Professional Documents
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24. Which of the following organs is responsible for the “pitting process” for RBCs?
a. liver b. spleen c. kidney d. lymph nodes
25. Which of the following disorders has an increase in osmotic fragility?
a. iron deficiency anemia c. hereditary stomatocytosis
b. hereditary elliptocytosis d. hereditary spherocytosis
26. What is the major hemoglobin found in the RBCs of patients with sickle cell trait?
a. hgb S b. hgb F c. hgb A2 d. Hgb A
27. Select the amino acid substitution that is responsible for sickle cell anemia?
a. lysine is substituted for glutamic acid at the sixth position of the alpha chain
b. valine is substituted for glutamic acid at the sixth position of the beta chain
c. valine is substituted for glutamic acid at the sixth position of the alpha chain
d. glutamine is substituted for glutamic acid at the sixth position of the beta chain
28. All of the following are usually found in hemoglobin C disease, except:
a. Hemoglobin C crystals c. lysine substituted for glutamic acid at sixth position of β-chain
b. Target cells d. fast mobility of hemoglobin C at pH 8.6
29. Which of the following hemoglobins migrates to the same position as hgb A2 at pH 8.6?
a. hgb H b. hgb F c. hgb C d. hgb S
30. Which of the following electrophoretic results is consistent with a diagnosis of sickle cell trait?
a. hgb A: 40%, hgb S 35%, hgb F 5% c. hgb A: 0%, hgb A2 5%, hgb F 95%
b. hgb A: 60%, hgb S 40%, hgb A2 2% d. hgb A: 80%, hgb S 10%, hgb A2 10%
31. Which of the following is true of paroxysmal nocturnal hemoglobinuria (PNH)?
a. it is an acquired hemolytic anemia c. it is inherited as an autosomal dominant trait
b. it is inherited as a sex-linked trait d. it is inherited as an autosomal recessive trait
32. Hemolytic uremic syndrome (HUS) is characterized by all of the following, except:
a. hemorrhage b. thrombocytopenia c. hemoglobinuria d. reticulocytopenia
33. An autohemolysis test is positive in all of the following except:
a. G6PD deficiency b. HS c. pyruvate kinase deficiency d. PNH
34. Which antibody is associated with paroxysmal cold hemoglobinuria (PCH)?
a. anti-I b. anti-i c. anti-M d. anti-P
35. All of the following are associated with hemolytic anemia except:
a. methemoglobinemia c. hemoglobinemia
b. hemoglobinuria d. increased haptoglobin
36. Bite cells are usually seen in patients with:
a. Rh null trait b. CGD c. G6PD deficienct d. PK deficiency
37. The morphological classification of anemias is based on which of the following?
a. M:E ratio b. Prussian blue stain c. RBC indices d. reticulocyte count
38. Microangioathic hemolytic anemia is characterized by:
a. target cells and Cabot rings c. Pappenheimer bodies and basophilic stipplings
b. toxic granules and Dohle bodies d. schistocytes and nucleated RBCs
39. Which antibiotic is most often implicated in the development of aplastic anemia?
a. sulfonamides b. penicillin c. tetracycline d. chloramphenicol
40. Which of the following conditions may produce spherocytes in a peripheral smear?
a. Pelger-Huet anomaly c. autoimmune hemolytic anemia
b. perncious anemia d. sideroblastic anemia
41. Reticulocytosis usually indicates:
a. response to inflammation c. aplastic anemia
b. neoplastic process d. red cell regeneration
42. The OFT result in a patient with thalassemia major would most likely be:
a. increased b. decreased c. normal d. all of these
43. Iron deficiency anemia may be distinguished from anemia of chronic infection by:
a. serum iron level c. red cell indices
b. red cell morphology d. total iron binding capacity
44. Which anemia has red cell morphology similar to that seen in IDA?
a. sickle cell anemia b. thalassemia syndrome c. pernicious anemia d. HS
45. Which morphological classification is characteristic of megaloblastic anemia?
a. normocytic, normochromic c. macrocytic, hypochromic
b. microcytic, normochromic d. macrocytic, normochromic
46. All of the following are characteristics of megaloblastic anemia except:
a. pancytopenia c. hypersegmented neutrophil
b. elevated reticulocyte count d. macrocytic erythrocyte indices
47. Which of the disorders below causes ineffective erythropoiesis?
a. G6PD deficiency b. liver disease c. Hgb C disease d. pernicious anemia
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48. Which of the following may be seen in the peripheral blood smear of a patient with obstructive liver disease?
