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324 Possible Causes for Hepatosplenomegaly, Systemic Juvenile Idiopathic Arthritis

  • Adult-Onset Still Disease

    Other common manifestations of AOSD are lymphadenopathy, hepatosplenomegaly, muscle aches, and pharyngitis.[symptoma.com] The characteristic rash of systemic juvenile idiopathic arthritis is a transient erythematous eruption associated with a quotidian spiking fever.[ncbi.nlm.nih.gov] Adult onset Still's disease (AOSD) is a systemic inflammatory disease characterized by high-fevers, articular involvement, maculopapular rash, hepatosplenomegaly, lymphadenopathy[ncbi.nlm.nih.gov]

  • Juvenile Seronegative Polyarthritis

    Migratory salmon colored light pink rash involving the trunk and/or extremities and hepatosplenomegaly are also frequently observed in patients with systemic onset.[radiopaedia.org] juvenile idiopathic arthritis.[ped-rheum.biomedcentral.com] ., uveitis, rashes, nail changes, lymphadenopathy, hepatosplenomegaly ), laboratory findings, and disease prognosis.[amboss.com]

  • Juvenile-Onset Still Disease

    Appearance of rash, hepatosplenomegaly, serositis and generalized lymphadenopathy.[symptoma.com] Juvenile Idiopathic Arthritis Other forms of Juvenile Idiopathic Arthritis (JIA): The more commonly known forms of Juvenile Idiopathic Arthritis (JIA) are considered to be[autoinflammatory.org] This characteristic diagnostic triad may also be associated with an adenopathy and hepatosplenomegaly.[orpha.net]

  • Cryopyrin-Associated Periodic Syndrome

    Patients may have lymphadenopathy and/or hepatosplenomegaly. The CINCA/NOMID syndrome typically presents shortly after birth.[clevelandclinicmeded.com] In May 2013, it was also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[rarediseases.info.nih.gov] Also approved for the treatment of active Systemic Juvenile Idiopathic Arthritis (SJIA) in patients aged 2 through 16 years.[checkorphan.org]

  • Juvenile Rheumatoid Arthritis

    On admission, he presented with an FUO with hepatosplenomegaly, aseptic meningitis, and pericarditis. An extensive diagnostic workup ruled out lymphoma and leukemia.[ncbi.nlm.nih.gov] 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[periodicfevers.com] Physical and laboratory results showed hepatosplenomegaly, high fever, pancytopenia and impaired liver and renal function tests, elevated triglyceride and serum ferritin levels[ncbi.nlm.nih.gov]

  • Muckle-Wells Syndrome

    She also had hepatosplenomegaly and hyperimmunoglobulinemia, but did not have persistent arthritis, or any neurological or gastrointestinal disorder.[ncbi.nlm.nih.gov] juvenile idiopathic arthritis.[guidetopharmacology.org] Physical exam Remarkable findings include lymphadenopathy and/or hepatosplenomegaly.[symptoma.com]

  • Familial Hemophagocytic Lymphohistiocytosis

    Reported here is the case of a 12-year-old boy, from a poor family, with a 6-year history of visual loss and fever for 5 months, and transient hemiparesis with hepatosplenomegaly[ncbi.nlm.nih.gov] juvenile idiopathic arthritis (sJIA).[ard.bmj.com] Examination revealed fever, lymphadenopathy, and hepatosplenomegaly. Ultrasound examination revealed hepatosplenomegaly and free intra-abdominal fluid.[ncbi.nlm.nih.gov]

  • Polyarticular Juvenile Idiopathic Arthritis

    Migratory salmon colored light pink rash involving the trunk and/or extremities and hepatosplenomegaly are also frequently observed in patients with systemic onset.[radiopaedia.org] Macrophage activation syndrome (MAS) is one of the serious complications associated with rheumatic diseases, especially systemic juvenile idiopathic arthritis (sJIA).[ncbi.nlm.nih.gov] The major difference is the number of joints impacted and the fact that in Systemic Juvenile Idiopathic Arthritis (SJIA), patients experience system wide symptoms, such as[news-medical.net]

  • Multicentric Castleman's Disease

    A 46-year-old man presented with a high-grade fever, multiple lymphadenopathies, hepatosplenomegaly and human immunodeficiency virus (HIV) seropositivity, without severe immunosuppression[ncbi.nlm.nih.gov] She was diagnosed with systemic juvenile idiopathic arthritis (JIA).[ncbi.nlm.nih.gov] Multicentric Castleman's disease (MCD) typically presents with constitutional symptoms, generalized peripheral lymphadenopathy, hepatosplenomegaly, and laboratory markers[ncbi.nlm.nih.gov]

  • Mevalonate Kinase Deficiency

    Patient N.M. manifested minor anomalies, hepatosplenomegaly, anemia, thrombocytopenia, recurrent febrile crises, and facial rashes.[ncbi.nlm.nih.gov] A wide variety of diseases had been suspected: systemic juvenile idiopathic arthritis, periodic fever aphtous stomatitis pharyngitis adenitis syndrome, other hereditary recurrent[ncbi.nlm.nih.gov] The extra-articular symptoms started at 3 months (1974) with flares occurring at irregular intervals; atypical systemic juvenile idiopathic arthritis (aSJIA) was diagnosed[academic.oup.com]

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