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HEMATOLOGY
  • Yves Laure Pimentel

  • 問題数 100 • 7/26/2024

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    問題一覧

  • 1

    The abnormal protein frequently found in the urine of persons with multiple myeloma is: a. Albumin b. Globulin c. IgG d. Bence Jones

    d. Bence Jones

  • 2

    The description of poikilocytosis is: a. Variation in erythrocyte size b. Larger than normal c. Smaller than normal d. Variation in erythrocyte shape

    d. Variation in erythrocyte shape

  • 3

    The alkaline denaturation test detects the presence of hemoglobin: a. A1c b. F c. C d. S

    b. F

  • 4

    The reagent used in the traditional sickle screening test is: a. Sodium chloride b. Sodium metabisulfite d. Sodium citrate d. None of the above

    b. Sodium metabisulfite

  • 5

    What is the immature erythrocyte found in the bone marrow with following characteristics: 12 to 17 mm in diameter, N:C ratio of 4:1, nucleoli not usually apparent, and basophilic cytoplasm? a. Rubriblast b. Reticulocyte c. Metarubricyte d. Prorubricyte

    d. Prorubricyte

  • 6

    Which antibody test has replaced the LE cell preparation in the diagnosis of SLE? a. Rheumatoid arthritis factor b. ANA test c. Complement fixation test d. Antibody Smith test

    b. ANA test

  • 7

    Which of the following poikilocyte is being illustrated? a. Codocytes b. Elliptocytes c. Blister cells d. Stomatocytes

    a. Codocytes

  • 8

    Which clotting factors (cofactors) are inhibited by protein S? a. Factor V and X b. Factor Va and VIIIa c. Factor VIII and IX d. Factor VIII and X

    b. Factor Va and VIIIa

  • 9

    IDENTIFY

    Elliptocyte HEREDITARY ELLIPTOCYTOSIS GERBICH NULL/ LEACH PHENOTYPE

  • 10

    The deficient factor is factor VIII. What would be the result for PT, PTT, and TCT, respectively, using clot-based screening assays? a. Normal, prolonged, normal b. Prolonged, prolonged, prolonged c. Prolonged, normal, normal d. Prolonged, normal, prolonged

    a. Normal, prolonged, normal

  • 11

    IDENTIFY

    Howell-Jolly bodies

  • 12

    Hematopoietic stem cells produce all lineages of blood cells in sufficient quantities over the lifetime of an individual because they: a. Are unipotent b. Have the ability of self-renewal by asymmetric division c. Are present in large numbers in the bine marrow niches d. Have a low mitotic potential in response to growth factors.

    b. Have the ability of self-renewal by asymmetric division

  • 13

    IDENTIFY

    Basophilic stippling

  • 14

    Agents that are capable of aggregating platelets include: a. Collagen b. Thrombin c. Serotonin d. All of the above

    d. All of the above

  • 15

    The function of thromboplastin in the prothrombin test is to provide _____ to the assay. a. Kaolin b. Fibrinogen c. Phospholipoprotein d. Thrombin

    c. Phospholipoprotein

  • 16

    Refer to the following results: PT= prolonged APTT= prolonged PLT count= decreased Which disorder may be indicated? a. Factor VIII deficiency b. von Willebrand disease c. Disseminated intravascular coagulation d. Factor IX deficiency

    c. Disseminated intravascular coagulation

  • 17

    When a specimen has been flagged as being icteric by an automated coagulation analyzer, which method would be most susceptible to erroneous results because of interfering substance? a. Mechanical clot detection b. Immunologic antigen-antibody reaction detection c. Photo-optical clot detection d. Chromogenic end-point detection

    c. Photo-optical clot detection

  • 18

    What influence does the Philadelphia (Ph1) chromosome have on the prognosis of patients with CML? a. It is not predictive b The prognosis is better if Ph1 is present c. The prognosis is worse if Ph1 is present d. The disease usually transforms into AML when Ph1 is present

    b The prognosis is better if Ph1 is present

  • 19

    If a blood smear stains too red on microscopic examination of Wright-stained preparation, possible causes include that: a. The staining time was too long b. The stain was too basic c. The buffer was too acidic and the exposure time was too short d. The buffer was too basic and the exposure time was too long

