Overview

Sarcoidosis is a disease characterized by the growth of tiny collections of inflammatory cells (granulomas) in any part of your body — most commonly the lungs and lymph nodes. But it can also affect the eyes, skin, heart and other organs.

The cause of sarcoidosis is unknown, but experts think it results from the body's immune system responding to an unknown substance. Some research suggests that infectious agents, chemicals, dust and a potential abnormal reaction to the body's own proteins (self-proteins) could be responsible for the formation of granulomas in people who are genetically predisposed.

There is no cure for sarcoidosis, but most people do very well with no treatment or only modest treatment. In some cases, sarcoidosis goes away on its own. However, sarcoidosis may last for years and may cause organ damage.

Symptoms

Signs and symptoms of sarcoidosis vary depending on which organs are affected. Sarcoidosis sometimes develops gradually and produces symptoms that last for years. Other times, symptoms appear suddenly and then disappear just as quickly. Many people with sarcoidosis have no symptoms, so the disease may be discovered only when a chest X-ray is done for another reason.

General symptoms

Sarcoidosis can begin with these signs and symptoms:

  • Fatigue
  • Swollen lymph nodes
  • Weight loss
  • Pain and swelling in joints, such as the ankles

Lung symptoms

Sarcoidosis most often affects the lungs and may cause lung problems, such as:

  • Persistent dry cough
  • Shortness of breath
  • Wheezing
  • Chest pain

Skin symptoms

Sarcoidosis may cause skin problems, which may include:

  • A rash of red or reddish-purple bumps, usually located on the shins or ankles, which may be warm and tender to the touch
  • Disfiguring sores (lesions) on the nose, cheeks and ears
  • Areas of skin that are darker or lighter in color
  • Growths under the skin (nodules), particularly around scars or tattoos

Eye symptoms

Sarcoidosis can affect the eyes without causing any symptoms, so it's important to have your eyes checked regularly. When eye signs and symptoms do occur, they may include:

  • Blurred vision
  • Eye pain
  • Burning, itching or dry eyes
  • Severe redness
  • Sensitivity to light

Heart symptoms

Signs and symptoms related to cardiac sarcoidosis may include:

  • Chest pain
  • Shortness of breath (dyspnea)
  • Fainting (syncope)
  • Fatigue
  • Irregular heartbeats (arrhythmias)
  • Rapid or fluttering heart beat (palpitations)
  • Swelling caused by excess fluid (edema)

Sarcoidosis can also affect calcium metabolism, the nervous system, the liver and spleen, muscles, bones and joints, the kidneys, lymph nodes, or any other organ.

When to see a doctor

See your doctor if you have signs and symptoms of sarcoidosis.

"My experience at Mayo has helped me be here for my grandkids."

— Jim, patient, sarcoidosis

Jim, patient: We were given two beautiful grandkids there shortly after retirement. They are two special little girls and that really makes life nice. I never had a symptom until that first day of the actual heart attack. I was 100 percent blocked.

Diana, spouse: They put 2 or 3 stents in — the doctors would — and then within months, Jim would have the same kind of symptoms again.

Jim: I was in the hospital again and this time, it was open-heart surgery.

Diana: Oh, my gosh, when he opened Jim up, he said I've seen something today that I've never seen on anybody.

Jim: It was discovered at that time that I had sarcoidosis.

Diana: You're going to have to go to the Mayo Clinic.

Leslie Cooper, M.D., Mayo Clinic Cardiology: He had rapid re-narrowing to the arteries to his heart after they had placed stents. In his case, they were related to an autoimmune disease, sarcoidosis.

Diana: The treatment, the doctors, the teamwork was unbelievable.

Leslie Cooper, M.D.: We took an established drug in another area and applied it for the first time in cardiac sarcoidosis.

Diana: It was experimental, but it put that sarcoid into remission and that gave Jim his life back. It turned out to be a really good risk.

Jim: I didn't realize that the Mayo Clinic was so accessible. When I go there I have no doubt that I'm going to meet competent people in their work and their field. That, I think, gives you the confidence to trust that you are going to be okay. My experience at Mayo I think has helped me be here for my grandkids. I'm just so thankful to be here.

From Mayo Clinic to your inbox

Sign up for free and stay up to date on research advancements, health tips, current health topics, and expertise on managing health. Click here for an email preview.

To provide you with the most relevant and helpful information, and understand which information is beneficial, we may combine your email and website usage information with other information we have about you. If you are a Mayo Clinic patient, this could include protected health information. If we combine this information with your protected health information, we will treat all of that information as protected health information and will only use or disclose that information as set forth in our notice of privacy practices. You may opt-out of email communications at any time by clicking on the unsubscribe link in the e-mail.

Causes

Doctors don't know the exact cause of sarcoidosis. Some people appear to have a genetic predisposition to develop the disease, which may be triggered by bacteria, viruses, dust or chemicals.

