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Sarcoidosis
Sarcoidosis

... Clinical Manifestations • 50% patients are asymptomatic • Abnormal "routine" chest radiograph • Symptomatic patients, with wide variety of symptoms • Onset is usually insidious but can be acute ...
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No Slide Title

... • Interstitial lung disease does not explain pulm htn • Diffusing capacity does not correlate with pulm htn • DLCO decreased in pulm htn secondary to fibrocystic pulm sarcoidosis ...
SARCOIDOSIS SARCOIDOSIS GLOSSARY OF TERMS ACE
SARCOIDOSIS SARCOIDOSIS GLOSSARY OF TERMS ACE

... reaction  occurs  against  the  body’s  own  cells  or  tissues,  it  is  called  an  autoimmune  reaction.   Immune  system  —  A  complex  system  of  molecules  and  blood  cells  that  protect  the  body  from   germs,  such  as ...
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Sarcoidosis



Sarcoidosis, also called sarcoid, is a disease involving abnormal collections of inflammatory cells (granulomas) that can form as nodules in multiple organs. The granulomas are most often located in the lungs or its associated lymph nodes, but any organ can be affected. Sarcoidosis seems to be caused by an immune reaction to an infection or some other trigger (called an antigen) that continues even after the initial infection or other antigen is cleared from the body. In most cases it clears up by itself without any medical intervention, but some cases go on to affect the person long-term or become life-threatening and require medical intervention, most often with medications. 1 alpha, 25(OH)2 Vitamin D3 is the main cause for high blood calcium in sarcoidosis and is overproduced by sarcoid granulomata. Gamma-interferon produced by activated lymphocytes and macrophages plays a major role in the synthesis of 1 alpha, 25(OH)2 Vitamin D3.Treatment is usually designed to help relieve the symptoms and thus does not directly alter the course of the disease. This treatment usually consists of anti-inflammatory drugs like ibuprofen or aspirin. In cases where the condition develops to the point that it has a progressive and/or life-threatening course, the treatment is most often steroid treatment with prednisone or prednisolone. Alternatively, drugs that are most commonly used to treat cancer and suppress the immune system, such as methotrexate, azathioprine and leflunomide, may be used. The average mortality rate is less than 5% in untreated cases.In the United States it most commonly affects people of Northern European (especially Scandinavian or Icelandic) or African/African American ancestry between the ages of 20 and 29, although any race or age group can be affected. Japan has a lower rate of sarcoidosis than the United States, although in these people the disease is usually more aggressive in its course with the heart often affected. Japanese individuals also have a different peak age for sarcoidosis, 25–40 years of age. It occurs about twice as often in women, where it usually takes a more aggressive course. In developing countries, it often goes misdiagnosed as tuberculosis (TB) as its symptoms often resemble those of TB.Sarcoidosis was first described in 1877 by an English doctor named Dr. Jonathan Hutchinson as a skin disease causing red, raised lesions on the arms, face, and hands.
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