a. schistocytes b. macrocytes c. Howell-Jolly bodies d. microcytes
49. The macrocytes typically seen in megaloblastic processes are:
a. creascent-shaped b. teardrop-shaped c. ovalocytic d. pencil-shaped
50. Which inclusions may be seen in leukocytes?
a. Dohle bodies b. basophilic stippling c. malarial parasite d. Howell-Jolly bodies
51. Which of the following is contained in the primary granules of the neutrophil?
a. lactoferrin b. myeloperoxidase c. histamine d. alkaline phosphatase
52. The morphological characteristic associated with Chediak-Higashi syndrome is:
a. pale blue cytoplasmic inclusiosns c. small, dark staining granules and condensed nuclei
b. giant lysosomal granules d. nuclear hyposegmentation
53. Auer rods may be seen in all of the following except:
a. acute myelomonocytic leukemia (M4) c. acute myeloid leukemia without maturation (M1)
b. acute lymphoblastic leukemia d. acute promyelocytic leukemia (M3)
54. Which type of anemia is usually present in a patient with acute leukemia?
a. microcytic, hyperchromic c. normocytic, normochromic
b. microcytic, hypochromic d. macrocytic, normochromic
55. In leukemia, which term describes a peripheral blood finding of leukocytosis with a shift to the left, accompanied by
occasional nucleated red cells?
a. megaloblastosis b. dysplasia c. leukoerythroblastosis d. none of these
56. DIC is most often associated with which of the following types of acute leukemia?
a. acute myeloid leukemia without maturation c. acute myelomonocytic leukemia
b. acute promyelocytic leukemia d. acute monocytic leukemia
57. A peripheral smear shows 75% blasts. These stain positive for both Sudan black B (SBB) and peroxidase (Px). Given
these values, which of the following disorders is most likely?
a. AML b. CML c. AUL d. ALL
58. Sodium fluoride may be added to the naphthyl ASD acetate (NASDA) esterase reaction. The fluoride is added to
inhibit a positive reaction with:
a. megakaryocytes b. monocytes c. erythrocytes d. granulocytes
59. In essential thrombocythemia, the platelets are:
a. increased in number and functionally abnormal c. decreased number and functional
b. normal in number and functionally abnormal d. decreased in number and functionally abnormal
60. Which of the following cells is considered pathognomonic for Hodgkin’s disease?
a. Niemann-Pick cells b. reactive lymphocytes c. flame cells d. Reed-Sternberg cells
61. In myelofibrosis, the characteristic abnormal red blood cell morphology is that of:
a. target cells b. schistocytes c. teardrop cells d. ovalocytes
62. PV is characterized by:
a. increased plasma volume c. decreased oxygen saturation
b. pancytopenia d. absolute increase in total red cell mass
63. The erythrocytosis seen in relative polycythemia occurs because of:
a. decreased arterial oxygen saturation c. increased erythropoietin levels
b. decreased plasma volume of circulating blood d. increased erythropoiesis in the bone marrow
64. The leukocyte alkaline phosphatase stain of a patient gives the following results: 10 (0); 48(1+); 38(2+); 3(3+); 1(4+).
