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For further information, see CMDT Part 20-06: Adult Still Disease
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A systemic form of juvenile chronic arthritis; also occurs in adults
Most adults are in their 20s or 30s; onset after age 60 is rare
High spiking fevers are much more prominent, especially at the outset, than arthritis
The course of adult Still disease can be monophasic, intermittent, or chronic
Macrophage activation syndrome is a life-threatening complication; it can manifest as
Fever
Splenomegaly
Either thrombocytopenia or neutropenia, or both
Hypertriglyceridemia
Hypofibrinogenemia
Marked elevation of serum ferritin
Elevated soluble CD25
Depressed natural killer cell activity
Hemophagocytosis in bone marrow, spleen, and lymph nodes
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Anemia and leukocytosis, with white blood counts sometimes exceeding 40,000/mcL (40 × 109/L)
Serum ferritin levels are often strikingly elevated (> 3000 mg/mL or 6741 pmol/L)
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About half of the patients respond to nonsteroidal anti-inflammatory drugs
Half of patients require prednisone, sometimes in doses > 60 mg/day orally
For patients with refractory disease,