    c. The buffer was too acidic and the exposure time was too short

  • 20

    Platelet aggregation will occur with the end product of: a. Cyclooxygenase b. Arachidonic acid c. Prostacyclin d. Thromboxane A2

    d. Thromboxane A2

  • 21

    The clot retraction test is: a. A visible reaction to the activation of platelet actomyosin (thrombasthenin) b. A reflection of the quantity and quality of platelets and other factors c. A measurement of the ability of platelets to stick to glass d. A measurement of the cloudiness of blood

    b. A reflection of the quantity and quality of platelets and other factors

  • 22

    Patient with thrombocytopenia, decrease in hemoglobin, fragmented RBCs. Which of the following diseases is the most probable cause? a. HUS b. ITP c. HHT d. None of the above

    a. HUS

  • 23

    Acanthocytes (Spur cells) may be associated with the clinical condition of: a. Iron deficiency anemia b. Abetalipoproteinemia c. Pernicious anemia d. None of the above

    b. Abetalipoproteinemia

  • 24

    IDENTIFY

    Hb SC crystals

  • 25

    Which characteristic is inaccurate with respect to the anticoagulant K3 EDTA? a. Removes ionized calcium from fresh whole blood by the process of chelation b. Is the most commonly used anticoagulant in hematology c. Is conventionally placed in lavender-stoppered tubes. d. Is used for most routine coagulation studies

    d. Is used for most routine coagulation studies

  • 26

    The stages of neutrophilic granulocyte development are a. promyelocyte, myeloblast, myelocyte, metamyelocyte, and band and segmented neutrophils b. myeloblast, promyelocyte, myelocyte, metamyelocyte, and band and segmented neutrophils c. myelocyte, myeloblast, promyelocyte, metamyelocyte, and band and segmented neutrophils d. myeloblast, promyelocyte, metamyelocyte, myelocyte, and band and segmented neutrophils

    b. myeloblast, promyelocyte, myelocyte, metamyelocyte, and band and segmented neutrophils

  • 27

    IDENTIFY

    Schistocytes MICROANGIPATHIC HEMOLYTIC ANEMIA -- HUS -- TTP -- DIC -- HELLP SYNDROME MACROANGIPATHIC HEMOLYTIC ANEMIA -- WARING BLENDER SYNDROME (HEART VALVES) -- MARCH HEMOGLOBINURIA

  • 28

    If a child ingested rat poison, which of the following tests should be performed to test the effect of the poison on the child’s coagulation mechanism? a. aPTT b. PT c. Fibrinogen assay d. None of the above

    b. PT

  • 29

    What clinical condition will produce a decreased Westergren ESR value? a. Polycythemia vera b. Acute leukemia c. Viral infection d. Megaloblastic anemia

    a. Polycythemia vera

  • 30

    Which test is most affected when there is excessive anticoagulant? a. RBC count b. ESR c. Hemoglobin d. Hematocrit

    d. Hematocrit

  • 31

    IDENTIFY

    Spherocytes MCHC >36% IMMUNE HEMOLYTIC ANEMIA -- HDFN -- BURNS -- HEREDITARY SPHEROCYTOSIS

  • 32

    What growth factors is produced by the kidneys and is used to treat anemia associated with kidney disease? a. EPO b. TPO c. KIT ligand d. G-CSF

    a. EPO

  • 33

    Cells that produces antibodies and lymphokines: a. Erythrocytes b. Granulocytes c. Lymphocytes d. Thrombocytes

    c. Lymphocytes

  • 34

    What is the formula for RDW? a. SD x 100/mean b. HCT/RBC x 10 c. HGB/RBC x 10 d. HGB/HCT x 100

    a. SD x 100/mean

  • 35

    The intrinsic pathway of coagulation BEGINS with the activation of _____ in the early stage. a. Factor II b. Factor I c. Factor XII d. Factor V

    c. Factor XII

  • 36

    Contains DNA or nuclear fragments: a. Basophilic stippling b. Howell-Jolly body c. Heinz body d. Pappenheimer bodies

    b. Howell-Jolly body

  • 37

    Which of the following metabolic pathway prevents oxidation of heme iron? a. Embden-Meyerhof pathway b. Hexose-monophosphate pathway c. Methemoglobin reductase pathway d. Luebering-Rapaport pathway

    c. Methemoglobin reductase pathway

  • 38

    Microspherocytes may be seen in: a. HD (Hepatic disease) b. HDFN (Hemolytic disease of the fetus and newborn) c. PA (Pernicious anemia) d. HB (Hemoglobinopathies)

    b. HDFN (Hemolytic disease of the fetus and newborn)

