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SUMMATIVE EXAM #4

SUMMATIVE EXAM #4
100問 • 1年前
  • Yves Laure Pimentel
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    問題一覧

  • 1

    Which parameters are calculated rather than directly measured? A. Hematocrit and erythrocyte distribution width B. Erythrocyte count and leukocyte count C. Leukocyte count and hematocrit D. Platelet count and platelet volume

    A. Hematocrit and erythrocyte distribution width

  • 2

    If the RBC distribution on histogram demonstrates a homogenous pattern and small SD, the peripheral blood smear would probably exhibit: A. Extreme anisocytosis B. Very little anisocytosis C. A single population of spherocytes D. A single population of macrocytes

    B. Very little anisocytosis

  • 3

    The RDW and MCV are both quantitative descriptors of erythrocyte size. If both are increased, the most probable erythrocytic abnormality would be: A. Iron deficiency anemia B. Acquired aplastic anemia C. Megaloblastic anemia D. Hemoglobinopathy

    C. Megaloblastic anemia

  • 4

    In an erythrocyte histogram, the erythrocytes that are larger than normal will be to the ____ of the normal distribution curve. A. Right B. Left C. Middle D. Variable

    A. Right

  • 5

    RL flag except: A. Platelet clumps B. RBC fragments C. Giant platelets D. Cold agglutinins

    D. Cold agglutinins

  • 6

    Mean platelet volume (MPV): A. Analogous to MCHC B. Direct measure of platelet count C. Measurement of the average volume of platelets D. Comparison of the patient’s value to the normal value

    C. Measurement of the average volume of platelets

  • 7

    The MPV is often decreased in: A. Sickle cell anemia B. Megaloblastic anemia C. Idiopathic thrombocytopenic purpura D. After splenectomy

    B. Megaloblastic anemia

  • 8

    Normal PDW: A. Less than 5% B. Less than 10% C. Less than 15% D. Less than 20%

    D. Less than 20%

  • 9

    Which cell surface membrane marker is used for enumeration of HPC enumeration? HEMATOPOIETIC PROGENITOR CELLS A. CD 4 B. CD 8 C. CD 34 D. CD 45

    C. CD 34

  • 10

    The normal sequence of blood cell development is: A. Yolk sac—red bone marrow—liver and spleen B. Yolk sac—thymus—liver and spleen—red bone marrow C. Yolk sac—liver and spleen—red bone marrow D. Liver and spleen—yolk sac—red bone marrow

    C. Yolk sac—liver and spleen—red bone marrow

  • 11

    The abbreviation MAPCs stands for: A. Multiple adult progenitor cells B. Multipotent adult progenitor cells C. Many abnormal progenitor cells D. Multiply active potential cells

    B. Multipotent adult progenitor cells

  • 12

    The best source of active bone marrow from a 20- year-old would be: A. Iliac crest B. Femur C. Distal radius D. Tibia

    A. Iliac crest

  • 13

    Primary target cells of G-CSF, EXCEPT: A. Fibroblasts B. Leukemic myeloblasts C. Neutrophil precursors D. T and B cells

    D. T and B cells

  • 14

    Bone marrow cellularity refers to the ratio of: A. Red cell precursors to white cell precursors B. Hematopoietic tissue to adipose tissue C. Granulocytic cells to erythrocytic cells D. Extravascular tissue to intravascular tissue

    B. Hematopoietic tissue to adipose tissue

  • 15

    The maturational sequence(s) of the erythrocyte is (are): A. Rubriblast—prorubricyte—metarubricyte— rubricyte—reticulocyte—mature erythrocyte B. Rubriblast—prorubricyte—rubricyte— metarubricyte—reticulocyte—mature erythrocyte C. Pronormoblast—basophilic normoblast—polychromatophilic normoblast—orthochromic normoblast—reticulocyte—mature erythrocyte D. Both B and C

    D. Both B and C

  • 16

    The cell maturation sequence of the segmented neutrophil is: A. Promyelocyte—myeloblast—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN) B. Myeloblast—promyelocyte—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN) C. Monoblast—promyelocyte—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN) D. Promyelocyte—myelocyte—metamyelocyte— band or stab—segmented neutrophil (PMN)

    B. Myeloblast—promyelocyte—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN)

  • 17

    The maturational sequence of the thrombocyte (platelet) is: A. Megakaryoblast—promegakaryocyte— megakaryocyte—metamegakaryocyte— thrombocyte B. Promegakaryocyte—megakaryocyte— metamegakaryocyte—thrombocyte C. Megakaryoblast—promegakaryocyte— megakaryocyte—thrombocyte D. Megakaryoblast—promegakaryocyte— metamegakaryocyte—thrombocyte

    C. Megakaryoblast—promegakaryocyte— megakaryocyte—thrombocyte

  • 18

    As a blood cell matures, the overall cell diameter in most cases: A. Increases B. Decreases C. Remains the same D. Variable

    B. Decreases

  • 19

    As a blood cell matures, the ratio of nucleus to cytoplasm (N:C) in most case: A. Increases B. Decreases C. Remains the same D. Variable

    B. Decreases

  • 20

    The chromatin pattern, in most cells, as the cell matures: A. Becomes more clumped B. Becomes less clumped C. Remains the same D. Variable

    A. Becomes more clumped

  • 21

    IN GENERAL, cytoplasmic color in younger cells: A. Pink B. Red C. Dark blue D. Light blue

    C. Dark blue

  • 22

    In the blast stage of DEVELOPMENT OF LEUKOCYTES, the cytoplasm of the cell is: A. Dark blue and lacks vacuoles B. Light blue and lacks granules C. Light blue and has specific granules D. Gray with many dark-blue granules

    B. Light blue and lacks granules

  • 23

    Hemoglobin appears for the first time in the ____ maturational stage of erythrocytes. A. Second B. Third C. Fourth D. Fifth

    B. Third

  • 24

    Which is the first stage of erythrocytic maturation in which the cytoplasm is pink due to the formation of hemoglobin? A. Reticulocyte B. Pronormoblast C. Basophilic normoblast D. Polychromatic normoblast

    D. Polychromatic normoblast

  • 25

    With a normal diet, an erythrocyte remains in the reticulocyte stage in the circulating blood for: A. 1 day B. 2.5 days C. 3 days D. 120 days

    A. 1 day

  • 26

    In a Wright-stained peripheral blood film, the reticulocyte will have a blue appearance. This is referred to as: A. Megaloblastic maturation B. Bluemia C. Polychromatophilia D. Erythroblastosis

    C. Polychromatophilia

  • 27

    The types of granulocytic leukocytes found in the proliferative compartment of the bone marrow are: A. Myeloblasts, myelocyte and metamyelocytes B. Myeloblasts, promyelocytes and metamyelocytes C. Myeloblasts, promyelocytes, myelocytes and metamyelocytes D. Myeloblasts, promyelocytes, myelocytes, metamyelocytes and band neutrophils

    C. Myeloblasts, promyelocytes, myelocytes and metamyelocytes

  • 28

    The types of granulocytic leukocytes found in the maturation-storage compartment of the bone marrow are: A. Metamyelocytes, band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils B. Only band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils C. Metamyelocytes, band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils D. Segmented neutrophils, immature and mature monocytes and mature lymphocytes

    A. Metamyelocytes, band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils

  • 29

    Identify the cell with these characteristics: prominent primary granules that are rich in myeloperoxidase and chloroacetate esterase and have a diameter of 14 to 20 µm. A. Myeloblast B. Promyelocyte C. Myelocyte D. Promonocyte

    B. Promyelocyte

  • 30

    The earliest granulocytic maturational stage in which secondary or specific granules appear is: A. Myeloblast B. Monoblast C. Promyelocyte D. Myelocyte

    D. Myelocyte

  • 31

    The most mature granulocyte precursor that can undergo mitosis is the: A. Myeloblast B. Promyelocyte C. Myelocyte D. Metamyelocyte

    C. Myelocyte

  • 32

    Which of the following can differentiate metamyelocytes from other stages of granulocyte maturation? A. Presence of specific granules B. Indentation of nucleus C. Absence of nucleoli D. Color of cytoplasm

