Scleroderma Specialists in Bogadi, Mandya, Karnataka

Scleroderma is a chronic autoimmune disease that causes the body to produce excess collagen, leading to hardening and tightening of the skin and, in more severe…

What is Scleroderma?

Scleroderma is a chronic autoimmune disease that causes the body to produce excess collagen, leading to hardening and tightening of the skin and, in more severe forms, internal organs such as the lungs, heart, kidneys, and digestive tract. It ranges from localized forms that primarily affect the skin to systemic sclerosis, which can be life-threatening due to organ involvement. The condition is more common in women and typically develops between ages 30 and 50. Its course and severity vary considerably between individuals.

Severity

Severe

Prevalence

Rare — affects about 50-300 per million people

Contagious

Causes of Scleroderma

Caused by an autoimmune process that triggers overproduction of collagen, though the exact trigger remains unknown. Genetic susceptibility combined with environmental exposures such as certain chemicals or silica dust is thought to play a role, and abnormal blood vessel function contributes to symptoms like Raynaud's phenomenon.

Symptoms of Scleroderma

Thickened and hardened patches of skin, Raynaud's phenomenon with fingers turning white or blue in cold, joint pain and stiffness, difficulty swallowing, shortness of breath, digestive problems like acid reflux, fatigue, skin tightness around the mouth and fingers, calcium deposits under the skin

Treatment & Types of Scleroderma in Bogadi, Mandya, Karnataka

There is no cure, so treatment focuses on managing symptoms and preventing organ complications using medications to control blood pressure, improve blood flow, and suppress the immune response as needed. Physical therapy helps maintain skin and joint flexibility, and regular monitoring for lung, heart, and kidney involvement is essential for early intervention.

Scleroderma has two main forms: localized scleroderma, which affects only the skin and underlying tissue in patches without involving internal organs, and systemic sclerosis, which can affect internal organs such as the lungs, heart, kidneys, and digestive tract in addition to the skin. Systemic sclerosis is further divided into limited cutaneous, where skin thickening is confined mainly to the hands, forearms, and face with a generally slower course, and diffuse cutaneous, where skin thickening spreads more widely and organ involvement tends to progress faster.

Rheumatology Specialists in Bogadi, Mandya, Karnataka (0)

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Frequently Asked Questions

Is localized scleroderma as serious as systemic sclerosis?

No, localized scleroderma affects only the skin and underlying tissue without involving internal organs, making it generally much less serious than systemic sclerosis, which can affect the lungs, heart, and kidneys and requires closer monitoring. This distinction is one of the first things a rheumatologist establishes after diagnosis.

Can scleroderma be cured?

There is no cure, so treatment focuses on managing symptoms and preventing organ complications through medications that control blood pressure, improve blood flow, and suppress the immune response as needed. Regular monitoring for lung, heart, and kidney involvement allows early intervention if complications develop.

What is Raynaud's phenomenon and why does it happen with scleroderma?

Raynaud's phenomenon causes fingers to turn white or blue in response to cold due to abnormal blood vessel function, a common early symptom that reflects the same underlying blood vessel abnormality seen throughout scleroderma. Protecting the hands from cold exposure and avoiding smoking help manage this symptom.

Is scleroderma hereditary?

Genetic susceptibility does play a role, but scleroderma is not typically considered a straightforwardly inherited disease; environmental exposures such as certain chemicals or silica dust are thought to interact with genetic factors to trigger the autoimmune process. Having a family member with scleroderma or another autoimmune disease is a relevant but not definitive risk factor.

What organ complications need monitoring in systemic sclerosis?

Regular monitoring focuses on the lungs, heart, and kidneys since involvement of these organs drives most of the serious long-term risk, and catching early changes allows treatment to start before significant damage occurs. A rheumatologist typically coordinates this monitoring alongside specialists for each affected organ system.

Learn more about Scleroderma (symptoms, causes, treatment)

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