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86 Possible Causes for Exanthema, Systemic Juvenile Idiopathic Arthritis

  • Adult-Onset Still Disease

    The characteristic rash of systemic juvenile idiopathic arthritis is a transient erythematous eruption associated with a quotidian spiking fever.[] Definition / general Rare systemic inflammatory disease accompanied by a triad of spiking fever, maculopapular exanthema and arthralgia, accompanied frequently by lymphadenopathy[] ISSN 1546-0096 Abstract Background: Adult-onset Still’s disease (AOSD), a rare autoinflammatory disorder, resembles systemic juvenile idiopathic arthritis (SJIA).[]

  • Juvenile Seronegative Polyarthritis

    juvenile idiopathic arthritis.[] […] described seven types of juvenile idiopathic arthritis.[] Disease, Juvenile Onset Stills Disease, Juvenile-Onset Still's Disease, Juvenile-Onset Stills Disease, Still Disease, Juvenile Onset, Still Disease, Juvenile-Onset, Still's[]

  • Juvenile-Onset Still Disease

    Juvenile Idiopathic Arthritis Other forms of Juvenile Idiopathic Arthritis (JIA): The more commonly known forms of Juvenile Idiopathic Arthritis (JIA) are considered to be[] Systemic-onset juvenile idiopathic arthritis Specialty Pediatrics/rheumatology Systemic-onset juvenile idiopathic arthritis (also known as systemic juvenile idiopathic arthritis[] onset Still's disease, both followed up for more than 10 years.[]

  • Cryopyrin-Associated Periodic Syndrome

    In May 2013, it was also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[] Also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[] Canakinumab is also used to treat active systemic juvenile idiopathic arthritis (SJIA) in children 2 years of age and older.[]

  • Kawasaki Disease

    juvenile idiopathic arthritis.[] […] of these 25 (68%) lacked two of the six principal symptoms of Kawasaki disease, with the most frequently missing symptoms being cervical lymphadenopathy and polymorphous exanthema[] […] bilateral non-exudative conjunctivitis, redness and swelling of the tongue, lips and oral mucosa, abnormalities in the extremities, cervical lymph node, and polymorphic exanthema[]

  • CINCA Syndrome

    juvenile idiopathic arthritis (SJIA) are rare systemic disorders of auto-inflammatory nature.[] […] onset juvenile idiopathic arthritis which shares many aspects with CINCA but it is rare in the first 6 months of life.[] […] onset juvenile idiopathic arthritis, hyper-immunoglobulinemia D syndrome, sweet syndrome, mastocytosis and Langerhan's cell histiocytosis.[]

  • Herpes Zoster

    In children, pars planitis should be differentiated from chronic anterior uveitis which may be idiopathic or associated with juvenile idiopathic arthritis (JIA).[] The exanthema crusts over within 7-10 days, mostly healing completely, in severe blistering, however, scars and skin discoloring might remain. 5 Diagnosis visual examination[] ., which is often subsequently clearer, once neuritis and vesicular exanthema –common HZ symptoms– develop.[]

  • Rheumatoid Arthritis

    JIA 2016 EULAR/ACR/PRINTO Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis Complete Article Myositis Classification[] De Benedetti F et al (2001) Effect of IL-6 on IGF binding protein-3: a study in IL-6 transgenic mice and in patients with systemic juvenile idiopathic arthritis.[] Classification Henoch-Schoenlein Purpura Classification Hypersensitivity Vasculitis Classification JRA Definition of Improvement Macrophage Activation Syndrome Classification - Systemic[]

  • Henoch-Schönlein Purpura

    This case, along with prior reports of dilated coronaries in systemic juvenile idiopathic arthritis (SJIA), highlights the importance of considering other sources of systemic[] She had pruritic maculopapular exanthema on her legs.[] Fliegner, 17-jähriger Mann mit akuten Bauchschmerzen, Hämatochezie und Exanthem 17 year old patient with acute abdominal pain, hematochezia and exanthema, Der Internist, 10.1007[]

  • Acrodynia

    juvenile idiopathic arthritis or polyarteritis nodosa), or acrodynia (for example, a mercury hypersensitivity reaction).[] […] adenovirus, measles, Rocky Mountain spotted fever, or leptospirosis), drug reaction (for example, to antibiotics, anticonvulsants, or antifungals), autoimmune disease (such as systemic[]

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