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Sarcoidosis

Sarcoid, stage I - chest X-ray
Sarcoid, stage I - chest X-ray
Sarcoid, stage II - chest X-ray
Sarcoid, stage II - chest X-ray
Sarcoid, stage IV - chest X-ray
Sarcoid, stage IV - chest X-ray
Sarcoid - close-up of the skin lesions
Sarcoid - close-up of the skin lesions
Erythema nodosum associated with sarcoidosis
Erythema nodosum associated with sarcoidosis
Sarcoidosis - close-up
Sarcoidosis - close-up
Sarcoidosis on the elbow
Sarcoidosis on the elbow
Sarcoidosis on the nose and forehead
Sarcoidosis on the nose and forehead
Respiratory system
Respiratory system

Definition

  

Sarcoidosis is a disease of unknown cause in which inflammation occurs in the lymph nodes, lungs, liver, eyes, skin, or other tissues.


Causes, incidence, and risk factors

  

The cause of the disease is unknown. Sarcoidosis is marked by abnormal inflammatory masses (granulomas) in certain organs of the body. Granulomas are clusters of immune cells (macrophages, lymphocytes, and multinucleated giant cells). The disease can affect almost any organ of the body, although it most commonly affects the lungs. Sarcoidosis can be acute, subacute, or chronic.

Possible causes of sarcoidosis include:

  • Hypersensitivity to environmental factors
  • Genetics
  • Extreme immune response to infection

The incidence varies widely according to race and sex.

It is more common in African Americans than Caucasians. Females are usually affected more frequently than males. Onset of the disease typically occurs between the ages of 20 and 40. Sarcoidosis is very rare in young children.


Symptoms

  

Additional symptoms of this disease:

Note: There may be no symptoms. Most of the time, the disease is found in patients with no symptoms who have an abnormal chest x-ray.


Signs and tests

  

This disease may also alter the results of the following tests:


Treatment

  

Sarcoidosis symptoms often resolve on their own gradually without treatment.

Severely affected patients may need treatment with corticosteroids. Therapy may continue for one or two years. Some of the most severely affected patients may require life-long therapy.

Immunosuppressive agents, such as methotrexate, azathioprine, and cyclophosphamide, are sometimes used in addition to corticosteroids. Rarely, some individuals with irreversible organ failure require an organ transplant.


Support Groups

  


Expectations (prognosis)

  

Many people are not seriously ill, and the disease may resolve without treatment. About 30 - 50% of cases resolve without treatment in 3 years. About 20% of those with lung involvement will develop lung damage. Death from sarcoidosis is rare.


Complications

  

Calling your health care provider

  

Call your health care provider if you have difficulty breathing, vision changes, palpitations, or other symptoms of this disorder.


Prevention

  


References

  

Goldman L, Ausiello D. Cecil Textbook of Medicine. 22nd ed. Philadelphia, Pa:Saunders; 2003.

Cox CE, Donohue JF, Brown CD, Kataria YP, Judson MA. Health-related quality of life of persons with sarcoidosis. Chest. March 2004;125:997-1004.

Cox CE, Davis-Allen A, Judson MA. Sarcoidosis. Med Clin North Am. July 2005;89:817-828.


 
Review Date: 3/1/2007
Reviewd By: David A. Kaufman, M.D., Assistant Professor, Division of Pulmonary Medicine, Mount Sinai School of Medicine, New York, NY. Review provided by VeriMed Healthcare Network.
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