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423 Possible Causes for Erythrocytosis, Thrombocytosis

  • Paraneoplastic Syndrome

    Lymphoma may be a cause of secondary thrombocytosis. Renal Paraneoplastic Syndrome About 10% patinets with idiopathic nephrotic syndrome have an underlying maligancy.[] Erythrocytosis is common in cancers of the liver, kidney, adrenal glands, lung, thymus, and CNS as well as in gynecologic tumors and myosarcomas.[] […] characterized by typical thrombotic and/or hemorrhagic manifestations, and sometimes leading to thrombocytopenia Thrombocytopenia may also be caused by autoantibodies; the causes of thrombocytosis[]

  • Myeloproliferative Disease

    One patient clearly represents a case of RARS with reactive thrombocytosis.[] These data suggest that erythrocytosis and granulocytosis in JAK2(V617F) mice are the net result of a complex interplay between cell intrinsic and extrinsic factors.[] As controls we considered 61 patients with reactive thrombocytosis referred to our Department in the same period of time.[]

  • Polycythemia Vera

    Objectives: To compare the mutational profiles of patients with primary myelofibrosis (PMF), polycythemia vera (PV), and essential thrombocytosis (ET).[] Unexpectedly, the symptom of erythrocytosis disappeared after the surgery.[] BACKGROUND: Polycythemia vera (PV) and essential thrombocytosis (ET) are hematological disorders characterized by excessive production of mature and functional blood cells[]

  • Polycythemia

    […] and leukocytosis or thrombocytosis, or all three together.[] ERYTHROCYTOSIS AND POLYCYTHEMIA VERA 1. In patients with erythrocytosis, which of the following is not characteristic of polycythemia vera?[] Polycythemia is frequently used synonymously with erythrocytosis; however, polycythemia may imply leukocytosis and thrombocytosis, as well as erythrocytosis.[]

  • Essential Thrombocythemia

    […] primary Thrombocytosis familial thrombocytosis hereditary thrombocythemia hemorrhagic thrombocythemia Primary Thrombocythemia essential thrombocytemia ET essential thrombocytosis[] […] at diagnosis and for patients who subsequently develop thrombocytosis, leukocytosis, or erythrocytosis during follow-up, even for CML patients in complete cytogenetic response[] […] include essential thrombocythemia (ET), polycythemia vera (PV), chronic myeloid leukemia, and primary myelofibrosis (PMF), with the respective features of thrombocytosis, erythrocytosis[]

  • Secondary Polycythemia

    Polycythemia vera, frequently accompanied by thrombocytosis, leukocytosis and enhanced adhesion of blood cells and endothelial cells, have an enhanced risk of thrombosis.[] Out of these 53 patients, 28 (53%) patients had PV and 25 (47%) patients had secondary erythrocytosis.[] Polycythemia vera, for instance, is associated with erythrocytosis, leukocytosis and thrombocytosis.[]

  • Post-Polycythemia Vera Myelofibrosis

    BACKGROUND: The myeloproliferative neoplasms, essential thrombocytosis, polycythemia vera and primary myelofibrosis, share the same acquired genetic lesion, but the concept[] We describe how treatment with a JAK1/2 inhibitor, ruxolitinib, led to the rapid amelioration of marrow fibrosis, erythrocytosis and thrombocytopenia in a 77-year-old man[] Furthermore, in addition to presenting with isolated thrombocytosis, polycythemia vera can present with just erythrocytosis alone, erythrocytosis and splenomegaly, erythrocytosis[]

  • Stress Polycythemia

    ., without leukocytosis, splenomegaly, or thrombocytosis.[] Venesection is often used as the sole treatment and other therapy is reserved to control the thrombocytosis. CHEMOTHERAPY.[] Detection and accurate diagnosis of erythrocytosis is important regardless of its cause.[]

  • Familial Polycythemia

    The mean age at diagnosis, sex predominance, symptoms, and incidence of chromosomal abnormalities, leukocytosis, thrombocytosis, and elevated leukocyte alkaline phosphatase[] In some cases, the cause of erythrocytosis is unknown. Familial erythrocytosis can have different inheritance patterns depending on the gene involved.[] […] a review of benign familial polycythemia—a disease marked by high values for erythrocyte count and hemoglobin, not associated with significant symptoms, leukocytosis or thrombocytosis[]

  • Gaisbock's Syndrome

    Abstract The syndrome of plethora without splenomegaly, leukocytosis, or thrombocytosis was described by Gaisböck in 1905.[] Primary and secondary erythrocytosis show true increase Relative erythrocytosis Hemoconcentration secondary to reduced plasma volume ETIOLOGY/PATHOGENESIS Multifactorial[] […] signs such as: Blood clots Destruction of red blood cells Increased risk for severe infections from bacteria such as Streptococcus pneumoniae and Neisseria meningitidis Thrombocytosis[]

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