Abstract
Adult-onset Still’s disease is an uncommon autoimmune
inflammatory disease, most often seen in young adults.
it presents as a combination of systemic manifestations typically
including spiking fevers, short-lived rashes, and joint symptoms
ranging from arthralgia to aggressive arthritis.
no specifc diagnostic test is available; the clinical diagnosis is
based on pattern recognition and exclusion.
the disease remits in a third of patients, whereas a debilitating
disease course is mainly seen in those with root joint involvement.
modern treatment options include monoclonal antibodies that
inhibit cytokine effects; however, there is a striking lack of clinical
trials.
inflammatory disease, most often seen in young adults.
it presents as a combination of systemic manifestations typically
including spiking fevers, short-lived rashes, and joint symptoms
ranging from arthralgia to aggressive arthritis.
no specifc diagnostic test is available; the clinical diagnosis is
based on pattern recognition and exclusion.
the disease remits in a third of patients, whereas a debilitating
disease course is mainly seen in those with root joint involvement.
modern treatment options include monoclonal antibodies that
inhibit cytokine effects; however, there is a striking lack of clinical
trials.
Original language | English |
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Title of host publication | Rheumatology |
Editors | Marc Hochberg, Alan Silman, Joseph Smolen |
Place of Publication | Philadelphia |
Publisher | Elsevier - Mosby |
Chapter | 84 |
Number of pages | 10 |
Edition | 5th |
ISBN (Print) | 9780323065511 |
Publication status | Published - 29 Oct 2011 |