Calculate the LAP score:
a. 100 b. 117 c. 137 d. 252
65. CML is distinguished from leukomoid reaction by which of the following?
a. CML low LAP; leukomoid high LAP c. CML high WBC; leukomoid normal WBC
b. CML high LAP; leukomoid low LAP d. CML high WBC; leukomoid high WBC
66. What influence does the Philadelphia chromosome have on the prognosis of patients with chronic myelocytic
leukemia?
a. it is not predictive c. prognosis is worse is Ph1 is present
b. prognosis is better if Ph1 is present d. disease usually transforms into AML when Ph1 is present
67. What is the characteristic finding is seen in the peripheral smear of a patient with multiple myeloma?
a. microcytic hypochrmic cells c. rouleaux
b. intracellular inclusion bodies d. hypersegmented neutrophils
68. In which of the following conditions does LAP show the least activity?
a. leukomoid recations b. idiopathic myelofibrosis c. PV d. CML
69. Cells that exhibit a positive stain with acid phosphatase and are not inhibited with tartaric acid are characteristically
seen in:
a. infectious mononucleosis c. hairy cell leukemia
b. infectious lymphocytosis d. T-cell acute lymphoblastic leukemia
70. The anticoagulant of choice for most routine coagulation studies is:
a. sodium oxalate b. sodium citrate c. EDTA d. heparin
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94. Normal PT and APTT results in a patient with poor wound healing may be associated with:
a. factor VII deficiency b. factor VIII deficiency c. factor XII deficiency d. factor XIII deficiency
95. The lupus anticoagulant is directed against:
a. factor VIII b. factor IX c. factor X d. phospholipid
96. What test is used to monitor heparin therapy?
a. INR b. APTT c. PT d. none of these
97. What test is commonly used to monitor warfarin therapy?
a. INR b. APTT c. TT d. BT
98. Which clotting factors (cofactors) are inhibited by protein S?
a. V and X b. Va and VIIIa c. VIII and IX d. VIII and X
99. Which of the following tests is most likely to be abnormal in patients taking aspirin?
a. platelet morphology b. platelet count c. bleeding time d. prothrombin time
100. A prolonged thrombin time and a normal reptilase time are indicative of:
a. afibrinogenemia b. hypofibrinogenemia c. aspirin therapy d. heparin therapy
56. Which of the following is an acquired red cell membrane defect that result in increased sensitivity to complement
binding?
A. March hemoglobinuria C. Paroxysmal cold hemoglobinuria
B. Paroxysmal nocturnal hemoglobinuria D. Methemoglobinemia
57. An increase in erythropoietin is NOT a normal compensating mechanism in which of the following conditions?
A. Renal tumors C. Cardiovascular disease
B. Heavy smoking D. Pulmonary disease
58. The LAP activity will usually be increased in:
1. Chronic myelogenous leukemia 3. Paroxysmal nocturnal hemoglobinuria
2. Third trimester of pregnancy 4. Polycythemia vera
A. 1, 2 and 3 C. 2 and 4
B. 1 and 3 D. Only 4
59. In differentiating a neutrophilic leukomoid reaction from chronic granulocytic leukemia, which of the following is(are)
helpful:
