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259 Possible Causes for Budd-Chiari Syndrome, Erythrocytosis, Polycythemia

  • Myeloproliferative Disease

    Abstract We studied the etiology, diagnosis and natural course of myeloproliferative disease (MPD) in 40 consecutive patients with Budd-Chiari syndrome (BCS).[] Bone marrow fibrosis is also detected in the spent phase of chronic myelogenous leukemia and polycythemia vera. See Workup for more detail.[] 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.[]

  • Polycythemia Vera

    [BuddChiari syndrome (BCS)].[] […] as a primary polycythemia.[] ERYTHROCYTOSIS AND POLYCYTHEMIA VERA 1. In patients with erythrocytosis, which of the following is not characteristic of polycythemia vera?[]

  • Metastatic Renal Cell Carcinoma

    Polycythemia has also been described in mRCC patients. mRCC may be accompanied by amyloidosis, although its pathogenesis remains unclear.[] Paraneoplastic syndromes Around 25% of RCC patients will develop a paraneoplastic syndrome 19-21 : hypercalcemia (20%) hypertension (20%) polycythemia : from erythropoietin[] […] abdominal mass; [9] malaise, which is a general feeling of unwellness; [9] weight loss and/or loss of appetite; [10] anaemia resulting from depression of erythropoietin ; [8] erythrocytosis[]

  • Polycythemia

    syndrome (hepatic vein thrombosis), LFTs should be normal, as the level of the thrombosis is proximal to the liver, and the liver has dual blood supply (hepatic artery) Chronic[] Secondary polycythemia in which the production of erythropoietin increases appropriately is called physiologic polycythemia.[] ERYTHROCYTOSIS AND POLYCYTHEMIA VERA 1. In patients with erythrocytosis, which of the following is not characteristic of polycythemia vera?[]

  • Essential Thrombocythemia

    KEYWORDS: BuddChiari syndrome; essential thrombocythemia; mutation[] IM - Review First Online: 30 September 2009 Abstract The classic myeloproliferative neoplasms (MPNs) include polycythemia vera and essential thrombocythemia; their molecular[] […] at diagnosis and for patients who subsequently develop thrombocytosis, leukocytosis, or erythrocytosis during follow-up, even for CML patients in complete cytogenetic response[]

  • Secondary Polycythemia

    vein thrombosis).[] polycythemia (SP).[] Out of these 53 patients, 28 (53%) patients had PV and 25 (47%) patients had secondary erythrocytosis.[]

  • Stress Polycythemia

    Polycythemia polycythemia Any RBC mass. See Relative polycythemia, Secondary polycythemia.[] ., stroke, Budd-Chiari syndrome) may occur.[] Called also benign or stress erythrocytosis, Gaisbцck disease, pseudopolycythemia, and benign, chronic relative, hypertonic, or spurious p. Medical dictionary. 2011.[]

  • Primary Myelofibrosis

    Of patients with Budd-Chiari syndrome (hepatic-inferior vena cava obstruction), 10% to 13% have coexisting PV; therefore, testing for the presence of JAK2 V617F mutation is[] Megakaryocytes are the "hallmark" of Philadelphia chromosome-negative myeloproliferative neoplasms, such as essential thrombocythemia, polycythemia vera, and primary myelofibrosis[] The laboratory findings showed leuko-and erythrocytosis, increased levels of urea-BUN (32 mmol/l) and creatinine (766 mmol/l) as well as uric acid (920 mmol/l).[]

  • Renal Cell Carcinoma

    Invasion of the IVC may result in the appearance of the BuddChiari syndrome, which causes confusion when checking for metastases.[] After surgery to remove the carcinoma, the secondary polycythemia may resolve.[] In addition, the following may be found: fever, weight loss, anemia, varicocele, and paraneoplastic syndromes (5%) characterized by erythrocytosis, hypercalcemia, liver dysfunction[]

  • Hepatocellular Carcinoma

    […] users of androgenic anabolic steroids They have the following congenital (present at birth) diseases and conditions: Alpha-1 antitrypsin deficiency Ataxia telangiectasia Budd-Chiari[] Another paraneoplastic process is polycythemia due to synthesis of erythopoetin by hepatocytes. What other additional laboratory studies may be ordered?[] Patients with HCC can develop hypoglycemia due to the tumor's high metabolic needs as well as erythrocytosis due to tumor secretion of erythropoietin.[]

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