    B. Indentation of nucleus

  • 33

    The stage in neutrophilic development in which the nucleus is indented in a kidney bean shape and the cytoplasm has secondary granules that are lavender in color is the: A. Band B. Myelocyte C. Promyelocyte D. Metamyelocyte

    D. Metamyelocyte

  • 34

    Which of the following are contents of basophilic granules? A. Heparin B. Histamine C. Myeloperoxidase D. Both A and B

    D. Both A and B

  • 35

    The half-life of circulating granulocytes in the blood is estimated to be: A. 2.5 to 5 hours B. 7 to 10 hours C. 24 hours D. 2 days

    B. 7 to 10 hours

  • 36

    A characteristic of a segmented neutrophil is: A. Large orange granules B. An elongated and curved nucleus C. Light sky-blue cytoplasm D. Greatest number of WBCs in the peripheral blood of an adult

    D. Greatest number of WBCs in the peripheral blood of an adult

  • 37

    A characteristic of mature eosinophil is: A. Large orange granules B. Elongated and curved nucleus C. Light, sky-blue cytoplasm D. Kidney bean-shaped nucleus

    A. Large orange granules

  • 38

    A characteristic of mature monocyte: A. Large orange granules B. Elongated and curved nucleus C. Light, sky-blue cytoplasm D. Kidney bean-shaped nucleus

    D. Kidney bean-shaped nucleus

  • 39

    A characteristic of mature lymphocyte is: A. Large, orange granules B. Elongated and curved cytoplasm C. Light, sky-blue cytoplasm D. Kidney bean-shaped nucleus

    C. Light, sky-blue cytoplasm

  • 40

    An increase in metamyelocytes, myelocytes and promyelocytes can be referred to as: A. Leukocytopenia B. Shift to the right C. Shift to the left D. Pelger-Huet anomaly

    C. Shift to the left

  • 41

    The major function of the neutrophilic granulocytes: A. Antibody production B. Destruction of parasites C. Phagocytosis D. Suppression of inflammation

    C. Phagocytosis

  • 42

    The principal leukocyte type involved in phagocytosis: A. Monocyte B. Neutrophil C. Eosinophil D. Basophil

    B. Neutrophil

  • 43

    The major function of eosinophil is: A. Suppression of inflammatory reactions B. Destruction of protozoa C. Participation in anaphylaxis D. Phagocytosis

    A. Suppression of inflammatory reactions

  • 44

    Which of the following is/are characteristic/s of erythropoietin? A. Glycoprotein B. Secreted by the liver C. Secreted by the kidneys D. All of the above

    D. All of the above

  • 45

    Stimulation of erythropoietin is caused by: A. Tissue hypoxia B. Hypervolemia C. Inflammation D. Infection

    A. Tissue hypoxia

  • 46

    Biochemical abnormalities characteristic of polycythemia vera include: A. Increased serum B12 binding capacity B. Hypohistaminemia C. Hypouricemia D. Decreased leukocyte alkaline phosphatase activity

    A. Increased serum B12 binding capacity

  • 47

    Increased erythropoietin production in secondary polycythemia can be caused by: A. Chronic lung disease B. Smoking C. Renal neoplasms D. All of the above

    D. All of the above

  • 48

    Relative polycythemia exists when: A. Increased erythropoietin is produced B. Total blood volume is expanded C. Plasma volume is increased D. Plasma volume is decreased

    D. Plasma volume is decreased

  • 49

    The primary pathophysiologic mechanism of anemia associated with chronic kidney disease is: A. Inadequate production of erythropoietin B. Excessive hemolysis C. Hematopoietic stem cell mutation D. Toxic destruction of stem cells

    A. Inadequate production of erythropoietin

  • 50

    D. Toxic destruction of stem cells 650. Effect of increased amounts of 2,3-DPG to oxygen affinity of the hemoglobin molecule. A. Increases B. Decreases C. Do not alter D. Variable

    B. Decreases

  • 51

    The most common erythrocytic enzyme deficiency involving the Embden-Meyerhof glycolytic pathway is a deficiency of: A. ATPase B. Pyruvate kinase C. Glucose-6-phosphate dehydrogenase D. Lactic dehydrogenase

    B. Pyruvate kinase

  • 52

    The final steps in heme synthesis, including the formation of protoporphyrin take place in: A. Cell’s nucleus B. Cell’s cytoplasm C. Spleen D. Mitochondria

    D. Mitochondria

  • 53

    In an alkaline pH (pH of 8.6) electrophoresis is performed, hemoglobin E has the same mobility as hemoglobin: A. S B. F C. A D. C

    D. C

  • 54

    The type of hemoglobin that is detectable with the Kleihauer-Betke test is: A. A B. A2 C. F D. S

    C. F

  • 55

    f female patient is diagnosed with anemia and her follow-up assays indicated blood serum results of increased bilirubin and decreased haptoglobin and hemosiderin in her urinary sediment, what is the most probable diagnosis? A. Extravascular catabolism B. Intravascular catabolism C. Defective hemoglobin synthesis D. Thalassemia

    B. Intravascular catabolism

  • 56

    If you are grading changes in erythrocytic size or shape using a scale of 0 to 4+ and MANY erythrocytes deviate from normal per microscopic field, the typical score would be A. 1+ B. 2+ C. 3+ D. 4+

    C. 3+

  • 57

    Which of the following is associated with a defect in nuclear maturation? A. Microcytes B. Sickle cells C. Megalocytes D. Acanthocytes

    C. Megalocytes

  • 58

    Which of the following represents an imbalance between erythrocytic and plasma lipids? A. Microcytes B. Sickle cells C. Macrocytes D. Acanthocytes

    D. Acanthocytes

  • 59

    Acanthocytes may be associated with the clinical condition of: A. Iron deficiency anemia B. Abetalipoproteinemia C. Pernicious anemia D. No related disease state

    B. Abetalipoproteinemia

  • 60

    Spherocytes: A. Short, scalloped, or spike-like projections that are regularly distributed around the cell B. Fragments of erythrocytes C. The scooped-out part of an erythrocyte that remains after a blister cell ruptures D. Compact round shape

    D. Compact round shape

  • 61

    Dacryocytes may be seen in: A. Hepatic disorders B. Hemolytic disease of the fetus and newborn C. Hemoglobinopathies D. Pernicious anemia

    D. Pernicious anemia

  • 62

    Basophilic stippling represents: A. DNA B. Precipitated denatured hemoglobin C. Granules of ribosomes and RNA D. Aggregates of iron, mitochondria and ribosomes

    C. Granules of ribosomes and RNA

  • 63

    Pappenheimer bodies represent: A. DNA B. Precipitated denatured hemoglobin C. Granules of ribosomes and RNA D. Aggregates of iron, mitochondria and ribosomes

    D. Aggregates of iron, mitochondria and ribosomes

  • 64

    Fanconi’s anemia is associated with abnormal genes located on chromosomes: A. 9, 20 B. 5, 22 C. 9, 12 D. 8, 23

    A. 9, 20

  • 65

    The average adult has ____g of total iron. A. 0.2 to 1.4 B. 1.5 to 3.4 C. 3.5 to 5.0 D. 5.1 to 10.0

    C. 3.5 to 5.0

  • 66

    The cytochemical stain that can demonstrate iron, hemosiderin and ferritin is: A. New methylene blue B. Romanowsky C. Prussian blue D. Wright-Giemsa

    C. Prussian blue

  • 67

    I What is the major metabolically available storage form of iron in the body? A. Hemosiderin B. Ferritin C. Transferrin D. Hemoglobin

    B. Ferritin

  • 68

    The total iron-binding capacity (TIBC) of the serum is an indirect measure of which iron-related protein? A. Hemosiderin B. Ferritin C. Transferrin D. Hemoglobin

    C. Transferrin

  • 69

    The transfer of iron from the enterocyte into the plasma is REGULATED by: A. Transferrin B. Ferroportin C. Hephaestin D. Hepcidin

