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65 Possible Causes for Erythrocytosis, Malar Rash

  • Myeloproliferative Disease

    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.[] Our data seem to indicate that both thrombocytosis and erythrocytosis resembled primary forms in these subjects; however, none of them suffered serious thrombotic and/or hemorrhagic[] Somatic Mutations of JAK2 Exon 12 in Patients with Polycythemia Vera or Idiopathic Erythrocytosis.[]

  • Polycythemia Vera

    Unexpectedly, the symptom of erythrocytosis disappeared after the surgery.[] ERYTHROCYTOSIS AND POLYCYTHEMIA VERA 1. In patients with erythrocytosis, which of the following is not characteristic of polycythemia vera?[] We report a case of erythrocytosis as the primary manifestation of a chronic myeloid leukemia, with the presence of the Philadelphia chromosome and the Breakpoint cluster[]

  • Secondary Polycythemia

    Out of these 53 patients, 28 (53%) patients had PV and 25 (47%) patients had secondary erythrocytosis.[] This is most likely due to the worse prognosis associated with the underlying disease causing erythrocytosis.[] At the same time, scientific literature is lacking in data about patients with secondary erythrocytosis and CVA.[]

  • Stress Polycythemia

    Called also benign or stress erythrocytosis, Gaisbцck disease, pseudopolycythemia, and benign, chronic relative, hypertonic, or spurious p. Medical dictionary. 2011.[] Detection and accurate diagnosis of erythrocytosis is important regardless of its cause.[] Synonym: erythrocytosis Chuvash polycythemia An autosomal recessive erythrocytosis in which patients respond to normal oxygen levels as if they were in an hypoxic environment[]

  • Polycythemia Neonatorum

    […] conjunctivitis Inclusion: Ophthalmia neonatorum due to gonococcus D45 Polycythemia vera excludes: familial polycythemia (D75.0) secondary polycythemia (D75.1) D75.0 Familial erythrocytosis[] : D75.1 , R71 ICD-10-CM Diagnosis Code D75.1 Secondary polycythemia 2016 2017 2018 2019 Billable/Specific Code Applicable To Acquired polycythemia Emotional polycythemia Erythrocytosis[] H Nagy K, Pomucz J, Varga R, Szabó E, Soltész G Erythrocytosis and severe asphyxia: two different causes of neonatal myocardial infarction.[]

  • Familial Polycythemia

    In some cases, the cause of erythrocytosis is unknown. Familial erythrocytosis can have different inheritance patterns depending on the gene involved.[] Adamson JW et al. (1973) Recessive familial erythrocytosis: aspects of marrow regulation in two families. [ ] 18. Davey MG et al. (1968) Femilial erythrocytosis.[] erythrocytosis, androgen therapy, Cushing's disease, truncation of EPOR and hypertransfusion, in addition to the familial erythrocytosis and idiopathic erythrocytosis. [6[]

  • Carcinoid Tumor

    […] less than 10% of the cases); then, the following may be noted: Increased blood pressure (hypertension) Increased calcium in blood (hypercalcemia) Increased red blood cells (erythrocytosis[]

  • Dermatomyositis

    12 (44.4%) Malar rash 14 (51.9%) Gottron’s sign 23 (85.2%) V Sign 16 (59.3%) Shawl Sign 15 (55.6%) Nail-bed erythema 17 (63.0%) Dilated capillary loops 14 (51.9%) Holster[] Dermatomyositis and erythrocytosis associated with hepatocellular carcinoma. J Gastroenterol Hepatol. 2002;17(11):1239-40.[] ; there can also be redness over the cheeks (malar rash) as well as on other parts of the body (top of the knuckles, knees and elbows) where the skin can become thickened[]

  • Malignant Carcinoid Syndrome

    Due to prolonged vasodilation, purplish rash (usually on the nose, upper lip, and malar area) tend to appear at the late stage of carcinoid syndrome.[] Erythrocytosis is common in regions of the liver, kidney, adrenal glands, lung, thymus, and central nervous system (as well as gynecological tumors and myosarcomas ). [7][]

  • Hemolytic Anemia

    rash and/or arthritis might suggest systemic lupus erythematosus A history of chronic sinorespiratory infections could indicate common variable immunodeficiency Reticulocyte[] Intrinsic hemolytic anemias are often inherited, such as sickle cell anemia, thalassemia, or erythrocytosis.[] It includes sickle cell anemia, thalassemia, or erythrocytosis. These conditions produce red blood cells that don't live as long as normal red blood cells. Extrinsic.[]

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