How long can you live with diffuse scleroderma?

How long can you live with diffuse scleroderma?

Patients with diffuse cutaneous systemic sclerosis have a 10-year survival estimate of approximately 75%. However, development of ILD, PAH, or renal crisis dramatically increases the risk of death.

How fast can scleroderma progress?

About 50 percent of patients have a slower and more benign illness called limited scleroderma. In limited scleroderma, skin thickening is less widespread, typically confined to the fingers, hands and face, and develops slowly over years.

Can you live a full life with diffuse scleroderma?

Many people have a good scleroderma prognosis – they do not die of the disease and live a full and productive life. However, some people do die from scleroderma, for example those with severe lung, heart or kidney involvement.

Is limited scleroderma progressive?

Limited scleroderma is a chronic but slowly progressive condition. Importantly, patients usually do not usually expire from the disease.

What causes progressive systemic scleroderma?

Causes of Systemic Sclerosis SS occurs when your body begins to overproduce collagen and it accumulates in your tissues. Collagen is the main structural protein that makes up all of your tissues. Doctors aren’t sure what causes the body to produce too much collagen. The exact cause of SS is unknown.

What is the life expectancy of a person with scleroderma?

Females were overrepresented 315 to 98; 265 had limited scleroderma, 90 diffuse and 22 overlap disease. Over 30 years, the mean age of death improved from 66.4 to 74.5 years (P < 0.001). Duration of disease improved from 12.1 to 22.9 years (P < 0.001).

What is the prognosis for scleroderma?

There is no cure for scleroderma, but you can reduce damage from the disease with proper treatment. Since some types of scleroderma can cause serious damage to your internal organs, it is important to monitor your health and let your doctor know if you notice any new symptoms.

Can you die from systemic scleroderma?

Patients with limited cutaneous scleroderma have a 10-year survival rate of 75%; less than 10% develop pulmonary arterial hypertension after 10 to 20 years. Patients with diffuse cutaneous scleroderma have a 10-year survival rate of 55%. Death is most often caused by lung, heart, and kidney involvement.

What is progressive systemic sclerosis?

Progressive systemic sclerosis (SSc), also known as scleroderma, is a connective tissue disease. Symptoms of SSc are: thickening and hardening of the skin and internal organs, abnormalities of the immune system. The most common symptom of this disease is a color change in your hands and feet when they are exposed to the cold.

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