    D. Hepcidin

  • 70

    In stage 3 IDA, the erythrocyte indices are typically: A. MCV increased, MCH decreased, and MCHC decreased B. MCV decreased, MCH decreased, and MCHC decreased C. MCV decreased, MCH increased, and MCHC decreased D. MCV decreased, MCH decreased, and MCHC normal

    B. MCV decreased, MCH decreased, and MCHC decreased

  • 71

    In megaloblastic anemia, the typical erythrocytic indices are: A. MCV increased, MCH increased, and MCHC normal B. MCV increased, MCH variable, and MCHC normal C. MCV increased, MCH decreased, and MCHC normal D. MCV normal, MCH increased, and MCHC norma

    A. MCV increased, MCH increased, and MCHC normal

  • 72

    Which of the following can be found in a patient with classic megaloblastic anemia? A. Ovalocytes and hypersegmented neutrophils B. Hypochromic macrocytes and variant lymphocytes C. Howell-Jolly bodies and Pappenheimer bodies D. Lymphocytosis

    A. Ovalocytes and hypersegmented neutrophils

  • 73

    n cold-type AIHA: A. IgM, usually anti-I is present B. Rh antibodies are the most frequent cause C. IgM usually occurs in newborn infants D. Autoantibodies are present

    A. IgM, usually anti-I is present

  • 74

    Which of the following is NOT associated with hemolytic anemia? A. Decrease hemoglobin and packed cell volume B. Increased reticulocyte count C. Increased serum haptoglobin D. Decreased erythrocyte survival

    C. Increased serum haptoglobin

  • 75

    Paroxysmal nocturnal hemoglobinuria exhibits sensitivity of one population of red cells to: A. Warm antibodies B. Cold antibodies C. Complement D. Either A and B

    C. Complement

  • 76

    The defect in PNH is a/an ____ associated defect of the RBC membrane. A. Structural protein B. Hemoglobin C. Antibody D. Enzyme

    A. Structural protein

  • 77

    What factors contribute to the sickling of erythrocytes in sickle cell disease crisis? A. Increase in blood pH and increase in oxygen B. Extremely hot weather C. Extremely reduced oxygen and increased acidity in the blood D. Sickling is spontaneous

    C. Extremely reduced oxygen and increased acidity in the blood

  • 78

    Lymphocyte development in the thymus and bursal equivalent are: A. Antigen-independent B. Antigen-dependent C. Antibody-independent D. Antibody-dependent

    A. Antigen-independent

  • 79

    Which of the following is characteristic of Dohle body inclusions? A. Gigantic peroxidase positive deposits B. Precipitated mucopolysaccharides C. Dark blue cytoplasmic inclusions D. Single or multiple pale-blue staining inclusions

    D. Single or multiple pale-blue staining inclusions

  • 80

    Which of the following is characteristic of MayHegglin anomaly? A. Gigantic peroxidase-positive deposits B. Precipitated mucopolysaccharides C. Dohle body-like inclusions and giant platelets D. Single or multiple pale blue staining inclusions

    C. Dohle body-like inclusions and giant platelets

  • 81

    Cytoplasmic inclusion in Alder-Reilly anomaly can resemble: A. Dohle bodies B. Toxic granulation C. Auer rods D. Parasites

    B. Toxic granulation

  • 82

    azy leukocyte syndrome is associated with the: A. Neutrophilic series B. Monocytic-macrophage series C. Lymphocytic series D. Erythrocytic series

    A. Neutrophilic series

  • 83

    Smudge cells are associated with: A. Niemann Pick disease and Burkitt’s lymphoma B. CLL C. Leukosarcoma D. Natural artifact

    B. CLL

  • 84

    The EBV infects: A. T cells B. B cells C. Monocytes D. Macrophages

    B. B cells

  • 85

    Multiple myeloma is a disorder of: A. T lymphocytes B. Megakaryocytes C. Plasma cells D. Lymph notes

    C. Plasma cells

  • 86

    WM is characterized by increased levels of: A. IgG B. IgM C. IgD D. IgA

    B. IgM

  • 87

    According to the WHO classification, except in leukemias with specific genetic anomalies, the minimal percentage of blasts necessary for a diagnosis of acute leukemia is: A. 10% B. 20% C. 30% D. 50%

    B. 20%

  • 88

    Acute leukemia can be described as being: A. Short duration with many mature leukocyte forms in the peripheral blood B. Short duration with many immature leukocyte forms in the peripheral blood C. Short duration with little alteration of the leukocytes of the peripheral blood D. Long duration with many mature leukocyte forms in the peripheral blood

    B. Short duration with many immature leukocyte forms in the peripheral blood

  • 89

    Myeloid without maturation acute leukemias is classified as: A. M1 B. M4 C. M5 D. L1

    A. M1

  • 90

    Myeloblasts, promyelocytes and myelocytes predominate in: A. M2 B. M3 C. M4 D. M6

    A. M2

  • 91

    Many coarsely granular promyelocytes with dumbbell-shaped or bilobed nuclei predominate in: A. M2 B. M3 C. M4 D. M6

    B. M3

  • 92

    Myeloid and monocytic acute leukemias are classified as FAB: A. M1 B. M4 C. M5 D. L1

    B. M4

  • 93

    Monocytic acute leukemia is classified as FAB: A. M1 B. M4 C. M5 D. L1

    C. M5

  • 94

    Immature leukocytic and erythrocytic cell types predominate in: A. M2 B. M3 C. M4 D. M6

    D. M6

  • 95

    Chloromas are associated with: A. FAB M1 B. FAB M3 C. FAB M4 D. FAB M5

    A. FAB M1

  • 96

    Myeloperoxidase (MPO) and Sudan Black B (SBB) staining results: A. Opposite B. Parallel C. Undetermined D. Variable

    B. Parallel

  • 97

    Which cell type demonstrates the most intense peroxidase reaction? A. Neutrophil B. Basophil C. Lymphocyte D. Monocyte

    A. Neutrophil

  • 98

    Cells do not exhibit myeloperoxidase (MPO) activity: A. Eosinophils B. Neutrophils C. Lymphocytes D. Monocytes

    C. Lymphocytes

  • 99

    Detects lymphocytic cells and certain abnormal ERYTHROCYTIC CELLS by staining of cytoplasmic GLYCOGEN: A. MPO B. SBB C. PAS D. Tdt

    C. PAS

  • 100

    A laboratory assay that can be used to differentiate a leukemoid reaction from chronic myelogenous leukemia is: A. Leukocyte alkaline phosphatase (LAP) stain B. Erythrocyte sedimentation rate (ESR) C. Assessment of the shift to the left D. Absolute neutrophil count

    A. Leukocyte alkaline phosphatase (LAP) stain

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    43問 • 1年前
    Yves Laure Pimentel

    CC- CARBOHYDRATES

    CC- CARBOHYDRATES

    Yves Laure Pimentel · 49問 · 2年前

    CC- CARBOHYDRATES

    CC- CARBOHYDRATES

    49問 • 2年前
    Yves Laure Pimentel

    CC- DIABETES MELLITUS

    CC- DIABETES MELLITUS

    Yves Laure Pimentel · 97問 · 2年前

    CC- DIABETES MELLITUS

    CC- DIABETES MELLITUS

    97問 • 2年前
    Yves Laure Pimentel

    MAJOR LIPOPROTEINS

    MAJOR LIPOPROTEINS

    Yves Laure Pimentel · 57問 · 2年前

    MAJOR LIPOPROTEINS

    MAJOR LIPOPROTEINS

    57問 • 2年前
    Yves Laure Pimentel

    MINOR LIPOPROTEINS

    MINOR LIPOPROTEINS

    Yves Laure Pimentel · 63問 · 2年前

    MINOR LIPOPROTEINS

    MINOR LIPOPROTEINS

    63問 • 2年前
    Yves Laure Pimentel

    PROTEINS

    PROTEINS

    Yves Laure Pimentel · 37問 · 2年前

    PROTEINS

    PROTEINS

    37問 • 2年前
    Yves Laure Pimentel

    PLASMA PROTEINS 1

    PLASMA PROTEINS 1

    Yves Laure Pimentel · 91問 · 2年前

    PLASMA PROTEINS 1

    PLASMA PROTEINS 1

    91問 • 2年前
    Yves Laure Pimentel

    PLASMA PROTEINS 2 (ALPHA 2 REGION)