  • 39

    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

  • 40

    The abbreviation laser stands for a. light-associated simulated emission of radiation b. largely amplified by simulated emission of radiation c. light amplified by stimulated emission of radiation d. liquid amplified by stimulated emission of radiation

    c. light amplified by stimulated emission of radiation

  • 41

    f you are grading changes in erythrocytic size or shape using a scale of 0 to 4+ and many erythrocyte deviate from normal per microscopic field, the typical score would be: a. 1+ b. 2+ c. 3+ d. 4+

    c. 3+

  • 42

    Using white blood cell as the reference, what is the effect of leukocytosis in the ESR? a. Increased b. Decreased c. Variable d. None of the above

    b. Decreased

  • 43

    Which of the cytokine has the current/potential therapeutic application as an adjuvant for infectious disease therapy? a. IL-3 b. GM-CSF c. IL-12 d. IFN-a

    c. IL-12

  • 44

    If globin synthesis is insufficient in a person, iron accumulates in the cell as _______ aggregates a. Transferrin b. Ferritin c. Albumin d. Heme

    b. Ferritin

  • 45

    Electrical impedance principle of cell counting was originally developed by: a. Coulter b. Abbott c. Beckman d. Sysmex

    a. Coulter

  • 46

    IDENTIFY

    Sickle cells DREPANOCYTES

  • 47

    Using white blood cell as the reference, what is the effect of leukemia in the ESR? a. Increased b. Decreased c. Variable d. None of the above

    a. Increased

  • 48

    IDENTIFY

    ACANTHOCYTES ABETALIPOPROTEINEMIA MCLEOD PHENOMENON

  • 49

    A combined scatter histogram measure: a. Overall size versus nuclear size b. Cell size and granularity c. Cell shape and cytoplasmic color d. Cytoplasm to nucleus ratio

    b. Cell size and granularity

  • 50

    The greatest portion of operational body iron is normally contained in what compound? a. Hemoglobin b. ferritin c. Cytochromes d. Myoglobin

    a. Hemoglobin

  • 51

    In Gaucher disease, as the result of βglucocerebrosidase deficiency, what accumulates in (macrophages) histiocytes? a. Glucocerebroside and sphingomyelin b. Glucocerebroside c. Sphingomyelin d. None of the above

    b. Glucocerebroside

  • 52

    Fletcher factor: a. Prekallikrein b. HMWK c. Factor XI d. Factor XII

    a. Prekallikrein

  • 53

    Promyelocytes predominate in the bone marrow: a. M1 b. M2 c. M3 d. M4

    c. M3

  • 54

    The average diameter of a normal erythrocyte is ____ micrometer. a. 5.2 µm b. 6.4 µm c. 7.2 µm d. 8.4 µm

    c. 7.2 µm

  • 55

    Occur when there is a breakage in two chromosomes and each of the broken pieces reunites with another chromosomes: a. Inversion b. Translocation c. Mutation d. None of the above

    b. Translocation

  • 56

    Acceptable limits of control value must fall: a. Within ±1SD of the mean b. Within 1 and 2 SD of the mean c. Within ±2 SD of the mean d. Within ±3 SD of the mean

    c. Within ±2 SD of the mean

  • 57

    What is the most common mechanism resulting in hereditary stomatocytosis? a. A deficient cytoskeletal protein b. Inability to repair oxidative stress damage c. Abnormal Na+/K+ permeability d. ATP depletion due to glycolytic enzyme deficiency

    c. Abnormal Na+/K+ permeability

  • 58

    Which of the following blood film findings indicates EDTA-induced pseudo thrombocytopenia? a. The platelets are pushed to the feathered end b. The platelets are adhering to WBCs c. No platelets at all are seen on the film d. The slide has a bluish discoloration when examined macroscopically

