits in the skin and other organs produce the symptoms. Damage to small blood vessels within the skin and affected organs also occurs. In the skin, ulceration, calcification, and changes in pigmentation may occur.
Systemic features may include fibrosis and degeneration of the heart, lungs, kidneys and gastrointestinal tract.
The disease usually affects people 30 to 50 years old. Women are affected more often than men. Risk factors are occupational exposure to silica dust and polyvinyl chloride.
Symptoms
Signs and tests
Examination of the skin may show tightness, thickening, and hardening.Treatment
See scleroderma treatment.Support Groups
See scleroderma - support group.Expectations (prognosis)
In the majority of those affected, the disease is progressive. In some, remission occurs with a slow progression. People who only have skin involvement have a better prognosis (probable outcome). Death may occur from gastrointestinal, cardiac, kidney, or pulmonary (lung) involvement.Complications
Calling your health care provider
Call for an appointment with your health care provider if symptoms of this disorder are present, or if you have scleroderma and symptoms become worse, or if new symptoms develop.Prevention
There is no known prevention. Minimize exposure to silica dust and polyvinyl chloride. Update Date: 8/6/2003 Updated by: Megan E. B. Clowse, M.D., M.P.H., Division of Rheumatology, Johns Hopkins Hospital, Baltimore, MD. Review provided by VeriMed Healthcare Network.