    PLASMA PROTEINS 2 (ALPHA 2 REGION)

    Yves Laure Pimentel · 98問 · 2年前

    PLASMA PROTEINS 2 (ALPHA 2 REGION)

    PLASMA PROTEINS 2 (ALPHA 2 REGION)

    98問 • 2年前
    Yves Laure Pimentel

    MISCELLANEOUS PROTEINS

    MISCELLANEOUS PROTEINS

    Yves Laure Pimentel · 61問 · 2年前

    MISCELLANEOUS PROTEINS

    MISCELLANEOUS PROTEINS

    61問 • 2年前
    Yves Laure Pimentel

    Liver Function Test 1

    Liver Function Test 1

    Yves Laure Pimentel · 100問 · 2年前

    Liver Function Test 1

    Liver Function Test 1

    100問 • 2年前
    Yves Laure Pimentel

    Liver Function Test 2

    Liver Function Test 2

    Yves Laure Pimentel · 96問 · 2年前

    Liver Function Test 2

    Liver Function Test 2

    96問 • 2年前
    Yves Laure Pimentel

    TUMOR MARKERS

    TUMOR MARKERS

    Yves Laure Pimentel · 33問 · 2年前

    TUMOR MARKERS

    TUMOR MARKERS

    33問 • 2年前
    Yves Laure Pimentel

    KIDNEY FUNCTION TESTS - NON PROTEIN NITROGEN & CREATININE

    KIDNEY FUNCTION TESTS - NON PROTEIN NITROGEN & CREATININE

    Yves Laure Pimentel · 41問 · 2年前

    KIDNEY FUNCTION TESTS - NON PROTEIN NITROGEN & CREATININE

    KIDNEY FUNCTION TESTS - NON PROTEIN NITROGEN & CREATININE

    41問 • 2年前
    Yves Laure Pimentel

    GLYCOGEN STORAGE DISEASES

    GLYCOGEN STORAGE DISEASES

    Yves Laure Pimentel · 17問 · 2年前

    GLYCOGEN STORAGE DISEASES

    GLYCOGEN STORAGE DISEASES

    17問 • 2年前
    Yves Laure Pimentel

    LIPID STORAGE DISEASES

    LIPID STORAGE DISEASES

    Yves Laure Pimentel · 14問 · 2年前

    LIPID STORAGE DISEASES

    LIPID STORAGE DISEASES

    14問 • 2年前
    Yves Laure Pimentel

    PROTEINS

    PROTEINS

    Yves Laure Pimentel · 71問 · 2年前

    PROTEINS

    PROTEINS

    71問 • 2年前
    Yves Laure Pimentel

    QUICK FIRE- ELECTRODES

    QUICK FIRE- ELECTRODES

    Yves Laure Pimentel · 7問 · 2年前

    QUICK FIRE- ELECTRODES

    QUICK FIRE- ELECTRODES

    7問 • 2年前
    Yves Laure Pimentel

    ELECTROLYTES

    ELECTROLYTES

    Yves Laure Pimentel · 10問 · 2年前

    ELECTROLYTES

    ELECTROLYTES

    10問 • 2年前
    Yves Laure Pimentel

    DRUGS

    DRUGS

    Yves Laure Pimentel · 27問 · 2年前

    DRUGS

    DRUGS

    27問 • 2年前
    Yves Laure Pimentel

    TOXIC AGENTS:

    TOXIC AGENTS:

    Yves Laure Pimentel · 12問 · 2年前

    TOXIC AGENTS:

    TOXIC AGENTS:

    12問 • 2年前
    Yves Laure Pimentel

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    Yves Laure Pimentel · 100問 · 2年前

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    HEMATOLOGY 1 (HEMATOPOIESIS 1)

    100問 • 2年前
    Yves Laure Pimentel

    HEMATOLOGY (HEMATOPOIESIS 2)

    HEMATOLOGY (HEMATOPOIESIS 2)

    Yves Laure Pimentel · 29問 · 2年前

    HEMATOLOGY (HEMATOPOIESIS 2)

    HEMATOLOGY (HEMATOPOIESIS 2)

    29問 • 2年前
    Yves Laure Pimentel

    hema diseases

    hema diseases

    Yves Laure Pimentel · 25問 · 2年前

    hema diseases

    hema diseases

    25問 • 2年前
    Yves Laure Pimentel

    AML

    AML

    Yves Laure Pimentel · 43問 · 2年前

    AML

    AML

    43問 • 2年前
    Yves Laure Pimentel

    GLOBIN SYNTHESIS

    GLOBIN SYNTHESIS

    Yves Laure Pimentel · 71問 · 2年前

    GLOBIN SYNTHESIS

    GLOBIN SYNTHESIS

    71問 • 2年前
    Yves Laure Pimentel

    HEMATOLOGY REFERENCE RANGES

    HEMATOLOGY REFERENCE RANGES

    Yves Laure Pimentel · 31問 · 2年前

    HEMATOLOGY REFERENCE RANGES

    HEMATOLOGY REFERENCE RANGES

    31問 • 2年前
    Yves Laure Pimentel

    DISORDERS OF PRIMARY HEMOSTASIS

    DISORDERS OF PRIMARY HEMOSTASIS

    Yves Laure Pimentel · 34問 · 2年前

    DISORDERS OF PRIMARY HEMOSTASIS

    DISORDERS OF PRIMARY HEMOSTASIS

    34問 • 2年前
    Yves Laure Pimentel

    PLATELET DISORDERS

    PLATELET DISORDERS

    Yves Laure Pimentel · 37問 · 2年前

    PLATELET DISORDERS

    PLATELET DISORDERS

    37問 • 2年前
    Yves Laure Pimentel

    CHARACTERISTICS OF CLOTTING FACTORS

    CHARACTERISTICS OF CLOTTING FACTORS

    Yves Laure Pimentel · 100問 · 2年前

    CHARACTERISTICS OF CLOTTING FACTORS

    CHARACTERISTICS OF CLOTTING FACTORS

    100問 • 2年前
    Yves Laure Pimentel

    4. CLASSIFICATION OF MACROPHAGE

    4. CLASSIFICATION OF MACROPHAGE

    Yves Laure Pimentel · 12問 · 2年前

    4. CLASSIFICATION OF MACROPHAGE

    4. CLASSIFICATION OF MACROPHAGE

    12問 • 2年前
    Yves Laure Pimentel

    3. NATURAL OR INNATE IMMUNITY

    3. NATURAL OR INNATE IMMUNITY

    Yves Laure Pimentel · 39問 · 2年前

    3. NATURAL OR INNATE IMMUNITY

    3. NATURAL OR INNATE IMMUNITY

    39問 • 2年前
    Yves Laure Pimentel

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    Yves Laure Pimentel · 55問 · 2年前

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    5. INTERNAL DEFENSE:SOLUBLE FACTORS (ACUTE PHASE REACTANTS)

    55問 • 2年前
    Yves Laure Pimentel

    6. PHAGOCYTOSIS Chemotaxis

    6. PHAGOCYTOSIS Chemotaxis

    Yves Laure Pimentel · 37問 · 2年前

    6. PHAGOCYTOSIS Chemotaxis

    6. PHAGOCYTOSIS Chemotaxis

    37問 • 2年前
    Yves Laure Pimentel

    8. NATURE OF ANTIGEN

    8. NATURE OF ANTIGEN

    Yves Laure Pimentel · 44問 · 2年前

    8. NATURE OF ANTIGEN

    8. NATURE OF ANTIGEN

    44問 • 2年前
    Yves Laure Pimentel

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    Yves Laure Pimentel · 50問 · 2年前