    b. The platelets are adhering to WBCs

  • 59

    Niemann-Pick disease affects which cell type? a. Neutrophils b. Lymphocytes c. Erythrocytes d. Platelets

    b. Lymphocytes

  • 60

    IDENTIFY

    Hb C crystals HEMOGLOBIN C DISEASE

  • 61

    IDENTIFY

    Ovalocyte LARGE OVALOCYTES -- MEGALOBLASTIC ANEMIA

  • 62

    . Increased amounts of 2,3-BPG ____ the oxygen affinity of the hemoglobin molecule. a. Increases b. Decreases c. Does not alter d. None of the above

    b. Decreases

  • 63

    IDENTIFY GIVEN DSE (2)

    Echinocyte (Burr cell) UREMIA PK DEFICIENCY

  • 64

    Physiologic programmed cell death: a. Angiogenesis b. Apoptosis c. Necrosis d. Apohematics

    b. Apoptosis

  • 65

    Which of the following refers to the number, form, size, and arrangement of chromosomes within the nucleus? a. Punnett squares b. Karyotyping c. Phage typing d. None of the above

    b. Karyotyping

  • 66

    In the photo-optical method, the change in light transmission versus the _____ is used to determine the activity of coagulation factors or stages. a. amount of patient’s plasma b. amount of test reagent c. time d. temperature

    c. time

  • 67

    Which of the following poikilocyte is present? a. Codocytes b. Elliptocytes c. Blister cells d. Stomatocytes

    d. Stomatocytes

  • 68

    Disease characterized with a poikilocyte with membrane folded over (Fold cells): a. Sickle cell anemia b. Hemoglobin C disease c. Hemoglobin H disease d. Bart’s hemoglobin

    b. Hemoglobin C disease

  • 69

    The normal range for reticulocytes in adults is: a. 0 to 0.5% b. 0.5% to 1.0% c. 0.5% to 1.5% d. 1.5% to 2.5%

    c. 0.5% to 1.5%

  • 70

    Anticoagulant to avoid platelet satellitism: a. EDTA b. Oxalate c. Citrate d. Heparin

    c. Citrate

  • 71

    The major application of flow-cytometry is: a. Determining cell size and granularity b. Sorting of cells and cellular identification using monoclonal antibodies c. Treating cancer cells and identifying specific virus types d. Counting leukocytes and platelets

    b. Sorting of cells and cellular identification using monoclonal antibodies

  • 72

    IDENTIFY

    Teardrop cells DACRYOCYTES -- MMM/ PRIMARY MYELOFIBROSIS (MYELOID METAPLASIA WITH MYELOFIBROSIS -- MYELOPTHISIC

  • 73

    The bleeding time test measures a. the ability of platelets to stick together b. platelet adhesion and aggregation on locally injured vascular subendothelium c. the quantity and quality of platelets d. antibodies against platelets

    b. platelet adhesion and aggregation on locally injured vascular subendothelium

  • 74

    PT is performed in what temperature? a. 4 degrees Celsius b. 20 degrees Celsius c. 37 degrees Celsius d. 38 degrees Celsius

    c. 37 degrees Celsius

  • 75

    . Fibrinogen level in patients with hemophilia A, B and C? a. Decreased, normal, decreased b. Normal, normal, normal c. Decreased, decreased, decreased d. Normal, decreased, decreased

    b. Normal, normal, normal

  • 76

    Paroxysmal nocturnal hemoglobinuria exhibits sensitivity of one population of red blood cells to: a. Warm antibodies b. Cold antibodies c. Complement d. Either A or B

    c. Complement

  • 77

    As the red blood cell matures, the overall cell diameter: a. Increases b. Decreases c. Remains the same d. None of the above

    b. Decreases

  • 78

    Abnormal results in dysfibrinogenemia, except: a. PT b. aPTT c. TT d. Fibrinogen level

    d. Fibrinogen level

  • 79

    What is the appropriate procedure and characteristic for the Westergren method? a. The diluting solution lyses erythrocytes with propylene glycol and contains sodium carbonate and water. b. The procedure measures the rate of erythrocyte settling. c. Ferrous ions are oxidized to the ferric state. d. The diluting solution is either 1% HCl or 2% acetic acid.

    b. The procedure measures the rate of erythrocyte settling.

