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357 Possible Causes for Eruptions, Systemic Juvenile Idiopathic Arthritis

  • Adult-Onset Still Disease

    Therefore, biopsy of atypical eruptions in AOSD patients is recommended because it is likely that the highly distinctive histopathologic features will allow these eruptions[] The characteristic rash of systemic juvenile idiopathic arthritis is a transient erythematous eruption associated with a quotidian spiking fever.[] ISSN 1546-0096 Abstract Background: Adult-onset Still’s disease (AOSD), a rare autoinflammatory disorder, resembles systemic juvenile idiopathic arthritis (SJIA).[]

  • Juvenile-Onset Still Disease

    In the remaining cases, the arthritis persists, with or without fever and cutaneous eruption.[] Juvenile Idiopathic Arthritis Other forms of Juvenile Idiopathic Arthritis (JIA): The more commonly known forms of Juvenile Idiopathic Arthritis (JIA) are considered to be[] Other, less frequently observed lesions include urticaria and urticaria-like eruptions, generalized or widespread non-pruritic persistent erythema, vesiculopustular eruptions[]

  • Cryopyrin-Associated Periodic Syndrome

    Fever, limb pain, conjunctivitis, and elevation of acute phase reactants are usually associated with skin eruption.[] 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.[]

  • Muckle-Wells Syndrome

    Muckle-Wells syndrome is characterized by a recurrent urticarial eruption that is associated with episodic fever, myalgia, arthralgia, malaise, progressive sensorineural hearing[] juvenile idiopathic arthritis.[] Three main features of the disease are: (i) urticarial eruptions; (ii) progressive perceptive deafness; and (iii) amyloid nephropathy.[]

  • Multicentric Castleman's Disease

    A 65-year-old man was admitted with relapsing and remitting fever, scattered skin eruptions and hepatosplenomegaly following combination antiretroviral therapy for his HIV[] She was diagnosed with systemic juvenile idiopathic arthritis (JIA).[] […] or thrombocytosis, hypoalbuminemia, renal dysfunction or proteinuria, polyclonal hypergammaglobulinemia, constitutional symptoms, hepatosplenomegaly, effusions or edema, eruptive[]

  • CINCA Syndrome

    The syndrome is characterized by a generalized, wandering palpable rash eruption of neonatal onset, chronic arthropathy characterized by abnormal proliferation of cartilage[] juvenile idiopathic arthritis (SJIA) are rare systemic disorders of auto-inflammatory nature.[] Three main manifestations of CINCA syndrome are cutaneous signs, including maculopapular urticarial eruptions, commonly observed in the infantile period, joint involvement[]

  • Schnitzler Syndrome

    Systemic steroids may be somewhat effective at controlling the cutaneous eruption, but usually at doses that can cause significant, long-term adverse effects.[] Cryopyrin associated periodic syndrome, CAPS), systemic Juvenile Idiopathic Arthritis and gout.[] TCZ treatment has proved to be very effective, well-tolerated and safe in other acquired autoinflammatory disorders, systemic juvenile idiopathic arthritis (sJIA) and adult-onset[]

  • Herpes Zoster

    Acute inciting events for this eruption are not always known, but can include illness, stress, and mechanical injury.[] In children, pars planitis should be differentiated from chronic anterior uveitis which may be idiopathic or associated with juvenile idiopathic arthritis (JIA).[] We report a case of mycosis fungoides proved by biopsy and immunohistochemistry that developed in a 55-year-old man at the site of previous herpes zoster eruption.[]

  • Juvenile Temporal Arteritis

    Three years later, a new eruption, again asymptomatic, appeared in the posterior region of the patient's right ear. Subsequently, she was referred to our department.[] The intravenous formulation is approved for the treatment of moderate to severely active rheumatoid arthritis, systemic juvenile idiopathic arthritis, and polyarticular juvenile[] There were no systemic symptoms other than eruptions. Inflammatory indicators, including CRP, were not elevated.[]

  • Juvenile Rheumatoid Arthritis

    Symptoms of early onset sarcoidosis characterized by skin eruptions, arthritis, and uveitis mimic those of systemic type juvenile rheumatoid arthritis (JRA).[] S: Systemic Whole body is affected J: Juvenile Begins in childhood I: Idiopathic Cause is unknown A: Arthritis Joint inflammation SJIA (systemic juvenile idiopathic arthritis[] Mean ( SD) age of attainment of different stages of genitalia development as well as for eruption of hair was ascertained amongst boys who entered puberty using conventional[]

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