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49 Possible Causes for Leukemia, Polychromasia in Peripheral Blood Smear

  • Congenital Dyserythropoietic Anemia Type 1

    The light and electron microscopic appearance of these cells resembled those described in chronic myelogenous leukemia and thalassemia.[] Anisopoikilocytosis with tear-drop forms, polychromasia, basophilic stippling in peripheral blood smear, erythroid hyperplasia with megaloblastoid changes, binucleated cells[] Vives-Corrons JL, Florensa L, Muncunill J, Nomdedeu B, Rozman C (1979) Chronic myelo-monocytic leukemia associated with hereditary pyruvate-kinase deficiency and multiple[]

  • Sideroblastic Anemia

    Abstract Active hairy cell leukemia is associated with an increase of RDW (Red Cell Distribution Width) which normalizes after successful therapy with 2-chlorodeoxyadenosine[] Blood Smear Peripheral blood smear images .[] […] diseases in the Copenhagen series Leukemia 1993 7 : 1975–1986 4.[]

  • Juvenile Myelomonocytic Leukemia

    […] acute myeloid leukemia.[] […] cells on peripheral blood smear ( Figure ).[] Myelomonocytic Leukemia JUVENILE MYELOMONOCYTIC LEUKEMIA; JMML Juvenile Chronic Myelogenous Leukemia JCML Leukemia, Chronic Myelomonocytic Leukemia, Juvenile Myelomonocytic[]

  • Pancytopenia

    We report a case of recurrent pancytopenia resulting from maintenance chemotherapy in a patient with acute promyelocytic leukemia and two pharmacogenetic mutations, namely[] blood smear examination for which Leishman stain was used.[] Abstract A small group of children with acute lymphoblastic leukemia (ALL) have a preleukemic phase of pancytopenia followed by a period of spontaneous remission before the[]

  • Secondary Myelofibrosis

    METHODS: Seventeen patients with chronic myelogenous leukemia and 3 with idiopathic polycythaemia presented with splenomegaly, splenic pain and anemia.[] The peripheral smear of patients with primary myelofibrosis includes red blood cells of variable shape (including tear drop cells) and size and variable degrees of polychromasia[] RESULTS: The post-MPN MF cases included chronic myeloid leukemia-MF and polycythemia vera-MF.[]

  • Acquired Sideroblastic Anemia

    […] or Acute Lymphocytic Leukemia Completed NCT00462605 Phase 2 entinostat;sargramostim 21 Thalidomide in Treating Patients With Myelodysplastic Syndrome Completed NCT00015990[] Blood Smear Peripheral blood smear images .[] The patient was followed for 45 months and no signs of chronic myeloid leukemia or other leukemic transformation developed. In IASA the chromosomal changes are variable.[]

  • Chronic Acquired Pure Red Cell Aplasia

    ", keywords "Alemtuzumab, Chronic lymphocytic leukemia, Pure red cell aplasia, Rituximab, Therapy", author "Giovanni D'Arena and N.[] blood smear showed anisocytosis, poikilocytosis, polychromasia and leukocytosis.[] Rituximab-cyclophosphamide-dexamethasone combination in the management of autoimmune cytopenias associated with chronic lymphocytic leukemia. Leukemia. 2011;25:473-8.[]

  • Autoimmune Hemolytic Anemia

    Abstract Ibrutinib (IBR) covalently binds to the active site of Bruton's tyrosine kinase (BTK) and is used for the treatment of relapsed/refractory chronic lymphocytic leukemia[] Peripheral blood smear showed polychromasia and spherocytosis. Haptoglobin level was 0.06 g/L ( N 0.16-2). Both hemoglobin electrophoresis and G6PD level were normal.[] Red blood cell agglutination, polychromasia, target cells and spherocytes were seen on a peripheral smear.[]

  • Hemolytic Anemia

    Autoimmune hemolytic anemia can occur in patients who have chronic lymphocytic leukemia (cll).[] Mean corpuscular volume was 96 fl, and the reticulocyte count was 11%, with marked polychromasia on peripheral smear.[] Bone marrow transplants or stem cell transplants may be an option for children with: Acute lymphoblastic leukemia (ALL) that has relapsed (responded initially to treatment[]

  • Cold Agglutinin Disease

    Abstract Autoimmune phenomena may precede or accompany lymphoid malignancies, especially B-chronic lymphocytic leukemia (B-CLL).[] Reticulocytes and Spherocytes The results of the reticulocyte count are usually increased in patients with cold agglutinin disease, with polychromasia in the peripheral blood[] Other laboratory findings include reticulocytosis, positive DAT, auto agglutination and/or rouleaux on peripheral blood smear, polychromasia, and mild to moderate anisocytosis[]

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