Systemic sclerosis (scleroderma)
About Systemic sclerosis (scleroderma)
Systemic sclerosis (also called scleroderma) is a rare disease in which scar tissue deposits in the skin and many internal organs. Scleroderma can affect only the skin or involve other parts of the body. This disorder is thought to be an autoimmune disease. This means the immune system mistakenly attacks certain organs of the body. The disease can be serious leading not only to scarring of the skin but also to damage of the esophagus, heart, lungs and kidneys. Scleroderma is most frequently diagnosed in people between the ages of 30 and 50 and is more common among women.Symptoms
Color changes in the fingers after exposure to cold (Raynaudâs phenomenon), thickening of the skin, weakness, fatigue, joint pains, shortness of breath, kidney failure.Tests & Diagnostics
A history and physical exam will be performed. Blood tests and imaging tests (such as a chest x-ray or CT scan) may be performed to help establish the diagnosis.Common tests: ANA, Complete blood count (CBC), Comprehensive metabolic panel (CMP), Rhematoid factor, Urinalysis (UA), X-ray.
OTC sleep aids and supportive treatments
Prescription medications
Conventional treatment summary
The goals of treatment are to reduce symptoms and to prevent and treat complications. Medications to dilate (open up) blood vessels, lower blood pressure, reduce inflammation and suppress the immune system may be recommended. More aggressive treatments such as bone marrow transplantation are being studied.Medical specialties
Internal Medicine · Rheumatology · Family Practice · Pediatric Rheumatology
This page is educational content, not medical advice. Always consult a qualified clinician for diagnosis and treatment of Systemic sclerosis (scleroderma).