1. LAP score 3. Chromosome studies
2. Bone marrow cellularity 4. Sudan black stain
A. 1, 2 and 3 C. 2 and 4
B. 1 and 3 D. Only 4
60. The neutrophil mitotic pool includes:
1. Promyelocytes 3. Myelocytes
2. Myeloblasts 4. Metamyelocytes
A. 1, 2 and 3 C. 2 and 4
B. 1 and 3 D. Only 4
61. The neutrophil post-mitotic pool includes:
1. Promyelocytes 3. Myelocytes
2. Metamyelocytes 4. Bands
A. 1, 2 and 3 C. 2 and 4
B. 1 and 3 D. Only 4
62. FAB classification of myelodysplastic syndrome (MDS) includes:
1. Refractory anemia 3. Refractory anemia with excess blasts
2. Refractory anemia with ringed sideroblasts 4. Chronic myelomonocytic leukemia
A. 1 and 3 C. 1, 2 and 3
B. 2 and 4 D. 1, 2, 3 and 4
63. Tartrate-resistant acid phosphatase (TRAP) activity is diagnostic of:
1. Acute lymphoblastic leukemia 3. Chronic lymphocytic leukemia
2. Hodgkin’s lymphoma 4. Hairy cell leukemia
A. 1, 2 and 3 C. 2 and 4
B. 1 and 3 D. Only 4
64. The most mature granulocyte precursor that can undergo mitosis is the:
A. Myeloblast C. Myelocyte
B. Promyelocyte D. Metamyelocyte
65. Vasodilation and bronchostriction are the result of dgranulation by which of the following blood cells?
A. Eosinophils C. Neutrophils
B. Monocytes D. Basophils
66. In patients with infectious mononucleosis, which blood cells are infected by the causative agent?
A. Monocytes C. B lymphocytes
B. T lymphocytes D. Histiocytes
67. In which of the following are eosinophils NOT increased?
A. Cushing syndrome C. Skin disorders
B. Allergic disorders D. Parasitic infection
68. A Gaucher cell is best described as a macrophage with:
A. Wrinkled cytoplasm due to an accumulation of glucocerebroside
B. Foamy cytoplasm filled with unmetabolized sphingomyelin
C. Pronounced vacuolization and deposits of cholesterol
D. Abundant cytoplasm containing storage iron and cellular remnants
69. Which of the following is NOT classified as a myeloproliferative disorder?
A. Polycythemia vera C. Multiple myeloma
B. Essential thromcythemia D. Chronic myelogenous leukemia
70. In which of the following would an absolute monocytosis NOT seen?
A. Tuberculosis C. Collagen disorders
B. Infectious mononucleosis D. Recovery stage of acute bacterial infection
71. Alder-Reilly anomaly is an abnormality of:
A. Lysosomal fusion C. Oxidative metabolism
B. Nuclear maturation D. Mucopolysaccharide metabolism
72. What is the key diagnostic test for Hodgkin lymphoma?
A. Bone marrow biopsy C. Spinal tap
B. Lymph node biopsy D. Skin biopsy
73. The presence of both immature neutrophils and nucleated erythrocytes in the peripheral blood is most accurately
called:
A. Neutrophilic left shift C. Neutrophilic leukomoid reaction
B. Regenerative left shift D. Leukoerythroblastic reaction
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93. What influence does the Philadelphia (Ph1) chromosome have on the prognosis of patients with chronic myelocytic
leukemia?
A. It is not predictive C. The prognosis is worse if Ph1 is present
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B. The prognosis is better if Ph is present D. The disease usually transforms into AML when Ph1 is
94. Laboratory findings in hereditary spherocytosis do NOT include:
A. Decreased osmotic fragility C. Reticulocytosis
B. Increased autohemolysis corrected by glucose D. Shortened erythrocyte survival
95. The laboratory findings on a patient are as follows:
MCV 55fL MCHC 25% MCH 17 pg
A stained blood film of this patient would most likely reveal a red cell picture that is:
