How do I recognize scleroderma?

How do I recognize scleroderma?

A rheumatologist recognizes systemic scleroderma based on typical symptoms such as circulatory disorders in the hands and changes in the skin. The autoantibodies can be detected with blood tests. If the antibody test is negative, there is probably no scleroderma.

Can you get old with scleroderma?

A total of 7080% of people with scleroderma are still alive 10 years after being diagnosed. And the survival time is getting longer. Life expectancy also depends on whether internal organs are affected.

Is Scleroderma Fatal?

The very rare disease scleroderma, also called systemic sclerosis, causes thickening and scarring of the connective tissue. Gradually, the lungs and other organs often also scar, which can be life-threatening for the patient.

Which doctor for scleroderma?

The rheumatologist is a specialist in diseases of joints, muscles and connective tissue. Because scleroderma can be characterized by increasing hardening of the connective tissue, the rheumatologist is often consulted by those affected. Rheumatologists also treat diseases of the immune system.

What can you do about scleroderma?

Further therapeutic measures are UV-A irradiation of the skin or lymphatic drainage. Physiotherapy and physiotherapy help to prevent the fingers from becoming stiff. Studies are currently still investigating whether a stem cell transplant is helpful. Often only short-term improvements are achieved.

What is systemic sclerosis?

Systemic sclerosis is a rare chronic disease of unknown cause characterized by diffuse fibrosis and vascular abnormalities in the skin, joints, and internal organs (particularly the esophagus, lower GI tract, lungs, heart, and kidneys).

Where does scleroderma come from?

Scleroderma (Greek “scleros” = hard; “derma” = skin) is a disease of the connective tissue system, in which the connective tissue is increased or hardened for reasons that have not yet been clarified.

What types of MS are there?

Examples of sclerosis are: amyotrophic lateral sclerosis, arteriosclerosis, multiple sclerosis, bone sclerosis, liver cirrhosis, lichen sclerosus, interstitial pulmonary fibrosis, melorheostosis.

What is Crest Syndrome?

The CREST syndrome is a special form of systemic sclerosis. The acronym stands for the main characteristics calcinosis, Raynaud’s syndrome, disturbed peristalsis in the esophagus (esophagus), sclerodactyly and telangiectasia.

Which antibodies in scleroderma?

Antibodies to DNA topoisomerase I (Scl-70) can be detected in approx. 20-40% in patients with diffuse systemic scleroderma and anti-centromere antibodies in 50-60% in patients with limited systemic sclerosis (CREST syndrome) will.

What is mixed collagen disease?

Mixed collagenosis (MCTD) is a rare collagenosis with a combination of the clinical symptoms of systemic lupus erythematosus (SLE), systemic sclerosis (SSc), polymyositis (PM) (see these terms) and / or rheumatoid arthritis (RA).

What is lupus erythematosus?

Systemic lupus erythematosus is a chronic autoimmune inflammatory disease of connective tissue that can affect joints, kidneys, skin, mucous membranes, and the walls of blood vessels.

How is lupus manifested?

Systemic lupus erythematosus usually starts with general and unspecific symptoms. Symptoms such as tiredness and fatigue, decreased performance, fever and weight loss are the most common. Lymph node swelling is also observed in about half of the patients.

What are the symptoms of lupus?

Symptoms General symptoms. Many of those affected feel sick, tired and exhausted. Joints (arthritis) Joint pain and inflammation of the joints (arthritis) are very common in lupus. Muscles, tendons, bones. Skin. Raynaud’s Syndrome. Heart, circulation and lungs. Blood and lymph. Kidneys.

How does lupus show up?

Systemic lupus erythematosus Those affected often complain of joint and muscle pain. In addition, defects in the mucous membrane can occur in the mouth. In addition, patients suffer from general symptoms such as fever, fatigue, night sweats or weight loss.

Can you detect lupus in the blood?

The diagnosis of SLE should be made by an experienced internal rheumatologist. The most important diagnostic procedures for systemic lupus erythematosus are: anamnesis and physical examination, laboratory tests of blood and urine, X-rays, CT, MRI, EKG, echo and biopsy.

How do you treat lupus?

Cream or ointment: In the case of mild forms of cutaneous lupus erythematosus, the doctor will first try a topical treatment with a cortisone preparation (glucocorticoid) in the form of a cream or ointment for a few weeks.

How dangerous is lupus disease?

Systemic lupus can affect practically all organs. Systemic lupus erythematosus can lead to chronic inflammation of the connective tissue, skin, joints, mucous membranes and blood vessels. Organs and the brain can also be affected. The disease can be correspondingly dangerous.

Can you die of lupus?

If lupus is diagnosed and treated early, patients can have a normal life expectancy. However, there are still patients in whom lupus is fatal. Women with SLE can still get pregnant.

Can lupus attack the brain?

“The diagnosis of“ lupus erythematosus ”is rare, even more rare in children, and extremely rare in children in whom the“ wolf ”- as the translation of“ lupus ”- affects the brain.

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