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19 Possible Causes for Eosinophils Increased, Hemochromatosis, Hypocomplementemia

  • Systemic Lupus Erythematosus

    PATIENT CONCERNS: In rare cases, pleural eosinophilia is associated with connective tissue disease.[] She also had concomitant massive hematuria and proteinuria, fever, multiple positive autoimmune antibodies, hypocomplementemia, abnormal lumbar puncture findings and evidence[] Laboratory findings on admission revealed proteinuria, microscopic hematuria, anemia, leukopenia, hypoalbuminemia, hypocomplementemia, and slightly elevated levels of serum[]

  • Sjogren's Syndrome

    Blood tests may reveal elevated erythrocyte sedimentation rate and transaminase levels, anemia, leukopenia, eosinophilia, hypergammaglobulinemia, presence of antinuclear antibodies[] Leukocytoclastic cutaneous vasculitis, hypocomplementemia, and HCV infection are associated with the presence of cryoglobulins in the sera of patients with primary SS.[] […] lacrimal gland deficiencies that may impair aqueous production include the following: Lacrimal gland infiltration Sarcoidosis Lymphoma AIDS Graft vs host disease Amyloidosis Hemochromatosis[]

  • Complement Deficiency Syndrome

    Workup often shows hypocomplementemia ( C3/C4), renal failure, eosinophilia and eosinophiluria.[] BLD04 is a completely new gene set for the diagnosis of Hemochromatosis . BLD05 is also a new gene set for VB12-dependent megaloblastic anemia .[] Syndrome Hyper IgE Syndrome (HIES) is a rare primary immunodeficiency disease characterized by eczema, recurrent staphylococcal skin abscesses, recurrent lung infections, eosinophilia[]

  • Rheumatoid Arthritis

    Abstract Biologics used in the treatment of rheumatoid arthritis (RA) rarely cause eosinophilia.[] Hypocomplementemia in rheumatoid arthritis. Am J Med 1973 ; 54 : 461 –72. Geirsson A , Sturfelt G, Truedsson L.[] Hemochromatosis may cause hand joint arthritis.[]

  • Carcinomatous Polyarthritis

    […] be paraneoplastic Tender migrating edema Keys - NO Raynauds, follows exercise, nl nailfold capillaries Peau d'orange skin in prox forearms, upper legs Labs - peripheral eosinophilia[] SLE may manifest with hypocomplementemia, lymphopenia, and thrombocytopenia; a low haptoglobin with elevated LDH in this disease may suggest immune mediated hemolysis.[] ’s disease Fungal arthritis Gaucher’s disease Giant cell arteritis Gonococcal arthritis Goodpasture’s syndrome Gout Granulomatous arteritis Haemochromatosis Hemarthrosis Hemochromatosis[]

  • Systemic Disease

    The patient presented with hypertension, a raised serum creatinine, proteinuria, elevated serum IgG4, and eosinophilia.[] Although the patient had hypocomplementemia and was positive for antinuclear antibodies, he was negative for antibodies against Sm, SS-A, SS-B and RNP, and his anti-DNA antibody[] Koilonychia, or “spoon-shaped” nails, may stimulate a work-up for hemochromatosis or anemia.[]

  • Immune Complex Disease

    Release of mediators leads to increased vascular permeability, edema, smooth muscle contraction, platelet aggregation.[] 19 F with fever, raised inflammatory markers and hypocomplementemia- Differential diagnosis here are- 1. Immune complex disease- SLE or glomerulonephritis 2.[] From a clinical standpoint, these patients must be followed up both as MGUS and as hemochromatosis. Copyright 2013 Wiley Periodicals, Inc.[]

  • Biliary Cirrhosis

    Mild eosinophilia (5.9%, 403.9/mmc) occurred 18 months before hospitalization, but all common causes of eosinophilia were excluded.[] […] antibody, present in 90%, is against E2 subunit of pyruvate dehydrogenase complex dihydrolipoamide acetyltransferase on inner face of inner mitochondrial membrane, causes hypocomplementemia[] […] caring for patients with Hepatitis C, Hepatitis B, fatty liver disease, alcoholic liver disease, drug-induced liver disease, genetic and metabolic liver diseases such as Hemochromatosis[]

  • Rapidly Progressive Glomerulonephritis

    Abstract A 61-year-old man developed mononeuritis multiplex accompanied by eosinophilia in 1993.[] The patient was positive for anti-proteinase 3-antineutrophil cytoplasmic antibody (PR3-ANCA) and rheumatoid factor (RF) with hypocomplementemia.[] […] hepatic failure, and cerebral angiitis. ( 25208313 ) Khan T.A....Aggarwal S. 2014 27 Renal hemosiderosis and rapidly progressive glomerulonephritis associated with primary hemochromatosis[]

  • Acquired Cutis Laxa

    An increase of EG2-positive eosinophils in duodenal mucosa associated with elevated serum levels of eosinophil cation protein (ECP) has been documented in psoriatic subjects[] We report a case of γ heavy chain deposition disease (HCDD) associated with acquired cutis laxa, renal involvement, and hypocomplementemia and propose a mechanism of elastic[] Precipitating factors include alcohol ingestion, estrogen administration, certain hepatotoxins (dinitrochlorobenzene, carbon tetrachloride), HIV infection, hemochromatosis[]

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