Deck 9: The Hematopoietic and Lymphoid System
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Deck 9: The Hematopoietic and Lymphoid System
1
The diagnostic feature of multiple myeloma is best documented by:
A) Peripheral blood smear analysis
B) Serum electrophoresis
C) Measurement of serum osmolarity
D) Measurement of serum calcium
E) Molecular biology
A) Peripheral blood smear analysis
B) Serum electrophoresis
C) Measurement of serum osmolarity
D) Measurement of serum calcium
E) Molecular biology
Serum electrophoresis
2
The most common symptom of lymphomas is:
A) Lymph node enlargement
B) Infection
C) Fever
D) Pruritus
E) Sweating
A) Lymph node enlargement
B) Infection
C) Fever
D) Pruritus
E) Sweating
Lymph node enlargement
3
All of the following findings are typical of secondary polycythemia except:
A) Increased number of red blood cells in circulation
B) Hyperviscosity of the blood
C) Increased number of erythroid precursors in the bone marrow
D) Increased incidence of thrombi
E) Association with myelodysplastic syndromes
A) Increased number of red blood cells in circulation
B) Hyperviscosity of the blood
C) Increased number of erythroid precursors in the bone marrow
D) Increased incidence of thrombi
E) Association with myelodysplastic syndromes
Association with myelodysplastic syndromes
4
Sickle cell hemoglobin is routinely identified in the laboratory by:
A) Polarized light microscopy
B) Electron microscopy
C) Electrophoresis
D) Immunochemistry
E) Electron spin microscopy
A) Polarized light microscopy
B) Electron microscopy
C) Electrophoresis
D) Immunochemistry
E) Electron spin microscopy
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5
Which leukemia has the best prognosis without chemotherapy?
A) Acute lymphoblastic leukemia
B) Acute myelogenous leukemia
C) Chronic lymphocytic leukemia
D) Chronic myelogenous leukemia
E) Plasma cell leukemia
A) Acute lymphoblastic leukemia
B) Acute myelogenous leukemia
C) Chronic lymphocytic leukemia
D) Chronic myelogenous leukemia
E) Plasma cell leukemia
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6
All of the following are hemolytic anemias caused by red blood cell abnormalities (intracorpuscular defects)except:
A) Sickle cell anemia
B) Hereditary spherocytosis
C) Thalassemia major
D) Thalassemia minor
E) Autoimmune hemolytic anemia
A) Sickle cell anemia
B) Hereditary spherocytosis
C) Thalassemia major
D) Thalassemia minor
E) Autoimmune hemolytic anemia
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7
The most common form of leukemia in children younger than 5 years is:
A) Acute lymphoblastic leukemia
B) Acute myelogenous leukemia
C) Chronic lymphocytic leukemia
D) Chronic myelogenous leukemia
E) Plasma cell leukemia
A) Acute lymphoblastic leukemia
B) Acute myelogenous leukemia
C) Chronic lymphocytic leukemia
D) Chronic myelogenous leukemia
E) Plasma cell leukemia
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8
Aplastic anemia is most often:
A) Idiopathic
B) Secondary to viral infection
C) Radiation induced
D) Drug induced
E) Immune mediated
A) Idiopathic
B) Secondary to viral infection
C) Radiation induced
D) Drug induced
E) Immune mediated
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9
Fibrin split products are typically found in the urine of patients who have:
A) Hemophilia A
B) Hemophilia B
C) Disseminated intravascular coagulation (DIC)
D) Aplastic anemia
E) Thrombocytopenia
A) Hemophilia A
B) Hemophilia B
C) Disseminated intravascular coagulation (DIC)
D) Aplastic anemia
E) Thrombocytopenia
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10
Punched-out bone lesions of the calvaria seen by x-ray examination are typical of:
A) Hodgkin's disease
