Scleroderma treatment options in adults
Scleroderma, also known as systemic sclerosis, is a complex autoimmune disease characterized by the hardening and tightening of the skin and connective tissues. It can also affect internal organs such as the lungs, heart, kidneys, and gastrointestinal tract, leading to significant health challenges. While there is currently no cure for scleroderma, various treatment options aim to manage symptoms, prevent complications, and improve the quality of life for adults living with the condition.
Treatment strategies are highly individualized, depending on the severity of the disease, the organs involved, and the specific symptoms presented. The primary goal is to suppress abnormal immune responses, reduce inflammation, and slow disease progression. Immunosuppressive medications are often central to this approach. Drugs such as methotrexate, mycophenolate mofetil, and cyclophosphamide have been used to control skin thickening and lung involvement, with cyclophosphamide showing particular promise in cases of interstitial lung disease, a common complication.
In addition to immunosuppressants, vasodilators play a critical role in managing circulatory issues associated with scleroderma. Raynaud’s phenomenon, a condition where blood flow to fingers and toes is reduced, can be severe in these patients. Medications like calcium channel blockers (e.g., nifedipine) help dilate blood vessels, reducing the frequency and severity of attacks. For more stubborn cases, other vasodilators such as prostacyclin analogs or phosphodiesterase-5 inhibitors may be prescribed.
Skin fibrosis, a hallmark of scleroderma, can be addressed with medications like methotrexate or immunomodulators, which may slow skin thickening. Physical therapy and occupational therapy are also essential to maintain mobility, reduce stiffness, and prevent defor

mities. Regular skin care, including moisturization and protection from cold, helps alleviate discomfort and prevent skin damage.
Organ-specific treatments are vital as well. Pulmonary hypertension, a serious complication characterized by increased blood pressure in the lungs, may be treated with drugs like endothelin receptor antagonists or prostacyclins. Kidney involvement often requires careful blood pressure management, sometimes with ACE inhibitors, which can also protect kidney function. Gastrointestinal symptoms, such as acid reflux or motility issues, are managed with proton pump inhibitors, prokinetic agents, or dietary modifications.
Emerging therapies and clinical trials continue to offer hope. Biological agents that target specific immune pathways, such as rituximab or tocilizumab, are being studied for their potential benefits in scleroderma. Furthermore, lifestyle modifications, including smoking cessation, regular exercise, and stress management, contribute significantly to overall health and symptom control.
While managing scleroderma can be complex, a multidisciplinary approach involving rheumatologists, pulmonologists, nephrologists, and other specialists can optimize care. Early diagnosis and tailored treatment plans are crucial to prevent severe complications and enhance the patient’s quality of life. Although research is ongoing, current treatments focus on controlling symptoms, preventing organ damage, and supporting the body’s resilience against disease progression.









