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199 Possible Causes for Complete Blood Count Abnormal, Erythrocytosis

  • Myeloproliferative Disease

    blood count to examine changes to blood cells, and may also suggest a bone marrow biopsy and aspiration to look for abnormalities.[] 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.[] Blood tests help find abnormal types or numbers of red or white blood cells . They can also detect anemia and leukemia .[]

  • Polycythemia Vera

    A complete blood cell count reveals a hematocrit of 59% with no other abnormalities. A peripheral blood smear is shown in Figure A.[] Unexpectedly, the symptom of erythrocytosis disappeared after the surgery.[] complete blood count (CBC; e.g., Hb 185 g/L in men or 165 g/L in women), but it must be considered in patients with suggestive symptoms.[]

  • Eisenmenger Syndrome

    DIAGNOSTIC TESTING, PHYSICAL FINDINGS, AND ICD-9-CM CODING Diagnostic testing: Diagnostic testing for Eisenmenger syndrome includes: • Complete blood count (CBC); • Chest[] When bunazosin was stopped, the erythrocytosis increased, but when it was resumed, the erythrocytosis and general fatigue diminished.[] […] by specific laboratory investigations; Complete blood count Chest X-ray Cardiac catheterization Echocardiogram Electrocardiogram MRI of heart The management of the disease[]

  • Metastatic Renal Cell Carcinoma

    Another useful lab test is a complete blood count, which includes a count of your red and white blood cell levels. Abnormal levels suggest a possible risk of cancer.[] Tumor cells may produce erythropoietin and provoke erythrocytosis.[] […] 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[]

  • Cyanotic Congenital Heart Disease

    Twin-twin transfusion, IDM Methohemoglobinemia CBC Hb assay ABG: arterial blood gas, AVM: atriovenous malformation, CBC: complete blood count, CNS: central nervous system[] Secondary erythrocytosis of cyanotic congenital heart disease (CCHD) is pathologically different from primary erythrocytosis of polycythemia vera (PV).[] We describe the successful use of hydroxyurea (hydroxycarbamide) in four patients with uncorrected CCHD and symptomatic secondary erythrocytosis.[]

  • Erythrocytosis

    In addition, EPO levels are a very useful tool in recognizing the nature of erythrocytosis.[] […] to an erythrocytosis.[] Patients with chronic interstitial lung disease and erythrocytosis could have normoxemia at rest and a normal or low serum erythropoietin level at the peak of erythrocytosis[]

  • 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[]

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