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Adult Onset
Still's Disease
Adult-onset Still's disease is a rare systemic autoinflammatory disease characterized by the classic triad of fevers, joint pain, and a distinctive salmon-colored bumpy rash
Prevalence
Age of Onset
ICD-10
M06.1
Inheritance
Autosomal dominant
Autosomal recessive
Mitochondrial/Multigenic
X-linked dominant
X-linked recessive
5 Facts you should know
FACT
An inflammatory condition that affects multiple organs
FACT
Characterized by the classic triad of fevers, joint pain, and a distinctive salmon-colored bumpy rash
FACT
Other common symptoms include an enlarged spleen and lymph nodes, joint pain, and sore throat
FACT
Levels of the iron-binding protein ferritin are often extremely elevated
FACT
Adult-onset Still's disease is treated with anti-inflammatory medications
Interest over time
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Common signs & symptoms
High fever
Joint pain
Arthritis
Skin rash
Fatigue
Enlarged spleen
Enlarged lymph nodes
High levels of ferritin in the blood
Symptoms may occur continually or over short periods of time. Arthritis can lead to permanent joint damage over time. Some people with AOSD have serious complications that include severe allergic reactions, abnormal blood clotting (disseminated intravascular coagulation), and organ failure.
Current treatments
Treatment for adult-onset Still's disease is focused on managing the symptoms and keeping them from getting worse. Several different types of medications are used including anti-inflammatory medications, steroids, and medications that help control the immune system.[4][5][6]
Specialists that may be involved in the care of someone with adult-onset Still's disease include:
Orthopedist
Rheumatologist
Dermatologist
Canakinumab(Brand name: Ilaris)
Manufactured by Novartis FDA-approved indication: ILARIS is indicated for the treatment of active Still’s disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 years and older. National Library of Medicine Drug Information Portal.
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