Scleroderma is a chronic disease that causes abnormal growth of connective tissue. It can affect the joints, skin, and internal organs. It is degenerative and gets worse over time. The disease can be in one area of the body. This is known as localized scleroderma. Or it may affect the whole body. This is known as systemic sclerosis. Scleroderma is more common in women.
Scleroderma is thought to be an autoimmune disease. This means the symptoms are caused by the body attacking its own healthy tissues. Genes play a role in the disease, but the environment also plays a role. Family members of people with scleroderma have a mildly increased risk of developing scleroderma. But many people with scleroderma don't have family members with the condition.
Scleroderma can lead to scarring of the skin, joints, and internal organs. Symptoms can occur a bit differently in each person, and may include:
Calcium bumps on the fingers or other bony areas
Grating noise as inflamed tissues move
Heart failure and abnormal heart rhythms
Immovable fingers, wrists, or elbows because of scarring of the skin
Pale and tingly fingers that may turn numb when exposed to cold or during emotional upset (Raynaud’s phenomenon)
Scarring of the esophagus. This leads to heartburn and trouble swallowing.
Scarring of the lungs. This leads to shortness of breath.
Sores on fingertips and knuckles
Tight, shiny, darker skin on large areas that may cause problems with movement
Thickening and swelling of the tips of the fingers
The symptoms of scleroderma can look like other health conditions. Make sure to see your healthcare provider for a diagnosis.
The process starts with a health history and a physical exam. Diagnosis is based on the changes in the skin and internal organs. An antibody test may help show the type of scleroderma. You may need tests such as:
Electrocardiogram (ECG). This test records the electrical activity of the heart, shows abnormal rhythms, and detects heart muscle damage. An ECG may be done to find changes in the heart muscle tissue caused by scleroderma.
Echocardiogram. This test uses sound waves to create a moving image of the heart and its valves. It is done to look at the structure and function of the heart.
X-ray. This test uses a small amount of radiation to create images of internal tissues, bones, and organs. X-rays may show changes in bone, soft tissues, and organs caused by scleroderma.
CT scan. A chest CT scan uses X-rays and a computer to make images of the body. It may be done to check for intersitial lung disease and bone abnormalities.
Treatment will depend on your symptoms, age, and general health. Treatment may include:
Nonsteroidal anti-inflammatory medicines or corticosteroids to relieve pain
Penicillamine to slow the skin thickening process and delay damage to internal organs
Immunosuppressive medicines, such as methotrexate
Treatment of specific symptoms, such as heartburn and Raynaud’s phenomenon
Physical therapy and exercise to maintain muscle strength
Talk with your healthcare providers about the risks, benefits, and possible side effects of all medicines.
With localized scleroderma, some symptoms may get better over time. But damage to skin and other organs may be permanent. With systemic sclerosis, symptoms can over time lead to damage to the skin and cause thickened, tight skin. This can change your appearance. And it can cause problems with your movement. It can also cause severe kidney, lung, digestive, or heart problems. In some cases, these organ problems can lead to death.
Systemic scleroderma is a long-term (chronic) condition. It is important that you learn ways to best manage your symptoms. Learn about the disease and work with healthcare providers who have experience with scleroderma. Because scleroderma can affect so many systems of the body, you may need to have many specialists on your health team. Physical and occupational therapists may help you with managing your activities of daily living. Make sure that you and other team members are in regular touch with each other. If you are not able to manage your care, pick a trusted person to oversee your care. Make sure to address your emotional well-being, too. Don't hesitate to ask for help when you need it.
If your symptoms get worse or you have new symptoms, let your healthcare provider know.
Scleroderma causes abnormal growth of connective tissue. It can affect the joints, skin, and internal organs.
Scleroderma can affect one area of the body, or affect the whole body.
There is no cure for scleroderma. Treatment is focused on easing pain and slowing down damage to the body.
Tips to help you get the most from a visit to your healthcare provider:
Know the reason for your visit and what you want to happen.
Before your visit, write down questions you want answered.
Bring someone with you to help you ask questions and remember what your healthcare provider tells you.
At the visit, write down the name of a new diagnosis, and any new medicines, treatments, or tests. Also write down any new instructions your provider gives you.
Know why a new medicine or treatment is prescribed, and how it will help you. Also know what the side effects are.
Ask if your condition can be treated in other ways.
Know why a test or procedure is recommended and what the results could mean.
Know what to expect if you do not take the medicine or have the test or procedure.
If you have a follow-up appointment, write down the date, time, and purpose for that visit.
Know how you can contact your healthcare provider if you have questions.