A. Microcytic, hypochromic C. Normocytic, normochromic
B. Macrocytic, hypochromic D. Microcytic, normochromic
96. Which of the following laboratory findings is associated with Factor XIII deficiency?
A. Prolonged activated partial thromboplastin time C. Prolonged thrombin time
B. Clot solubility in a 5 molar urea solution D. Prolonged prothrombin time
97. Which test would be abnormal in patient with Stuart-Prower factor (factor X) deficiency?
A. PT only C. APTT only
B. PT and APTT D. Thrombin time
98. Aspirin prevents platelet aggregation by inhibiting the action of which enzyme?
A. Phospholipase C. Cyclooxygenase
B. Thromboxane A2 synthetase D. Prostacyclin synthetase
99. Which of the following is most likely to be abnormal in patients taking aspirin?
A. Platelet morphology C. Platelet count
B. Bleeding time D. Prothrombin time
100. Which results are associated with Hemophilia A?
A. Prolonged APTT, normal PT C. Prolonged PT, normal APTT
B. Prolonged PT and APTT D. Normal PT and APTT
23. Many microspherocytes and schistocytes and budding off of spherocytes can be seen on peripheral blood
smears of patients with:
a. hereditary spherocytosis c. acquired autoimmune hemolytic anemia
b. disseminated intravascular coagulation (DIC) d. extensive burns
24. Which of the following is most likely to be seen in lead poisoning?
a. iron overload in tissue b. codocytes c. basophilic stippling d. ringed sideroblasts
25. What cell shape is MOST commonly associated with an increased MCHC?
a. teardrop cells b. target cells c spherocytes d. sickle cells
26. Microangiopathic hemolytic anemia is characterized by:
a. Target cells and Cabot rings c. Pappenheimer bodies and basophilic stipplings
b. Toxic granules and Dohle bodies d. Schistocytes and nucleated RBCs
27. In myelofibrosis, the characteristic abnormal red cell morphology is:
a. Target cells b. Schistocytes c. Teardrop cells d. Ovalocytes
28. An enzyme deficiency associated with a moderate to severe hemolytic anemia after the patient is exposed to
certain drugs and that is characterized by red cell inclusions formed by denatured hemoglobin is:
a. lactate dehydrogenase deficiency c. pyruvate kinase deficiency
b. G-6-PD deficiency d. hexokinase deficiency
29. A 15-year-old girl is taking primaquine for a parasitic infection and notices her urine is a brownish color. A CBC
shows mild anemia. The laboratorian performing the reticulocyte count notices numerous irregular shaped
granules near the periphery of the RBC. These cellular inclusions are most likely:
a. Howell-Jolly bodies b. basophilic stippling c. Heinz bodies d. Pappenheimer bodies
30. What primary defect does the amino acid substitution in the -chain of Hb S have on the hemoglobin molecule?
a. Increases its oxygen affinity c. Decreases its solubility
b. Alters its stability d. Increases its solubility
31. Which of the following hemoglobin electrophoresis results is most typical of sickle cell trait?
a. 85% HbS and 15% HbA c. 45% HbS and 55% HbA
b. 85% HbF and 15% HbS d. 55% HbF and 45% HbS
32. What is the pathophysiology of β-thalassemia?
a. Decreased synthesis of α- chains c. Synthesis of structurally abnormal β-chains
b. Decreased synthesis of β-chains d. Abnormal heme synthesis
33. Iron deficiency anemia may be distinguished from anemia of chronic infection by:
a. Serum iron level b. Red cell morphology c. Red cell indices d TIBC
34. Which antibiotic is most often implicated in the development of aplastic anemia?
a. Sulfonamides b. Chloramphenicol c. Teracycline d. Penicillin
35. Which of the following is a pure red cell aplasia?
a. Bernard-Soulier syndrome c. Diamond-Blackfan anemia
b. DiGuglielmo’s disease d. Fanconi’s anemia
36. Spherocytes may be seen in the peripheral blood of patients with:
a. Autoimmune hemolytic anemia c. Iron deficiency anemia
b. Vitamin B12 deficiency d. Pyruvate kinase deficiency
37. In a jaundiced 16-year-old, laboratory studies indicate that the MCHC is increased, the Coombs' test is
negative, and osmotic fragility of the red cells is increased. Erythrocytes on a peripheral smear are most likely
to be:
a. Acanthocytes b. Spherocytes c. Teardrop cells d. Target cells
38. Which of these hemoglobin derivatives cannot be reduced back to normal hemoglobin?
a. Methemoglobin b. Oxyhemoglbin c. Sulfhemoglobin d. Carboxyhemoglobin
39. Which of the following is associated with Chediak-Higashi syndrome?
a. membrane defect of lysosomes c. two-lobed neutrophils
b. Dohle bodies and giant platelets d. mucopolysaccharidosis
40. Which of the following is associated with Alder-Reilly inclusions?
a. membrane defect of lysosomes c. two-lobed neutrophils
b. Dohle bodies and giant platelets d. mucopolysaccharidosis
41. A differential was performed on an asymptomatic patient. The differential included 60% neutrophils: 55 of
which had 2 lobes and 5 had 3 lobes. There were no other abnormalities. This is consistent with which of the
following anomalies?
