Skin

Difference Between Scleroderma and CREST

Difference Between Scleroderma and CREST

Limited scleroderma, also known as CREST syndrome, is one subtype of scleroderma — a condition whose name means "hardened skin." The skin changes associated with limited scleroderma typically occur only in the lower arms and legs, below the elbows and knees, and sometimes affect the face and neck.

  1. What are the symptoms of Crest?
  2. How serious is Crest syndrome?
  3. How long can you live with Crest syndrome?
  4. What does scleroderma skin look like?
  5. Is Crest syndrome a rare disease?
  6. Where does scleroderma usually start?
  7. What is the treatment for Crest syndrome?
  8. Is Crest syndrome a disability?
  9. How quickly does scleroderma progress?
  10. What is the best treatment for scleroderma?
  11. What vitamins are good for scleroderma?
  12. Is Turmeric Good for scleroderma?

What are the symptoms of Crest?

CREST Syndrome and Scleroderma

How serious is Crest syndrome?

CREST Syndrome and Pulmonary Hypertension

CREST syndrome coupled with pulmonary hypertension (elevated blood pressures within the lungs) can lead to heart and respiratory failure. See your doctor for advanced, integrated diagnosis and treatment.

How long can you live with Crest syndrome?

In a large 2003 US study by Mayes et al, the survival rate from time of diagnosis was computed to be 77.9% at 5 years, 55.1% at 10 years, 37.4% at 15 years, and 26.8% at 20 years. The extent of skin involvement is a good predictor of survival in patients with scleroderma.

What does scleroderma skin look like?

These patches may be shaped like ovals or straight lines, or cover wide areas of the trunk and limbs. The number, location and size of the patches vary by type of scleroderma. Skin can appear shiny because it's so tight, and movement of the affected area may be restricted. Fingers or toes.

Is Crest syndrome a rare disease?

Scleroderma is a rare disease, affecting an estimated 300,000 Americans—less than . 1% of the country's population. CREST Syndrome, a subcategory of the disease, is rarer still.

Where does scleroderma usually start?

Morphea usually appears between the ages of 20 and 50, but is often seen in young children. Linear scleroderma is a form of localized scleroderma which frequently starts as a streak or line of hardened, waxy skin on an arm or leg or on the forehead.

What is the treatment for Crest syndrome?

Simple surgical management, including curettage, is often sufficient in limited disease. Treatment with oral corticosteroids is not usually considered effective, but, according to Hazen et al, intralesional corticosteroid therapy has been associated with improvement of calcinosis.

Is Crest syndrome a disability?

If you suffer from CREST syndrome and are no longer able to work because of the effects of your symptoms on your daily functioning, you may be eligible to receive Social Security disability benefits, either through SSDI or SSI.

How quickly does scleroderma progress?

In the diffuse form of the disease, skin symptoms tend to peak within three years, then stabilize or even improve. If skin changes occur more rapidly, there is often a greater risk that internal organs are being damaged as well.

What is the best treatment for scleroderma?

Scleroderma Treatment

What vitamins are good for scleroderma?

Consider taking an over the counter multivitamin/mineral supplement containing 15 mg zinc, 10-18 mg iron, vitamins A, D, E, and K, folate, and B-12. If specific nutrient deficiencies have been identified, extra supplementation may be required.

Is Turmeric Good for scleroderma?

Recent research shows that curcumin, a component of turmeric, may benefit people who suffer from scleroderma. Scleroderma is a disorder where the body produces excessive amounts of connective tissue called collagen. This fibrous tissue builds up in the skin and other organs and can disrupt their function.

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