Deck 17: Chronic Myeloproliferative Disorders I: Chronic Myelogenous Leukemia
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Deck 17: Chronic Myeloproliferative Disorders I: Chronic Myelogenous Leukemia
1
The prominent laboratory feature representative of CML is:
A) Leukocytosis with left shift
B) Leukocytosis with megaloblastic anemia
C) Leukopenia with lymphocytosis
D) Leukopenia with reticulocytosis
E) None of the above
A) Leukocytosis with left shift
B) Leukocytosis with megaloblastic anemia
C) Leukopenia with lymphocytosis
D) Leukopenia with reticulocytosis
E) None of the above
Leukocytosis with left shift
2
How is CML differentiated from a leukemoid reaction?
A) WBC >100,000/µL
B) Decreased leukocyte alkaline phosphatase (LAP)
C) Shift to the left
D) Increased LAP
E) RBC indices
A) WBC >100,000/µL
B) Decreased leukocyte alkaline phosphatase (LAP)
C) Shift to the left
D) Increased LAP
E) RBC indices
Decreased leukocyte alkaline phosphatase (LAP)
3
In CML the term "maturation arrest" refers to the:
A) Presence of cellular differentiation beyond the blast stage
B) Absence of cellular differentiation beyond the blast or promyelocyte stage
C) Absence of cellular differentiation beyond the band stage
D) Absence of cellular differentiation beyond the metamyelocyte stage
E) None of the above
A) Presence of cellular differentiation beyond the blast stage
B) Absence of cellular differentiation beyond the blast or promyelocyte stage
C) Absence of cellular differentiation beyond the band stage
D) Absence of cellular differentiation beyond the metamyelocyte stage
E) None of the above
Absence of cellular differentiation beyond the blast or promyelocyte stage
4
Which clinical signs are evident in CML?
A) Splenomegaly
B) Hepatomegaly
C) Pallor
D) Epistaxis
E) All of the above
A) Splenomegaly
B) Hepatomegaly
C) Pallor
D) Epistaxis
E) All of the above
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5
When CML is diagnosed in infants and toddlers, it is called __________ CML.
A) Young
B) Juvenile
C) Infant
D) Myelofibrosis
E) AML
A) Young
B) Juvenile
C) Infant
D) Myelofibrosis
E) AML
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6
Philadelphia chromosome is present in __________ percent of patients with typical leukemia cells.
A) 90-95%
B) 40-50%
C) 40-60%
D) 30-40%
E) 65-75%
A) 90-95%
B) 40-50%
C) 40-60%
D) 30-40%
E) 65-75%
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7
Patients with CML in blast crisis most commonly die of:
A) Therapy related to marrow aplasia
B) Exsanguination
C) Infection
D) Aplasia with myelofibrosis
E) All of the above
A) Therapy related to marrow aplasia
B) Exsanguination
C) Infection
D) Aplasia with myelofibrosis
E) All of the above
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8
Chronic myelocytic leukemia (CML) is characterized by examining the production of __________ and their precursors.
A) Erythrocytes
B) Platelets
C) Granulocytes
D) Lymphocytes
E) None of the above
A) Erythrocytes
B) Platelets
C) Granulocytes
D) Lymphocytes
E) None of the above
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9
In CML, transformation to a more critical phase is evident by the appearance of which cells?
A) Blasts
B) Promyelocytes
C) Myelocytes
D) Bands
E) Metamyelocytes
A) Blasts
B) Promyelocytes
C) Myelocytes
D) Bands
E) Metamyelocytes
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10
Which chromosomal abnormality is associated with CML?
A) Deletion 7
B) Chromosome 5
C) Trisomy 12
D) Philadelphia chromosome
E) None of the above
A) Deletion 7
B) Chromosome 5
C) Trisomy 12
D) Philadelphia chromosome
E) None of the above
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11
The usual objective of therapy for the chronic phase of CML is to:
A) Reduce the proliferating myeloid mass
B) Relieve symptoms of hyperleukocytosis
C) Relieve symptoms of thrombocytosis
D) Relieve symptoms of splenomegaly
E) All of the above
A) Reduce the proliferating myeloid mass
B) Relieve symptoms of hyperleukocytosis
C) Relieve symptoms of thrombocytosis
D) Relieve symptoms of splenomegaly
E) All of the above
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12
What is the etiology of chronic myelogenous leukemia?