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    9. MAJOR HISTOCOMPATIBILITY COMPLEX/HUMAN LEUKOCYTE ANTIGEN

    50問 • 2年前
    Yves Laure Pimentel

    1. HISTORY

    1. HISTORY

    Yves Laure Pimentel · 69問 · 2年前

    1. HISTORY

    1. HISTORY

    69問 • 2年前
    Yves Laure Pimentel

    2. TYPES OF IMMUNITY

    2. TYPES OF IMMUNITY

    Yves Laure Pimentel · 38問 · 2年前

    2. TYPES OF IMMUNITY

    2. TYPES OF IMMUNITY

    38問 • 2年前
    Yves Laure Pimentel

    7. PHAGOCYTOSIS Engulfment and Digestion

    7. PHAGOCYTOSIS Engulfment and Digestion

    Yves Laure Pimentel · 21問 · 2年前

    7. PHAGOCYTOSIS Engulfment and Digestion

    7. PHAGOCYTOSIS Engulfment and Digestion

    21問 • 2年前
    Yves Laure Pimentel

    8. PHAGOCYTOSIS EXOCYTOSIS

    8. PHAGOCYTOSIS EXOCYTOSIS

    Yves Laure Pimentel · 15問 · 2年前

    8. PHAGOCYTOSIS EXOCYTOSIS

    8. PHAGOCYTOSIS EXOCYTOSIS

    15問 • 2年前
    Yves Laure Pimentel

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    Yves Laure Pimentel · 32問 · 2年前

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    10. DISEASE ASSOCIATED TO HUMAN LEUKOCYTE ANTIGEN (henry)

    32問 • 2年前
    Yves Laure Pimentel

    11. TRANSPLANTATION IMMUNOLOGY

    11. TRANSPLANTATION IMMUNOLOGY

    Yves Laure Pimentel · 30問 · 2年前

    11. TRANSPLANTATION IMMUNOLOGY

    11. TRANSPLANTATION IMMUNOLOGY

    30問 • 2年前
    Yves Laure Pimentel

    2. LYMPHOID ORGANS

    2. LYMPHOID ORGANS

    Yves Laure Pimentel · 38問 · 2年前

    2. LYMPHOID ORGANS

    2. LYMPHOID ORGANS

    38問 • 2年前
    Yves Laure Pimentel

    3. CLUSTER OF DIFFERENTIATION

    3. CLUSTER OF DIFFERENTIATION

    Yves Laure Pimentel · 48問 · 2年前

    3. CLUSTER OF DIFFERENTIATION

    3. CLUSTER OF DIFFERENTIATION

    48問 • 2年前
    Yves Laure Pimentel

    4. T-CELL DIFFERENTIATION

    4. T-CELL DIFFERENTIATION

    Yves Laure Pimentel · 35問 · 2年前

    4. T-CELL DIFFERENTIATION

    4. T-CELL DIFFERENTIATION

    35問 • 2年前
    Yves Laure Pimentel

    5. T CELL IMMUNODEFICIENCIES

    5. T CELL IMMUNODEFICIENCIES

    Yves Laure Pimentel · 18問 · 2年前

    5. T CELL IMMUNODEFICIENCIES

    5. T CELL IMMUNODEFICIENCIES

    18問 • 2年前
    Yves Laure Pimentel

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    Yves Laure Pimentel · 44問 · 2年前

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    6. STAGES IN B-CELL DIFFERENTIATION  PROPIMAP

    44問 • 2年前
    Yves Laure Pimentel

    7. B CELL IMMUNODEFICIENCIES

    7. B CELL IMMUNODEFICIENCIES

    Yves Laure Pimentel · 23問 · 2年前

    7. B CELL IMMUNODEFICIENCIES

    7. B CELL IMMUNODEFICIENCIES

    23問 • 2年前
    Yves Laure Pimentel

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    Yves Laure Pimentel · 34問 · 2年前

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    8. COMBINED T CELL AND B CELL DEFICIENCIES

    34問 • 2年前
    Yves Laure Pimentel

    9. COMPARISON OF T AND B CELLS

    9. COMPARISON OF T AND B CELLS

    Yves Laure Pimentel · 12問 · 2年前

    9. COMPARISON OF T AND B CELLS

    9. COMPARISON OF T AND B CELLS

    12問 • 2年前
    Yves Laure Pimentel

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    Yves Laure Pimentel · 16問 · 2年前

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    10. LABORATORY IDENTIFICATION OF LYMPHOCYTES

    16問 • 2年前
    Yves Laure Pimentel

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    Yves Laure Pimentel · 15問 · 2年前

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    11. NATURAL KILLER CELLS OR THIRD POPULATION CELL

    15問 • 2年前
    Yves Laure Pimentel

    12. ANTIBODY

    12. ANTIBODY

    Yves Laure Pimentel · 79問 · 2年前

    12. ANTIBODY

    12. ANTIBODY

    79問 • 2年前
    Yves Laure Pimentel

    13. TYPES OF ANTIBODIES

    13. TYPES OF ANTIBODIES

    Yves Laure Pimentel · 97問 · 2年前

    13. TYPES OF ANTIBODIES

    13. TYPES OF ANTIBODIES

    97問 • 2年前
    Yves Laure Pimentel

    14. MONOCLONAL ANTIBODIES

    14. MONOCLONAL ANTIBODIES

    Yves Laure Pimentel · 11問 · 2年前

    14. MONOCLONAL ANTIBODIES

    14. MONOCLONAL ANTIBODIES

    11問 • 2年前
    Yves Laure Pimentel

    1. INTERLEUKINS

    1. INTERLEUKINS

    Yves Laure Pimentel · 23問 · 2年前

    1. INTERLEUKINS

    1. INTERLEUKINS

    23問 • 2年前
    Yves Laure Pimentel

    2. INTERFERONS

    2. INTERFERONS

    Yves Laure Pimentel · 28問 · 2年前

    2. INTERFERONS

    2. INTERFERONS

    28問 • 2年前
    Yves Laure Pimentel

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    Yves Laure Pimentel · 8問 · 2年前

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    3. CYTOKINES IN THE INNATE AND ADAPTIVE IMMUNITY

    8問 • 2年前
    Yves Laure Pimentel

    4. COMPLEMENT SYSTEM

    4. COMPLEMENT SYSTEM

    Yves Laure Pimentel · 19問 · 2年前

    4. COMPLEMENT SYSTEM

    4. COMPLEMENT SYSTEM

    19問 • 2年前
    Yves Laure Pimentel

    15. COMPLEMENT SYSTEM

    15. COMPLEMENT SYSTEM

    Yves Laure Pimentel · 76問 · 2年前

    15. COMPLEMENT SYSTEM

    15. COMPLEMENT SYSTEM

    76問 • 2年前
    Yves Laure Pimentel

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    Yves Laure Pimentel · 21問 · 2年前

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    16. SYSTEM CONTROLS/COMPLEMENT REGULATION

    21問 • 2年前
    Yves Laure Pimentel

    17. COMPLEMENT AND DISEASE STATES

    17. COMPLEMENT AND DISEASE STATES

    Yves Laure Pimentel · 29問 · 2年前

    17. COMPLEMENT AND DISEASE STATES

    17. COMPLEMENT AND DISEASE STATES

    29問 • 2年前
    Yves Laure Pimentel

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    Yves Laure Pimentel · 19問 · 2年前

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    18. IMMUNOLOGIC ASSAYS OF INDIVIDUAL COMPONENTS (CLASSICAL)

    19問 • 2年前
    Yves Laure Pimentel

    19. CYTOKINES

    19. CYTOKINES

    Yves Laure Pimentel · 22問 · 2年前

    19. CYTOKINES

    19. CYTOKINES

    22問 • 2年前
    Yves Laure Pimentel

    20. INTERLEUKINS

    20. INTERLEUKINS

    Yves Laure Pimentel · 24問 · 2年前

    20. INTERLEUKINS

    20. INTERLEUKINS

    24問 • 2年前
    Yves Laure Pimentel

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    Yves Laure Pimentel · 21問 · 2年前

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    21. INTERFERONS, TNF, TGF, CHEMOKINE