B) Thrombotic thrombocytopenic purpura
C) Multiple myeloma
D) Aplastic anemia
E) Lymphocytic lymphoma
A) Hodgkin's disease
B) Thrombotic thrombocytopenic purpura
C) Multiple myeloma
D) Aplastic anemia
E) Lymphocytic lymphoma
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11
Microcytic hypochromic anemia with low hemosiderin stores in the bone marrow responds favorably to treatment with:
A) Vitamin C
B) Vitamin B12
C) Folic acid
D) Iron
E) Selenium
A) Vitamin C
B) Vitamin B12
C) Folic acid
D) Iron
E) Selenium
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12
Overall,the most common form of leukemia is:
A) Acute lymphoblastic leukemia
B) Acute myelogenous leukemia
C) Chronic lymphocytic leukemia
D) Chronic myelogenous leukemia
E) Plasma cell leukemia
A) Acute lymphoblastic leukemia
B) Acute myelogenous leukemia
C) Chronic lymphocytic leukemia
D) Chronic myelogenous leukemia
E) Plasma cell leukemia
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13
Epstein-Barr virus,a possible cause of Burkitt's lymphoma,has a predilection for infecting:
A) T-suppressor/cytotoxic lymphocytes
B) T-helper lymphocytes
C) Plasma cells
D) B lymphocytes
E) Eosinophils
A) T-suppressor/cytotoxic lymphocytes
B) T-helper lymphocytes
C) Plasma cells
D) B lymphocytes
E) Eosinophils
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14
Which lymphoma is classified as a low-grade lymphoma?
A) Follicular lymphoma
B) Diffuse large-cell lymphoma
C) Burkitt's lymphoma
D) Immunoblastic lymphoma
E) Lymphoblastic lymphoma
A) Follicular lymphoma
B) Diffuse large-cell lymphoma
C) Burkitt's lymphoma
D) Immunoblastic lymphoma
E) Lymphoblastic lymphoma
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15
The sickling of red blood cells of patients with sickle cell anemia can be induced in a test tube by exposing the blood to:
A) Normal blood
B) Normal serum
C) Oxygen
D) An oxygen-binding chemical such as metabisulfite
E) Alkali
A) Normal blood
B) Normal serum
C) Oxygen
D) An oxygen-binding chemical such as metabisulfite
E) Alkali
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16
Which virus is a proven cause of leukemia/lymphoma in humans?
A) Epstein-Barr virus
B) HIV
C) HTLV-1
D) HPV
E) CMV
A) Epstein-Barr virus
B) HIV
C) HTLV-1
D) HPV
E) CMV
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17
Thalassemia minor is a disease involving the gene that encodes:
A) Globin chains of hemoglobin
B) The heme portion of hemoglobin
C) The iron-binding portion of hemoglobin
D) The porphyrin ring of hemoglobin
E) Bilirubin synthetase
A) Globin chains of hemoglobin
B) The heme portion of hemoglobin
C) The iron-binding portion of hemoglobin
D) The porphyrin ring of hemoglobin
E) Bilirubin synthetase
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18
Which vitamin is necessary for the liver to synthesize clotting factors: II,VII,IX,and X?
A) Vitamin B12
B) Vitamin B6
C) Vitamin K
D) Vitamin C
E) Vitamin D
A) Vitamin B12
B) Vitamin B6
C) Vitamin K
D) Vitamin C
E) Vitamin D
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19
Macrocytic,megaloblastic anemia occurs typically in association with:
A) Chronic dermatitis
B) Atrophic gastritis
C) Hypothyroidism
D) Old age
E) Chronic osteoarthritis
A) Chronic dermatitis
B) Atrophic gastritis
C) Hypothyroidism
D) Old age
E) Chronic osteoarthritis
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20
Consumption of platelets associated with widespread hemorrhages is a feature of:
A) Hemophilia A
B) Hemophilia B
C) Aplastic anemia
D) Leukemia
E) Disseminated intravascular coagulation (DIC)
A) Hemophilia A
B) Hemophilia B
C) Aplastic anemia
D) Leukemia
E) Disseminated intravascular coagulation (DIC)
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