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207 Possible Causes for Leukocytes Increased, Systemic Juvenile Idiopathic Arthritis

  • 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[] . - Increased number of white cells (leukocytes, especially neutrophils) and a minor criteria: - A sore throat that can be severe, constant, and burning - Lymphadenopathy[] Systemic-onset juvenile idiopathic arthritis Specialty Pediatrics/rheumatology Systemic-onset juvenile idiopathic arthritis (also known as systemic juvenile idiopathic arthritis[]

  • Septic Arthritis

    This infection is endemic in some parts of the world (North USA and central Europe) and most common cause of chronic arthritis (more common than Juvenile Idiopathic Arthritis[] […] likelihood of septic arthritis (LR 7.7 positive; LR 0.42 negative) At least 90% leukocytes (LR 3.4 positive; LR 0.34 negative) Low WBC count common in immunosuppressed patients[] Gallium and indium scans also show increased isotope uptake in areas of concentrated polymorphonuclear leukocytes, macrophages, and malignant tumors.[]

  • Adult-Onset Still Disease

    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).[] Comparison of long term evolution of adult onset and juvenile onset Still’s disease, both followed up for more than 10 years. Ann Rheum Dis. 1990;49:283–5.[]

  • 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[]

  • Kawasaki Disease

    juvenile idiopathic arthritis.[] ) (37.7 sec), elevated level of GGT (2.04 ukat/l) and increased titters of specific IgM antibodies for Adenovirus and Epstein Barr virus.[] […] and connective tissue ( M, 710-739 ) Arthropathies Arthritis ( Septic arthritis, Reactive arthritis, Rheumatoid arthritis, Psoriatic arthritis, Felty's syndrome, Juvenile[]

  • Enthesitis-Related Arthritis

    juvenile idiopathic arthritis (JIA) rash.[] Risk Factors Genetics Rare in siblings, but many studies have demonstrated increased frequencies of various human leukocyte antigen markers in JIA.[] Using the International League of Associations for Rheumatology (ILAR) system for juvenile idiopathic arthritis, most childhood SpA is classified as enthesitis-related arthritis[]

  • CINCA Syndrome

    juvenile idiopathic arthritis (SJIA) are rare systemic disorders of auto-inflammatory nature.[] However, there is an increased occurrence of Non-Hodgkin's lymphoma (risk factors are persistently low lymphocytes (one type of leukocyte) in blood and low complement factors[] Cerebral spinal fluid (CSF) examination demonstrates variable hypercellularity with increased polymorphonuclear leukocytes, elevated protein levels, and an increased opening[]

  • Temporal Arteritis

    Intravenous Actemra was also previously approved for the treatment of moderate to severely active rheumatoid arthritis, systemic juvenile idiopathic arthritis and polyarticular[] Using immunochemical staining, Cid et al demonstrated that different adhesion molecules might regulate how leukocytes and endothelial cells interact in different temporal[] Subcutaneous Actemra was previously approved for the treatment of moderate to severely active rheumatoid arthritis.[]

  • Juvenile Rheumatoid Arthritis

    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[] Several genetic risk loci have been identified conferring increased susceptibility to JIA, many within the human leukocyte antigen region.[] BM was hypercellular with increased numbers of myeloid precursors and megakaryocytes.[]

  • Familial Cold Autoinflammatory Syndrome Type 1

    In May 2013, it was also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[] Lesional biopsy demonstrated polymorphonuclear infiltration with increased eosinophils.[] Other autoinflammatory diseases that do not have clear genetic causes include adult-onset Still's disease, systemic-onset juvenile idiopathic arthritis, Schnitzler syndrome[]

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