    21問 • 2年前
    Yves Laure Pimentel

    1. SERO

    1. SERO

    Yves Laure Pimentel · 54問 · 2年前

    1. SERO

    1. SERO

    54問 • 2年前
    Yves Laure Pimentel

    2. PRECIPITATION

    2. PRECIPITATION

    Yves Laure Pimentel · 38問 · 2年前

    2. PRECIPITATION

    2. PRECIPITATION

    38問 • 2年前
    Yves Laure Pimentel

    3. PASSIVE IMMUNODIFFUSION

    3. PASSIVE IMMUNODIFFUSION

    Yves Laure Pimentel · 17問 · 2年前

    3. PASSIVE IMMUNODIFFUSION

    3. PASSIVE IMMUNODIFFUSION

    17問 • 2年前
    Yves Laure Pimentel

    4. OUCHTERLONY

    4. OUCHTERLONY

    Yves Laure Pimentel · 15問 · 2年前

    4. OUCHTERLONY

    4. OUCHTERLONY

    15問 • 2年前
    Yves Laure Pimentel

    5. ELECTROPHORETIC TECHNIQUE

    5. ELECTROPHORETIC TECHNIQUE

    Yves Laure Pimentel · 9問 · 2年前

    5. ELECTROPHORETIC TECHNIQUE

    5. ELECTROPHORETIC TECHNIQUE

    9問 • 2年前
    Yves Laure Pimentel

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    Yves Laure Pimentel · 11問 · 2年前

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    6. IMMUNOELECTROPHORESIS (DOUBLE DIFFUSION)

    11問 • 2年前
    Yves Laure Pimentel

    7. IMMUNOFIXATION ELECTROPHORESIS

    7. IMMUNOFIXATION ELECTROPHORESIS

    Yves Laure Pimentel · 29問 · 2年前

    7. IMMUNOFIXATION ELECTROPHORESIS

    7. IMMUNOFIXATION ELECTROPHORESIS

    29問 • 2年前
    Yves Laure Pimentel

    問題一覧

  • 1

    Which parameters are calculated rather than directly measured? A. Hematocrit and erythrocyte distribution width B. Erythrocyte count and leukocyte count C. Leukocyte count and hematocrit D. Platelet count and platelet volume

    A. Hematocrit and erythrocyte distribution width

  • 2

    If the RBC distribution on histogram demonstrates a homogenous pattern and small SD, the peripheral blood smear would probably exhibit: A. Extreme anisocytosis B. Very little anisocytosis C. A single population of spherocytes D. A single population of macrocytes

    B. Very little anisocytosis

  • 3

    The RDW and MCV are both quantitative descriptors of erythrocyte size. If both are increased, the most probable erythrocytic abnormality would be: A. Iron deficiency anemia B. Acquired aplastic anemia C. Megaloblastic anemia D. Hemoglobinopathy

    C. Megaloblastic anemia

  • 4

    In an erythrocyte histogram, the erythrocytes that are larger than normal will be to the ____ of the normal distribution curve. A. Right B. Left C. Middle D. Variable

    A. Right

  • 5

    RL flag except: A. Platelet clumps B. RBC fragments C. Giant platelets D. Cold agglutinins

    D. Cold agglutinins

  • 6

    Mean platelet volume (MPV): A. Analogous to MCHC B. Direct measure of platelet count C. Measurement of the average volume of platelets D. Comparison of the patient’s value to the normal value

    C. Measurement of the average volume of platelets

  • 7

    The MPV is often decreased in: A. Sickle cell anemia B. Megaloblastic anemia C. Idiopathic thrombocytopenic purpura D. After splenectomy

    B. Megaloblastic anemia

  • 8

    Normal PDW: A. Less than 5% B. Less than 10% C. Less than 15% D. Less than 20%

    D. Less than 20%

  • 9

    Which cell surface membrane marker is used for enumeration of HPC enumeration? HEMATOPOIETIC PROGENITOR CELLS A. CD 4 B. CD 8 C. CD 34 D. CD 45

    C. CD 34

  • 10

    The normal sequence of blood cell development is: A. Yolk sac—red bone marrow—liver and spleen B. Yolk sac—thymus—liver and spleen—red bone marrow C. Yolk sac—liver and spleen—red bone marrow D. Liver and spleen—yolk sac—red bone marrow

    C. Yolk sac—liver and spleen—red bone marrow

  • 11

    The abbreviation MAPCs stands for: A. Multiple adult progenitor cells B. Multipotent adult progenitor cells C. Many abnormal progenitor cells D. Multiply active potential cells

    B. Multipotent adult progenitor cells

  • 12

    The best source of active bone marrow from a 20- year-old would be: A. Iliac crest B. Femur C. Distal radius D. Tibia

    A. Iliac crest

  • 13

    Primary target cells of G-CSF, EXCEPT: A. Fibroblasts B. Leukemic myeloblasts C. Neutrophil precursors D. T and B cells

    D. T and B cells

  • 14

    Bone marrow cellularity refers to the ratio of: A. Red cell precursors to white cell precursors B. Hematopoietic tissue to adipose tissue C. Granulocytic cells to erythrocytic cells D. Extravascular tissue to intravascular tissue

    B. Hematopoietic tissue to adipose tissue

  • 15

    The maturational sequence(s) of the erythrocyte is (are): A. Rubriblast—prorubricyte—metarubricyte— rubricyte—reticulocyte—mature erythrocyte B. Rubriblast—prorubricyte—rubricyte— metarubricyte—reticulocyte—mature erythrocyte C. Pronormoblast—basophilic normoblast—polychromatophilic normoblast—orthochromic normoblast—reticulocyte—mature erythrocyte D. Both B and C

    D. Both B and C

  • 16

    The cell maturation sequence of the segmented neutrophil is: A. Promyelocyte—myeloblast—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN) B. Myeloblast—promyelocyte—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN) C. Monoblast—promyelocyte—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN) D. Promyelocyte—myelocyte—metamyelocyte— band or stab—segmented neutrophil (PMN)

    B. Myeloblast—promyelocyte—myelocyte— metamyelocyte—band or stab—segmented neutrophil (PMN)

  • 17

    The maturational sequence of the thrombocyte (platelet) is: A. Megakaryoblast—promegakaryocyte— megakaryocyte—metamegakaryocyte— thrombocyte B. Promegakaryocyte—megakaryocyte— metamegakaryocyte—thrombocyte C. Megakaryoblast—promegakaryocyte— megakaryocyte—thrombocyte D. Megakaryoblast—promegakaryocyte— metamegakaryocyte—thrombocyte

    C. Megakaryoblast—promegakaryocyte— megakaryocyte—thrombocyte

  • 18

    As a blood cell matures, the overall cell diameter in most cases: A. Increases B. Decreases C. Remains the same D. Variable

    B. Decreases

  • 19

    As a blood cell matures, the ratio of nucleus to cytoplasm (N:C) in most case: A. Increases B. Decreases C. Remains the same D. Variable

    B. Decreases

  • 20

    The chromatin pattern, in most cells, as the cell matures: A. Becomes more clumped B. Becomes less clumped C. Remains the same D. Variable

    A. Becomes more clumped

  • 21

    IN GENERAL, cytoplasmic color in younger cells: A. Pink B. Red C. Dark blue D. Light blue

    C. Dark blue

  • 22

    In the blast stage of DEVELOPMENT OF LEUKOCYTES, the cytoplasm of the cell is: A. Dark blue and lacks vacuoles B. Light blue and lacks granules C. Light blue and has specific granules D. Gray with many dark-blue granules

    B. Light blue and lacks granules

  • 23

    Hemoglobin appears for the first time in the ____ maturational stage of erythrocytes. A. Second B. Third C. Fourth D. Fifth

    B. Third

  • 24

    Which is the first stage of erythrocytic maturation in which the cytoplasm is pink due to the formation of hemoglobin? A. Reticulocyte B. Pronormoblast C. Basophilic normoblast D. Polychromatic normoblast

    D. Polychromatic normoblast

  • 25

    With a normal diet, an erythrocyte remains in the reticulocyte stage in the circulating blood for: A. 1 day B. 2.5 days C. 3 days D. 120 days

    A. 1 day

  • 26

    In a Wright-stained peripheral blood film, the reticulocyte will have a blue appearance. This is referred to as: A. Megaloblastic maturation B. Bluemia C. Polychromatophilia D. Erythroblastosis

