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Adult-onset Still's disease is a rare disease of inflammation. It often causes a fever every day, joint pain and a pink rash that comes and goes.

Adult-onset Still’s disease (AOSD) is a rare disease that causes inflammation, or swelling, in the body. It usually causes three main signs:
The name comes from Still’s disease in children. Doctors call that systemic juvenile idiopathic arthritis. When the same pattern starts after age 16, it is called adult-onset Still’s disease.
The innate immune system is the body’s first line of defense. In AOSD, it works too hard. It sends out large amounts of signals that cause inflammation. That inflammation causes the fever, rash and joint pain. It can also affect organs such as the liver, spleen, lymph nodes, the lining of the heart and the lungs.
AOSD is different for each person. Some people have one bout that calms down. Some have flares with quiet times in between. Some have joint disease that lasts a long time.
AOSD is rare. It most often starts in young adults, between about 15 and 35 years old. But it can start later in life. Both women and men get it. No one knows the cause. Researchers think genes may play a part. Triggers, such as infections, may also play a part.
No single test can show AOSD. A rheumatologist looks at the pattern of your symptoms. They also rule out infections, cancers and other rheumatic diseases that can look the same. Tests often include:
Treatment aims to calm the inflammation and ease your symptoms. It also protects your joints and organs. Your rheumatologist chooses medicines based on how active the disease is. They may use:
Regular checkups and blood tests help your care team see how well treatment works. They change it over time as needed.
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