A) Increased maturation in the granulocytic series
B) Neoplastic transformation of the hematopoietic pluripotent stem cell
C) Virus mediated
D) Suppression of myelopoiesis by cytokine
E) None of the above
A) Increased maturation in the granulocytic series
B) Neoplastic transformation of the hematopoietic pluripotent stem cell
C) Virus mediated
D) Suppression of myelopoiesis by cytokine
E) None of the above
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13
Which cell types contain the Ph chromosome in patients with CML?
A) Neutrophil
B) Monocyte
C) Erythrocyte
D) Platelet
E) All of the above
A) Neutrophil
B) Monocyte
C) Erythrocyte
D) Platelet
E) All of the above
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14
What is the M/E ratio in patients with CML?
A) 1:10
B) 1:5
C) 10:1
D) 3-4:1
E) 4:1
A) 1:10
B) 1:5
C) 10:1
D) 3-4:1
E) 4:1
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15
Which of the following is not consistent with leukemoid reaction?
A) High WBC count
B) High LAP
C) Toxic granulation of neutrophils
D) Presence of Philadelphia chromosome
E) Associated with a bacterial infection
A) High WBC count
B) High LAP
C) Toxic granulation of neutrophils
D) Presence of Philadelphia chromosome
E) Associated with a bacterial infection
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16
What is the chromosomal abnormality in CML?
A) t(8;14)
B) t(9;22)
C) t(1;12)
D) Trisomy 12
E) t(15;17)
A) t(8;14)
B) t(9;22)
C) t(1;12)
D) Trisomy 12
E) t(15;17)
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17
What is characteristic of the bone marrow morphology in CML?
A) Myeloid hyperplasia
B) Normal M/E ratio
C) Myeloid hypoplasia
D) Hypocellularity
E) Erythroid hyperplasia
A) Myeloid hyperplasia
B) Normal M/E ratio
C) Myeloid hypoplasia
D) Hypocellularity
E) Erythroid hyperplasia
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18
The only curative treatment for CML is __________.
A) Steroids
B) Immunosuppressive drugs
C) Radiation therapy
D) Hematopoietic stem cell transplant (HSCT)
E) Tyrosine kinase
A) Steroids
B) Immunosuppressive drugs
C) Radiation therapy
D) Hematopoietic stem cell transplant (HSCT)
E) Tyrosine kinase
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19
CML can be differentiated from polycythemia vera, essential thrombocythemia, and agnogenic myeloid metaplasia by the presence of __________.
A) Leukocytosis
B) Ph chromosome
C) Splenomegaly
D) Erythrocytosis
E) Thrombocytosis
A) Leukocytosis
B) Ph chromosome
C) Splenomegaly
D) Erythrocytosis
E) Thrombocytosis
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20
Which phase of CML carries the worst prognosis and is generally unresponsive to treatment?
A) Chronic phase
B) Accelerated phase
C) Blast crisis
D) Chemotherapy-resistant phase
E) None of the above
A) Chronic phase
B) Accelerated phase
C) Blast crisis
D) Chemotherapy-resistant phase
E) None of the above
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21
Which phase of CML carries the worst prognosis and is generally unresponsive to treatment?
A) Chronic
B) Accelerated
C) Blast
D) Remission
E) Refractory
A) Chronic
B) Accelerated
C) Blast
D) Remission
E) Refractory
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22
Most patients (85%) are diagnosed in which phase of CML?
A) Chronic
B) Accelerated
C) Blast
D) Remission
E) Refractory
A) Chronic
B) Accelerated
C) Blast
D) Remission
E) Refractory
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23
All of the following are characteristics of chronic leukemias except:
A) Insidious onset
B) Mature leukemia cells
C) Found in adults
D) Found primarily in children
E) Organomegaly
A) Insidious onset
B) Mature leukemia cells
C) Found in adults
D) Found primarily in children
E) Organomegaly
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24
Which of the following myeloproliferative disorders is characterized by a decreased LAP score?
A) PV
B) IMF
C) ET
D) AML
E) CML
A) PV
B) IMF
C) ET
D) AML
E) CML
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