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2,667 Possible Causes for Hematocrit Decreased, Pancytopenia, Polyclonal Hyperglobulinemia

  • Primary Myelofibrosis

    This is then followed by pancytopenia (a reduction in the number of red and white blood cells, as well as platelets).[] […] the hematocrit, but not the WBC count.[] Polyclonal hyperglobulinemia may be present. Patients with sporadic idiopathic or familial pulmonary hypertension have significant marrow fibrosis.[]

  • Multicentric Castleman's Disease

    hyperglobulinemia, elevated transaminases and renal disease. 2 , 5 , 7 Dispenzieri et al. 8 analyzed the clinical spectrum of Castleman’s disease in 113 patients.[] Diffuse lymph-node enlargement, splenomegaly and pancytopenia were detected. Induction with Rituximab was made because pancytopenia was present.[] Abstract An HIV positive black African woman presented with widespread lymphadenopathy and pancytopenia that had been ascribed to tuberculosis.[]

  • Aplastic Anemia

    Differentiation of AN-associated pancytopenia from other types of pancytopenia, especially idiopathic aplastic anemia (IAA), has not been studied.[] The differential white blood count shows a decrease in most types of cells but not lymphocytes .[] The differential white blood count shows a decrease in most types of cells but not lymphocytes.[]

    Missing: Polyclonal Hyperglobulinemia
  • Pernicious Anemia

    The outcome was rapidly marked by febrile pancytopenia and ataxia leading to the diagnosis of pernicious anemia.[] […] in serum vitamin B 12 and the decline in hematocrit.[] Although her anemia was categorized as "normocytic, normochromic" by an electronic particle counter, evaluation of the pancytopenia confirmed unsuspected pernicious anemia[]

    Missing: Polyclonal Hyperglobulinemia
  • Myelodysplasia

    A 41-year-old patient manifested pancytopenia with macrocytosis following pesticide exposure. She was later found to have myelodysplasia with trisomy 15.[] […] the hematocrit, but not the WBC count.[] Hudspeth and John Lazarchick, Pancytopenia with myelodysplasia due to copper deficiency, Pediatric Blood & Cancer, 51, 5, (693-695), (2008). George J.[]

    Missing: Polyclonal Hyperglobulinemia
  • Systemic Lupus Erythematosus

    A 24-year-old man who had been diagnosed with SLE three months previously, presented with fever, rash, hallucination, and pancytopenia accompanied with hyperferritinemia and[] hematocrit with or without hemoptysis, with diagnosis being confirmed on bronchoalveolar lavage.[] We report the case of a 44-year-old woman admitted with pancytopenia and clinical features of systemic lupus erythematosus, Sjogren's syndrome and antiphospholipid antibodies[]

    Missing: Polyclonal Hyperglobulinemia
  • Multiple Myeloma

    Haematological tests revealed severe anaemia with pancytopenia, which prompted further investigations including a bone marrow biopsy confirming a diagnosis of multiple myeloma[] […] in serum globulin and an increase in hematocrit but no difference in survival compared with a placebo. 36 In another study, prednisone, in a single dose of 200 mg every other[] Marrow function becomes increasingly compromised as patients develop pancytopenia and enter a refractory phase; occasionally, the myeloma cells dedifferentiate and extramedullary[]

    Missing: Polyclonal Hyperglobulinemia
  • Leukemia

    This fact sheet discusses the theory that intermittent fasting may reduce the risk of cancer or improve outcomes with anticancer treatments. more » A 47-Year-Old Woman with Pancytopenia[] Prolonged pancytopenia with severe BM aplasia was seen in a further 2 patients, one of whom died from a fungal pneumonia.[]

    Missing: Polyclonal Hyperglobulinemia
  • Paroxysmal Nocturnal Hemoglobinuria

    We report a 19-year-old female patient admitted to the hospital with pancytopenia. Workout of pancytopenia disclosed paroxysmal nocturnal hemoglobinuria.[] The major causes of associated morbidity and mortality are chronic intravascular hemolysis, pancytopenia, and venous thrombosis.[] Two years after disease onset, while pancytopenia remained stable, occurrence of morning dark urine led to found a paroxysmal nocturnal hemoglobinuria clone.[]

    Missing: Polyclonal Hyperglobulinemia
  • Philadelphia Chromosome Positive Chronic Myeloid Leukemia

    In contrast, IM therapy had no effect on hematocrit in this patient and venesections had to be performed every 6–8 weeks to maintain hematocrit under 48%.[] […] included thrombocytopenia (n 8), diarrhea (n 3), alanine aminotransferase elevation (n 3), aspartate aminotransferase elevation (n 2), dyspnea (n 2), neutropenia (n 2), pancytopenia[] Thus, the progressive decrease in the expression of the Ph-positive clone was associated with an expansion of the JAK2V617F-positive clone, suggesting that IM at a daily dose[]

    Missing: Polyclonal Hyperglobulinemia

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