This triggers an overreaction of your immune system, and immune cells begin to collect in a pattern of inflammation called granulomas. As granulomas build up in an organ, the function of that organ can be affected.

Risk factors

While anyone can develop sarcoidosis, factors that may increase your risk include:

  • Age and sex. Sarcoidosis can occur at any age, but often occurs between the ages of 20 and 60 years. Women are slightly more likely to develop the disease.
  • Race. People of African descent and those of Northern European descent have a higher incidence of sarcoidosis. African-Americans are more likely to have involvement of other organs along with the lungs.
  • Family history. If someone in your family has had sarcoidosis, you're more likely to develop the disease.

Complications

Sometimes sarcoidosis causes long-term problems.

  • Lungs. Untreated pulmonary sarcoidosis can lead to permanent scarring in your lungs (pulmonary fibrosis), making it difficult to breathe and sometimes causing pulmonary hypertension.
  • Eyes. Inflammation can affect almost any part of your eye and may cause damage to the retina, which can eventually cause blindness. Rarely, sarcoidosis also can cause cataracts and glaucoma.
  • Kidneys. Sarcoidosis can affect how your body handles calcium, which can lead to kidney stones and reduce kidney function. Rarely, this can lead to kidney failure.
  • Heart. Cardiac sarcoidosis results in granulomas in your heart that can disrupt heart rhythm, blood flow and normal heart function. In rare instances, this may lead to death.
  • Nervous system. A small number of people with sarcoidosis develop problems related to the central nervous system when granulomas form in the brain and spinal cord. Inflammation in the facial nerves, for example, can cause facial paralysis.

Jan. 30, 2019
  1. Sarcoidosis. National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov/health-topics/sarcoidosis. Accessed Nov. 16, 2018.
  2. AskMayoExpert. Sarcoidosis. Rochester, Minn.: Mayo Foundation for Medical Education and Research; 2018.
  3. Sarcoidosis. Merck Manual Professional Version. https://www.merckmanuals.com/professional/pulmonary-disorders/sarcoidosis/sarcoidosis. Accessed Nov. 16, 2018.
  4. Raevis JJ, et al. Ocular involvement in sarcoidosis. Journal of Rheumatology. 2018;45:580.
  5. Froehlich W, et al. Cardiac sarcoidosis. Circulation. 2015;132:e137.
  6. AskMayoExpert. Cardiac sarcoidosis. Rochester, Minn.: Mayo Foundation for Medical Education and Research; 2018.
  7. Ferri FF. Sarcoidosis. In: Ferri's Clinical Advisor 2019. Philadelphia, Pa.: Elsevier; 2019. https://www.clinicalkey.com. Accessed Nov. 16, 2018.
  8. Goldman L, et al., eds. Sarcoidosis. In: Goldman-Cecil Medicine. 25th ed. Philadelphia, Pa.: Saunders Elsevier; 2016. https://www.clinicalkey.com. Accessed Nov. 16, 2018.
  9. Carmona EM, et al. Pulmonary sarcoidosis: Diagnosis and treatment. Mayo Clinic Proceedings. 2016;91:946.
  10. Strookappe B, et al. Physical activity and training in sarcoidosis: Review and experience-based recommendations. Expert Review of Respiratory Medicine. 2016;10:1057.
  11. Yatsynovich Y, et al. Cardiac sarcoidosis: A review of contemporary challenges in diagnosis and treatment. American Journal of the Medical Sciences. 2018;355:113.
  12. Noe MH, et al. Cutaneous sarcoidosis. Current Opinion in Pulmonary Medicine. 2017;23:482.
  13. Ramachandraiah V, et al. Pulmonary sarcoidosis: An update. Postgraduate Medicine. 2017;129:149.
  14. Arkema EV, et al. Epidemiology of sarcoidosis: Current findings and future directions. Therapeutic Advances in Chronic Disease. 2018;9:227.
  15. Bargagli E, et al. Sarcoidosis: A review for the internist. Internal and Emergency Medicine. 2018;13:325.
  16. Atkins C, et al. Managing fatigue in sarcoidosis ― A systematic review of the evidence. Chronic Respiratory Disease. 2017;14:161.
  17. FSR's self-care guide. Foundation for Sarcoidosis Research. https://www.stopsarcoidosis.org/good-self-care/self-care-guide/#. Accessed Nov. 28, 2018.
  18. Utz JP (expert opinion). Mayo Clinic, Rochester, Minn. Dec. 12, 2018.
  19. Moua T (expert opinion). Mayo Clinic, Rochester, Minn. Dec. 12, 2018.
  20. Carmona Porquera EM (expert opinion). Mayo Clinic, Rochester, Minn. Dec. 19, 2018.

Related

Associated Procedures

Products & Services