Deck 14: The Myelodysplastic Syndromes
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Deck 14: The Myelodysplastic Syndromes
1
All of the following are associated with the development of the MDSs except:
A) Alkylating therapy
B) Benzene exposure
C) Alcoholism
D) Radiation
A) Alkylating therapy
B) Benzene exposure
C) Alcoholism
D) Radiation
C
2
The most common hematological malignancy in the adult population is:
A) Acute leukemia
B) Multiple myeloma
C) Myelodysplastic syndrome
D) Chronic leukemias
A) Acute leukemia
B) Multiple myeloma
C) Myelodysplastic syndrome
D) Chronic leukemias
C
3

The cell at the tip of the pointer is:
A) A basophil
B) A malignant cell
C) A degenerating neutrophil
D) Not a cell; it's an artifact
C
4

The correct name for the cell at the end of the pointer is a:
A) Ringed sideroblast
B) Reticulocyte
C) Giant platelet
D) Siderocyte
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5
Refractory anemia is an anemia that:
A) Has more than 5% blasts in the peripheral blood
B) Is resistant to treatment
C) Will usually demonstrate a hypoplastic bone marrow
D) Demonstrates a 17g deletion routinely
A) Has more than 5% blasts in the peripheral blood
B) Is resistant to treatment
C) Will usually demonstrate a hypoplastic bone marrow
D) Demonstrates a 17g deletion routinely
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6
The bone marrow and peripheral smear of a patient with an MDS will show dysplastic changes in _over time.
A) white cells
B) red cells
C) platelets
D) All of the above
A) white cells
B) red cells
C) platelets
D) All of the above
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7

The cell at the tip of the pointer is a:
A) Hairy cell
B) Basket cell
C) Degenerating lymphocyte
D) Giant platelet
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8
All of the following are features of the myelodysplastic syndromes except:
A) Anemia
B) Organomegaly
C) Dysplasia
D) Hypercellular marrow
A) Anemia
B) Organomegaly
C) Dysplasia
D) Hypercellular marrow
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9
One of the key white cell features in MDS is:
A) Hypersegmented neutrophils
B) Auer rods
C) Dohle bodies
D) Pseudo Pelger-Huët
A) Hypersegmented neutrophils
B) Auer rods
C) Dohle bodies
D) Pseudo Pelger-Huët
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10
Which of the following bone marrow blast percentages will be consistent with the FAB classification of refractory anemia with excess of blasts (RAEB)?
A) 5% to 20%
B) 20% to 30%
C) Greater than 30%
D) Less than 5%
A) 5% to 20%
B) 20% to 30%
C) Greater than 30%
D) Less than 5%
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11
The most effective means of treating iron overload in the myelodysplastic syndromes is:
A) Therapeutic phlebotomy
B) Limiting iron-containing foods
C) Iron chelation therapy
D) Fasting
A) Therapeutic phlebotomy
B) Limiting iron-containing foods
C) Iron chelation therapy
D) Fasting
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12
A large percentage of the MDSs end in an acute leukemia.
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13
Reticulocytopenia is a feature of MDS.Which one of the following is the mechanism behind this process?
A) Heavy tumor burden
B) Marrow aplasia
C) Ineffective erythropoiesis
D) Toxic effects
A) Heavy tumor burden
B) Marrow aplasia
C) Ineffective erythropoiesis
D) Toxic effects
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14
The FAB classification of the MDSs include CML.
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15
The blast count in most individuals with MDS is:
A) Less than 10%
B) Less than 40%
C) Less than 5%
D) Less than 20%
A) Less than 10%
B) Less than 40%
C) Less than 5%
D) Less than 20%
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16
Typically, patients with MDS will exhibit partial or complete absence of:
A) Chromosomes 5 and 7
B) Chromosomes 8 and 12
C) The Y chromosome
D) Dysplasia
A) Chromosomes 5 and 7
B) Chromosomes 8 and 12
C) The Y chromosome
D) Dysplasia
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17
Deleted 5q MDS is primarily seen in male patients.
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18
The morphological classification of anemia in the myelodysplastic syndromes is:
A) Normocytic, normochromic
B) Microcytic, hypochromic
C) Macrocytic, normochromic
D) Microcytic, normochromic
A) Normocytic, normochromic
B) Microcytic, hypochromic
C) Macrocytic, normochromic
D) Microcytic, normochromic
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19
Which of the following chromosome disorders in MDS has a poor predictive influence?
A) Chromosome 7 disorder
B) Trisomy 12
C) Trisomy 13
D) 17q deletion
A) Chromosome 7 disorder
B) Trisomy 12
C) Trisomy 13
D) 17q deletion
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20
All of the following are dysplastic changes of platelets frequently seen in MDS except:
A) Abnormal granulation
B) Micromega karyocytes
C) Giant platelets
D) Platelet satellitism
A) Abnormal granulation
B) Micromega karyocytes
C) Giant platelets
D) Platelet satellitism
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