a. Pelger-Huet b. May-Hegglin c. Alder-Reilly d. Chediak-Higashi
42. Of the following, the disease most closely associated with pale blue inclusions in granulocytes and giant
platelets is:
a. Gaucher’s disease b. May-Hegglin anomaly c. Alder-Reilly anomaly d. Pelger-Huet anomaly
43. Of the following, the disease most closely associated with glucocerebrosidase deficiency is:
a. Gaucher’s disease b. Pelger-Huet anomaly c. Chediak-Higashi syndrome d. May-Hegglin anomaly
44. Bone marrow slide shows foam cells ranging from 20 to 100 m in size with vacuolated cytoplasm containing
sphingomyelin and is faintly PAS positive. This cell type is most characteristic of:
a. Gaucher’s disease b. Di Guglielmo disease c. myeloma with Russell bodies d. Niemann-Pick disease
45. In the French-American-Bristish (FAB) classification, myelomonocytic leukemia would be:
a. M1 and M2 b. M3 c. M4 d. M5
46. DIC is most often associated with which of the following FAB designation of acute leukemia?
a. M1 b. M3 c. M4 d. M5
47. Auer rods are most likely present in which of the following?
a. chronic granulocytic leukemia c. erythroleukemia
b. myelofibrosis with myeloid metaplasia d. acute granulocytic leukemia
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48. Which of the following stains is helpful in the diagnosis of suspected erythroleukemia?
a. peroxidase b. periodic acid-Schiff c. nonspecific esterase d. acid phosphatase
49. The FAB classification of ALL seen most commonly in children is:
a.L1 b. L2 c. L3 d. Burkitt’s type
50. A 50-year-old woman who has been receiving busulfan for 3 years for chronic myelogenous leukemia becomes
anemic. Laboratory tests reveal:
Thrombocytopenia
Many peroxidase-negative blast cells in the peripheral blood
Bone marrow hypercellular in blast transformation
Markedly increased bone marrow TdT
Which of the following complications is this patient most likely to have?
a. acute lymphocytic leukemia c. acute myelomonocytic leukemia
b. acute myelocytic leukemia d. busulfan toxicity
51. A peripheral smear shows 75% blasts. These stain positive for SBB and peroxidase. Given these values, which
of the following disorders is most likely?
a. AML b. CML c. Undiff.leukemia d. ALL
52. A peripheral blood smear demonstrating an absolute increase in small “hypermature” lymphocytes and
“smudge” cells would be suggestive of:
a. Chronic lymphocytic leukemia c. Leukomoid reaction
b. Acute lymphocytic leukemia d. Infectious mononucleosis
53. Chromosome analysis revealed the presence of the Philadelphia chromosome. Based on this information, what
myeloproliferative disorder is present?
a. CML b. PV c. ET d. MMM
54. The absence of the Philadelphia chromosome in granulocytic leukemia suggests:
a. Rapid progression of the disease c. Excellent response to therapy
b. Polyclonal origin to the disease d. Conversion to another myeloproloferative disorder
55. Which of the following tests can be useful in differentiating leukemoid reactions from chronic granulocytic
leukemias?
a. peroxidase stain b. surface membrane markers c. Sudan black B stain d. LAP
56. The following results were obtained on a leukocyte alkaline phosphatase stain:
Score 4+ 3+ 2+ 1+ 0
No. of cells counted 40 30 20 5 5
These reactions are most consistent with:
a. leukemoid reaction c. chronic granulocytic leukemia
b. nephrotic syndrome d. progressive muscular dystrophy
57. The esterase cytochemical stains are useful to differentiate:
a. Granulocytic from monocytic leukemias
b. Lymphocytic leukemias from myelocytic leukemias
c. Monocytic leukemias from megakaryocytic leukemias
d. Lymphocytic leukemias from monocytic leukemias
58. The FAB classification of a leukemia with large blasts that are myeloperoxidase and specific esterase negative
but have strong Positivity for nonspecific esterase inhibited by sodium fluoride is:
a. M1 b. M4 c. M5 d. M7
59. Which of the following cells are most likely identified in lesions of mycosis fungoides?
a. T lymphocytes b. B lymphocytes c. monocytes d. mast cells
60. The atypical lymphocyte seen in the peripheral smear of patients with infectious mononucleosis is reacting to
which of the following?