    C. Polychromatophilia

  • 27

    The types of granulocytic leukocytes found in the proliferative compartment of the bone marrow are: A. Myeloblasts, myelocyte and metamyelocytes B. Myeloblasts, promyelocytes and metamyelocytes C. Myeloblasts, promyelocytes, myelocytes and metamyelocytes D. Myeloblasts, promyelocytes, myelocytes, metamyelocytes and band neutrophils

    C. Myeloblasts, promyelocytes, myelocytes and metamyelocytes

  • 28

    The types of granulocytic leukocytes found in the maturation-storage compartment of the bone marrow are: A. Metamyelocytes, band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils B. Only band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils C. Metamyelocytes, band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils D. Segmented neutrophils, immature and mature monocytes and mature lymphocytes

    A. Metamyelocytes, band form neutrophils, segmented neutrophils, mature eosinophils and mature basophils

  • 29

    Identify the cell with these characteristics: prominent primary granules that are rich in myeloperoxidase and chloroacetate esterase and have a diameter of 14 to 20 µm. A. Myeloblast B. Promyelocyte C. Myelocyte D. Promonocyte

    B. Promyelocyte

  • 30

    The earliest granulocytic maturational stage in which secondary or specific granules appear is: A. Myeloblast B. Monoblast C. Promyelocyte D. Myelocyte

    D. Myelocyte

  • 31

    The most mature granulocyte precursor that can undergo mitosis is the: A. Myeloblast B. Promyelocyte C. Myelocyte D. Metamyelocyte

    C. Myelocyte

  • 32

    Which of the following can differentiate metamyelocytes from other stages of granulocyte maturation? A. Presence of specific granules B. Indentation of nucleus C. Absence of nucleoli D. Color of cytoplasm

    B. Indentation of nucleus

  • 33

    The stage in neutrophilic development in which the nucleus is indented in a kidney bean shape and the cytoplasm has secondary granules that are lavender in color is the: A. Band B. Myelocyte C. Promyelocyte D. Metamyelocyte

    D. Metamyelocyte

  • 34

    Which of the following are contents of basophilic granules? A. Heparin B. Histamine C. Myeloperoxidase D. Both A and B

    D. Both A and B

  • 35

    The half-life of circulating granulocytes in the blood is estimated to be: A. 2.5 to 5 hours B. 7 to 10 hours C. 24 hours D. 2 days

    B. 7 to 10 hours

  • 36

    A characteristic of a segmented neutrophil is: A. Large orange granules B. An elongated and curved nucleus C. Light sky-blue cytoplasm D. Greatest number of WBCs in the peripheral blood of an adult

    D. Greatest number of WBCs in the peripheral blood of an adult

  • 37

    A characteristic of mature eosinophil is: A. Large orange granules B. Elongated and curved nucleus C. Light, sky-blue cytoplasm D. Kidney bean-shaped nucleus

    A. Large orange granules

  • 38

    A characteristic of mature monocyte: A. Large orange granules B. Elongated and curved nucleus C. Light, sky-blue cytoplasm D. Kidney bean-shaped nucleus

    D. Kidney bean-shaped nucleus

  • 39

    A characteristic of mature lymphocyte is: A. Large, orange granules B. Elongated and curved cytoplasm C. Light, sky-blue cytoplasm D. Kidney bean-shaped nucleus

    C. Light, sky-blue cytoplasm

  • 40

    An increase in metamyelocytes, myelocytes and promyelocytes can be referred to as: A. Leukocytopenia B. Shift to the right C. Shift to the left D. Pelger-Huet anomaly

    C. Shift to the left

  • 41

    The major function of the neutrophilic granulocytes: A. Antibody production B. Destruction of parasites C. Phagocytosis D. Suppression of inflammation

    C. Phagocytosis

  • 42

    The principal leukocyte type involved in phagocytosis: A. Monocyte B. Neutrophil C. Eosinophil D. Basophil

    B. Neutrophil

  • 43

    The major function of eosinophil is: A. Suppression of inflammatory reactions B. Destruction of protozoa C. Participation in anaphylaxis D. Phagocytosis

    A. Suppression of inflammatory reactions

  • 44

    Which of the following is/are characteristic/s of erythropoietin? A. Glycoprotein B. Secreted by the liver C. Secreted by the kidneys D. All of the above

    D. All of the above

  • 45

    Stimulation of erythropoietin is caused by: A. Tissue hypoxia B. Hypervolemia C. Inflammation D. Infection

    A. Tissue hypoxia

  • 46

    Biochemical abnormalities characteristic of polycythemia vera include: A. Increased serum B12 binding capacity B. Hypohistaminemia C. Hypouricemia D. Decreased leukocyte alkaline phosphatase activity

    A. Increased serum B12 binding capacity

  • 47

    Increased erythropoietin production in secondary polycythemia can be caused by: A. Chronic lung disease B. Smoking C. Renal neoplasms D. All of the above

    D. All of the above

  • 48

    Relative polycythemia exists when: A. Increased erythropoietin is produced B. Total blood volume is expanded C. Plasma volume is increased D. Plasma volume is decreased

    D. Plasma volume is decreased

  • 49

    The primary pathophysiologic mechanism of anemia associated with chronic kidney disease is: A. Inadequate production of erythropoietin B. Excessive hemolysis C. Hematopoietic stem cell mutation D. Toxic destruction of stem cells

    A. Inadequate production of erythropoietin

  • 50

    D. Toxic destruction of stem cells 650. Effect of increased amounts of 2,3-DPG to oxygen affinity of the hemoglobin molecule. A. Increases B. Decreases C. Do not alter D. Variable

    B. Decreases

  • 51

    The most common erythrocytic enzyme deficiency involving the Embden-Meyerhof glycolytic pathway is a deficiency of: A. ATPase B. Pyruvate kinase C. Glucose-6-phosphate dehydrogenase D. Lactic dehydrogenase

    B. Pyruvate kinase

  • 52

    The final steps in heme synthesis, including the formation of protoporphyrin take place in: A. Cell’s nucleus B. Cell’s cytoplasm C. Spleen D. Mitochondria

    D. Mitochondria

  • 53

    In an alkaline pH (pH of 8.6) electrophoresis is performed, hemoglobin E has the same mobility as hemoglobin: A. S B. F C. A D. C

    D. C

  • 54

    The type of hemoglobin that is detectable with the Kleihauer-Betke test is: A. A B. A2 C. F D. S

    C. F

  • 55

    f female patient is diagnosed with anemia and her follow-up assays indicated blood serum results of increased bilirubin and decreased haptoglobin and hemosiderin in her urinary sediment, what is the most probable diagnosis? A. Extravascular catabolism B. Intravascular catabolism C. Defective hemoglobin synthesis D. Thalassemia

    B. Intravascular catabolism

  • 56

    If you are grading changes in erythrocytic size or shape using a scale of 0 to 4+ and MANY erythrocytes deviate from normal per microscopic field, the typical score would be A. 1+ B. 2+ C. 3+ D. 4+

    C. 3+

  • 57

    Which of the following is associated with a defect in nuclear maturation? A. Microcytes B. Sickle cells C. Megalocytes D. Acanthocytes

    C. Megalocytes

  • 58

    Which of the following represents an imbalance between erythrocytic and plasma lipids? A. Microcytes B. Sickle cells C. Macrocytes D. Acanthocytes

    D. Acanthocytes

  • 59

    Acanthocytes may be associated with the clinical condition of: A. Iron deficiency anemia B. Abetalipoproteinemia C. Pernicious anemia D. No related disease state

    B. Abetalipoproteinemia

  • 60

    Spherocytes: A. Short, scalloped, or spike-like projections that are regularly distributed around the cell B. Fragments of erythrocytes C. The scooped-out part of an erythrocyte that remains after a blister cell ruptures D. Compact round shape

    D. Compact round shape

  • 61

    Dacryocytes may be seen in: A. Hepatic disorders B. Hemolytic disease of the fetus and newborn C. Hemoglobinopathies D. Pernicious anemia

    D. Pernicious anemia

  • 62

    Basophilic stippling represents: A. DNA B. Precipitated denatured hemoglobin C. Granules of ribosomes and RNA D. Aggregates of iron, mitochondria and ribosomes

