- Chest pain (most often behind the breast bone)
- Dry cough
- Shortness of breath
- Coughing up blood (rare, but serious)
- Joint ache or pain (arthralgia)
- Raised, red, firm skin sores (erythema nodosum), almost always on the front part of the lower legs
- Scars that become raised or inflamed
- Weakness on one side of the face
- Discharge from the eye
- Dry eyes
- Vision loss
- Dry mouth
- Fainting spells, if the heart is involved
- Swelling in the upper part of the abdomen
- Liver disease
- Abnormal breath sounds (such as rales)
- Enlarged liver
- Enlarged lymph glands
- Enlarged spleen
- Eye inflammation (specialized eye exam is needed)
- Chest x-ray to see if the lungs are involved or lymph nodes are enlarged
- CT scan of the chest
- Lung gallium scan
- Imaging tests of the brain and liver
- Echocardiogram of the heart
- Bleeding from the lung tissue
- Heart damage, leading to heart failure and abnormal heart rhythms
- Lung scarring (pulmonary fibrosis)
- Vision changes
- Other symptoms of this disorder
Sarcoidosis is a disease in which inflammation occurs in the lymph nodes, lungs, liver, eyes, skin, or other tissues.
The exact cause of sarcoidosis is unknown. What is known is that when a person has the disease, tiny clumps of abnormal tissue (granulomas) form in certain organs of the body. Granulomas are clusters of immune cells.
The disease can affect almost any organ. It most commonly affects the lungs.
Doctors think that having certain genes makes it more likely for a person to develop sarcoidosis. Things that may trigger the disease include infections with bacteria or viruses. Contact with dust or chemicals may also be triggers.
The disease is more common in African Americans and Caucasians of Scandinavian heritage. More women than men have the disease.
The disease often begins between ages 20 and 40. Sarcoidosis is rare in young children.
A person with a close blood relative who has sarcoidosis is nearly five times as likely to develop the condition.
There may be no symptoms. When symptoms do occur, they can involve almost any body part or organ system.
Almost all people affected by sarcoidosis have lung or chest symptoms:
Symptoms of general discomfort:
Nervous system symptoms may include:
Eye symptoms include:
Other symptoms of this disease:
Exams and Tests
A physical exam may show the following:
The disease is often found in people without visible physical signs who have an abnormal chest x-ray.
Different imaging tests may help diagnose sarcoidosis:
To diagnose this condition, a biopsy is needed. Biopsy of the lung using bronchoscopy is usually done. Biopsies of other body tissues may also be done.
The following lab tests may be done:
Sarcoidosis symptoms will often get better without treatment.
If the eyes, heart, nervous system, or lungs are affected, corticosteroid medicine is usually prescribed. This medicine may need to be taken for 1 to 2 years.
Medicines that suppress the immune system (immunosuppressive medicines) are sometimes also needed.
In rare cases, people with very severe heart or lung damage (end-stage disease) may need an organ transplant.
Many people with sarcoidosis are not seriously ill, and they get better without treatment. Up to half of all people with the disease get better in 3 years without treatment. People whose lungs are affected may develop lung damage.
Overall death rate from sarcoidosis is less than 5%. Causes of death include:
When to Contact a Medical Professional
Call your health care provider promptly if you have:
Judson MA, Morgenthau AS, Baughman RP. Sarcoidosis. In: Broaddus VC, Mason RJ, Ernst JD, et al, eds. Murray and Nadel's Textbook of Respiratory Medicine. 6th ed. Philadelphia, PA: Elsevier Saunders; 2016:chap 66.
Valeyre D, Prasse A, Nunes H, Uzunhan Y, Brillet PY, Müller-Quernheim J. Sarcoidosis. Lancet. 2014; 383(9923):1155-1167. PMID: 24090799 www.ncbi.nlm.nih.gov/pubmed/24090799.
- Review date:
- December 07, 2016
- Reviewed by:
- Denis Hadjiliadis, MD, MHS, Associate Professor of Medicine, Pulmonary, Allergy, and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA. Also reviewed by David Zieve, MD, MHA, Isla Ogilvie, PhD, and the A.D.A.M. Editorial team.
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