a. T lymphocytes b. B lymphocytes c. monocytes d. mast cells
61. Which of the following cells are the atypical lymphocytes seen on the peripheral blood smear of patients with
infectious mononucleosis?
a. T lymphocytes b. B lymphocytes c. monocytes d. mast cells
62. The results of a bone marrow differential are: 40% neutrophils and precursors; 20% lymphocytes, 20%
monocytes, and 20% red cell precursors. The M;E ratio for this patient is:
a. 1:2 b. 2:1 c. 3:1 d. 4:1
63. When Reed-Sternberg cells are found in a lymph node biopsy, they are indicative of:
a. Hodgkin disease c. Sezary syndrome
b. Intermediate-grade non-Hodgkin lymphoma d. High-grade non-Hodgkin lymphoma
64. The antigen referred to as CALLA, the common ALL antigen is:
a. CD 10 b. CD 16 c. CD 56 d. CD 73
65. Normal platelets have a circulating life span of approximately:
a. 5 days b. 10 days c. 20 days d. 30 days
66. Platelet dense granules contain:
1. Calcium 2. Storage ADP 3. Serotonin 4. Plt factor 4
a. 1 and 3 b. 2 and 4 c. 1, 2 and 3 d. 1, 2, 3 and 4
67. The type of microscopy recommended for a manual platelet count is:
a. Fluorescence b. Phase c. Brightfiled d. Oil immersion
68. Which of the following is characteristic of Bernard-Soulier syndrome?
a. giant platelets c. abnormal aggregation with ADP
b. normal bleeding time d. increased platelet count
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92. The observation of a normal reptilase time and a prolonged thrombin time is indicative of:
a. Presence of fibrin degradation products c. Dysfibrinogenemia
b. Hypoplasminogenemia d. Presence of heparin
93. When making a blood film using the spreader slide technique, a thinner film can be obtained by:
a. Increasing the angle of the spreader slide c. Spreading the blood at lower speed
b. Using a larger drop of blood d. All of the above
94. A false increase in ESR value can be caused by:
a. Cold room temperatures c. Reading ESR after exactly 30 minutes
b. Slight tilting of the ESR tube rack d. Overanticoagulation of the blood specimen
95. Which of the following statements concerning reticulocyte count is/are true?
1. The adult reference range is approximately 0.5 to 5.0%
2. Newborns have a higher reference range than adults
3. The material that stains in reticulocytes is DNA
4. The Miller disk is a device used to aid in reticulocyte counting
a. 1 and 3 b. 2 and 4 c. 1, 2 and 3 d. 4 only
96. In an automated instrument, which parameter is calculated rather than directly measured:
a. Hematocrit b. RBC count c. WBC count d. Hemoglobin
97. The cyanmethemoglobin method measures:
a. All hemoglobin pigments c. All hemoglobin pigments except sulfhemoglobin
b. Only oxyhemoglobin d. Only methemoglobin
98. Two hemoglobins that migrate together on cellulose acetate electrophoresis at an alkaline pH are:
a. A1 and A2 b. A1 and E c. S and C d. S and D
99. A decreased result in the osmotic fragility test would be associated with which of the following conditions?
a. Sickle cell anemia b. H. spherocytosis c. HDN d. AIHA
100. A patient has the following results: erythrocyte count, 2.5 x 1012/L, hemoglobin 5.3 g/dL; hematocrit 0.17
L/L; reticulocyte count, 1%. What are the erythrocyte indices in the above patient?
a. MCV 47 MCH 28 MCHC 31 c. MCV 80 MCH 21 MCHC 41
b. MCV 68 MCH 21 MCHC 31 d. MCV 80 MCH 28 MCHC 41