    C. Granules of ribosomes and RNA

  • 63

    Pappenheimer bodies represent: A. DNA B. Precipitated denatured hemoglobin C. Granules of ribosomes and RNA D. Aggregates of iron, mitochondria and ribosomes

    D. Aggregates of iron, mitochondria and ribosomes

  • 64

    Fanconi’s anemia is associated with abnormal genes located on chromosomes: A. 9, 20 B. 5, 22 C. 9, 12 D. 8, 23

    A. 9, 20

  • 65

    The average adult has ____g of total iron. A. 0.2 to 1.4 B. 1.5 to 3.4 C. 3.5 to 5.0 D. 5.1 to 10.0

    C. 3.5 to 5.0

  • 66

    The cytochemical stain that can demonstrate iron, hemosiderin and ferritin is: A. New methylene blue B. Romanowsky C. Prussian blue D. Wright-Giemsa

    C. Prussian blue

  • 67

    I What is the major metabolically available storage form of iron in the body? A. Hemosiderin B. Ferritin C. Transferrin D. Hemoglobin

    B. Ferritin

  • 68

    The total iron-binding capacity (TIBC) of the serum is an indirect measure of which iron-related protein? A. Hemosiderin B. Ferritin C. Transferrin D. Hemoglobin

    C. Transferrin

  • 69

    The transfer of iron from the enterocyte into the plasma is REGULATED by: A. Transferrin B. Ferroportin C. Hephaestin D. Hepcidin

    D. Hepcidin

  • 70

    In stage 3 IDA, the erythrocyte indices are typically: A. MCV increased, MCH decreased, and MCHC decreased B. MCV decreased, MCH decreased, and MCHC decreased C. MCV decreased, MCH increased, and MCHC decreased D. MCV decreased, MCH decreased, and MCHC normal

    B. MCV decreased, MCH decreased, and MCHC decreased

  • 71

    In megaloblastic anemia, the typical erythrocytic indices are: A. MCV increased, MCH increased, and MCHC normal B. MCV increased, MCH variable, and MCHC normal C. MCV increased, MCH decreased, and MCHC normal D. MCV normal, MCH increased, and MCHC norma

    A. MCV increased, MCH increased, and MCHC normal

  • 72

    Which of the following can be found in a patient with classic megaloblastic anemia? A. Ovalocytes and hypersegmented neutrophils B. Hypochromic macrocytes and variant lymphocytes C. Howell-Jolly bodies and Pappenheimer bodies D. Lymphocytosis

    A. Ovalocytes and hypersegmented neutrophils

  • 73

    n cold-type AIHA: A. IgM, usually anti-I is present B. Rh antibodies are the most frequent cause C. IgM usually occurs in newborn infants D. Autoantibodies are present

    A. IgM, usually anti-I is present

  • 74

    Which of the following is NOT associated with hemolytic anemia? A. Decrease hemoglobin and packed cell volume B. Increased reticulocyte count C. Increased serum haptoglobin D. Decreased erythrocyte survival

    C. Increased serum haptoglobin

  • 75

    Paroxysmal nocturnal hemoglobinuria exhibits sensitivity of one population of red cells to: A. Warm antibodies B. Cold antibodies C. Complement D. Either A and B

    C. Complement

  • 76

    The defect in PNH is a/an ____ associated defect of the RBC membrane. A. Structural protein B. Hemoglobin C. Antibody D. Enzyme

    A. Structural protein

  • 77

    What factors contribute to the sickling of erythrocytes in sickle cell disease crisis? A. Increase in blood pH and increase in oxygen B. Extremely hot weather C. Extremely reduced oxygen and increased acidity in the blood D. Sickling is spontaneous

    C. Extremely reduced oxygen and increased acidity in the blood

  • 78

    Lymphocyte development in the thymus and bursal equivalent are: A. Antigen-independent B. Antigen-dependent C. Antibody-independent D. Antibody-dependent

    A. Antigen-independent

  • 79

    Which of the following is characteristic of Dohle body inclusions? A. Gigantic peroxidase positive deposits B. Precipitated mucopolysaccharides C. Dark blue cytoplasmic inclusions D. Single or multiple pale-blue staining inclusions

    D. Single or multiple pale-blue staining inclusions

  • 80

    Which of the following is characteristic of MayHegglin anomaly? A. Gigantic peroxidase-positive deposits B. Precipitated mucopolysaccharides C. Dohle body-like inclusions and giant platelets D. Single or multiple pale blue staining inclusions

    C. Dohle body-like inclusions and giant platelets

  • 81

    Cytoplasmic inclusion in Alder-Reilly anomaly can resemble: A. Dohle bodies B. Toxic granulation C. Auer rods D. Parasites

    B. Toxic granulation

  • 82

    azy leukocyte syndrome is associated with the: A. Neutrophilic series B. Monocytic-macrophage series C. Lymphocytic series D. Erythrocytic series

    A. Neutrophilic series

  • 83

    Smudge cells are associated with: A. Niemann Pick disease and Burkitt’s lymphoma B. CLL C. Leukosarcoma D. Natural artifact

    B. CLL

  • 84

    The EBV infects: A. T cells B. B cells C. Monocytes D. Macrophages

    B. B cells

  • 85

    Multiple myeloma is a disorder of: A. T lymphocytes B. Megakaryocytes C. Plasma cells D. Lymph notes

    C. Plasma cells

  • 86

    WM is characterized by increased levels of: A. IgG B. IgM C. IgD D. IgA

    B. IgM

  • 87

    According to the WHO classification, except in leukemias with specific genetic anomalies, the minimal percentage of blasts necessary for a diagnosis of acute leukemia is: A. 10% B. 20% C. 30% D. 50%

    B. 20%

  • 88

    Acute leukemia can be described as being: A. Short duration with many mature leukocyte forms in the peripheral blood B. Short duration with many immature leukocyte forms in the peripheral blood C. Short duration with little alteration of the leukocytes of the peripheral blood D. Long duration with many mature leukocyte forms in the peripheral blood

    B. Short duration with many immature leukocyte forms in the peripheral blood

  • 89

    Myeloid without maturation acute leukemias is classified as: A. M1 B. M4 C. M5 D. L1

    A. M1

  • 90

    Myeloblasts, promyelocytes and myelocytes predominate in: A. M2 B. M3 C. M4 D. M6

    A. M2

  • 91

    Many coarsely granular promyelocytes with dumbbell-shaped or bilobed nuclei predominate in: A. M2 B. M3 C. M4 D. M6

    B. M3

  • 92

    Myeloid and monocytic acute leukemias are classified as FAB: A. M1 B. M4 C. M5 D. L1

    B. M4

  • 93

    Monocytic acute leukemia is classified as FAB: A. M1 B. M4 C. M5 D. L1

    C. M5

  • 94

    Immature leukocytic and erythrocytic cell types predominate in: A. M2 B. M3 C. M4 D. M6

    D. M6

  • 95

    Chloromas are associated with: A. FAB M1 B. FAB M3 C. FAB M4 D. FAB M5

    A. FAB M1

  • 96

    Myeloperoxidase (MPO) and Sudan Black B (SBB) staining results: A. Opposite B. Parallel C. Undetermined D. Variable

    B. Parallel

  • 97

    Which cell type demonstrates the most intense peroxidase reaction? A. Neutrophil B. Basophil C. Lymphocyte D. Monocyte

    A. Neutrophil

  • 98

    Cells do not exhibit myeloperoxidase (MPO) activity: A. Eosinophils B. Neutrophils C. Lymphocytes D. Monocytes

    C. Lymphocytes

  • 99

    Detects lymphocytic cells and certain abnormal ERYTHROCYTIC CELLS by staining of cytoplasmic GLYCOGEN: A. MPO B. SBB C. PAS D. Tdt

    C. PAS

  • 100

    A laboratory assay that can be used to differentiate a leukemoid reaction from chronic myelogenous leukemia is: A. Leukocyte alkaline phosphatase (LAP) stain B. Erythrocyte sedimentation rate (ESR) C. Assessment of the shift to the left D. Absolute neutrophil count

    A. Leukocyte alkaline phosphatase (LAP) stain