  • 80

    Bite cells: a. PK deficiency b. G6PD deficiency c. PK and G6PD deficiency d. None of the above

    b. G6PD deficiency

  • 81

    A screening test for PNH is: a. Heat instability test b. Sucrose hemolysis test c. Osmotic fragility d. Dithionite solubility

    b. Sucrose hemolysis test

  • 82

    Azurophilic granules were produced in what stage? a. Promyelocyte b. Myelocyte c. Metamyelocyte d. Band

    a. Promyelocyte

  • 83

    Megakaryopoiesis is associated with: a. Endomitosis b. Meiosis c. Mitosis d. None of the above

    a. Endomitosis

  • 84

    In the preparation of films for reticulocyte counting, what is the ratio of blood to the stain? a. 1:2 b. 2:1 c. 3:1 d. 1:1

    d. 1:1

  • 85

    Which of the following condition is characterized by the absence of CD55 (DAF) and CD59 (MIRL) on the surface of the RBCs rendering the it susceptible to spontaneous lysis by complement? a. PCH b. PNH c. HUS d. DIC

    b. PNH

  • 86

    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. In the middle d. Bimodal

    a. Right

  • 87

    An example of an acquired platelet dysfunction: a. Uremia b. von Willebrand’s disease c. Aspirin ingestion d. None of the above

    a. Uremia

  • 88

    An acute leukemia can be described as being: a. of short duration with many mature leukocyte forms in the peripheral blood b. of short duration with many immature leukocyte forms in the peripheral blood c. of short duration with little alteration of the leukocytes of the peripheral blood d. of long duration with many mature leukocyte forms in the peripheral blood

    b. of short duration with many immature leukocyte forms in the peripheral blood

  • 89

    The cellular ultrastructural component unique to platelet is: a. Cytoplasmic membrane b. Mitochondria c. Microtubules d. Glycocalyx

    d. Glycocalyx

  • 90

    Schistocytes: a. Fragmented RBC b. RBC with no central pallor c. Crenated RBC d. Swollen RBC

    a. Fragmented RBC

  • 91

    The delta check method of quality control a. uses the patient’s own data to monitor population values b. uses batches of 20 samples to track MCV, MCH, and MCHC values c. compares the patient’s leukocyte and platelet counts with his or her previous results d. monitors the patient’s values within two SDs of the mean

    c. compares the patient’s leukocyte and platelet counts with his or her previous results

  • 92

    Three-part differential: a. Lymphocytes, monocytes, and granulocytes b. Lymphocytes, mononuclear, and granulocytes c. Lymphocytes, monocytes, neutrophil d. Lymphocyte, monocyte, neutrophil, eosinophil

    b. Lymphocytes, mononuclear, and granulocytes

  • 93

    If the RBC distribution on a histogram demonstrates a homogenous pattern and a 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

  • 94

    Single factor deficiency with normal PT, PTT, and TCT: a. I b. XI c. XIII d. II

    c. XIII

  • 95

    The RDW and MCV are both quantitative descriptors of RBC 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

  • 96

    The WHO classification requires what percentage for the blast count in the blood or bone marrow for the diagnosis of AML? a. At least 30% b. At least 20% c. At least 10% d. Any percentage

    b. At least 20%

  • 97

    What is the appropriate reagent for reticulocyte counting? a. New methylene blue b. Phloxine B c. Solution that can lyse erythrocyte and darken the cell to be counted d. None of the above

    a. New methylene blue

  • 98

    Which one of the following cells is a product of the CLP? a. Megakaryocytes b. T lymphocyte c. Erythrocyte d. Granulocyte

    b. T lymphocyte

  • 99

    Which organ is the site of sequestration of platelets? a. Liver b. Thymus c. Spleen d. Bone marrow

    c. Spleen

  • 100

    What is the principle of mechanical endpoint detection in coagulation instruments: a. Decrease in light transmittance as fibrin forms b. Increase in light absorbance as latex particles coated with sepcific antibody are agglutinated by antigen c. Increase in light absorbance at 405 nm as paranitroaniline is cleaved from synthetic substrate by the coagulation enzyme d. Change in movement of steel ball when clot forms

    d. Change in movement of steel ball when clot forms