Acute Leukemia Flashcards

1
Q

What does the term “leukemia” mean in Greek?

A) Blood cancer
B) White blood
C) Bone marrow disease
D) Lymph node disorder

A

B) White Blood

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2
Q

What are the two main types of acute leukemia?
A) Lymphoblastic and Myeloblastic
B) Myeloma and Lymphoma
C) Chronic and Acute
D) Hodgkin’s and Non-Hodgkin’s

A

Answer: A) Lymphoblastic and Myeloblastic

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3
Q

Which type of acute leukemia is most common in children?

A) AML
B) CML
C) ALL
D) CLL

A

C) Acute Lymphoblastic Leukemia (ALL)

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4
Q

What is the peak incidence age for ALL in children?

A) Birth to 2 years
B) 2 to 5 years
C) 6 to 12 years
D) 13 to 18 years

A

B) 2-5 yrs. old

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5
Q

What is the complete remission rate of adult ALL patients?

A) 40-50%
B) 60-70%
C) 80-90%
D) 95-100%

A

C) 80-90%

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6
Q

Which symptom is more common in B-ALL than T-ALL?

A) Mediastinal mass
B) Mucocutaneous bleeding
C) Thrombocytopenia
D) Organomegaly

A

Answer: B) Mucocutaneous bleeding

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7
Q

What is the characteristic feature of T-ALL presentation?

A) Splenomegaly
B) Large mediastinal mass
C) Jaundice
D) Kidney failure

A

B) Large mediastinal mass

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8
Q

What is the most common genetic abnormality in T-ALL?

A) BCR-ABL1 mutation
B) NOTCH1 mutation
C) Hyperdiploidy
D) RUNX1 translocation

A

B) NOTCH1 MUTATION

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9
Q

Which translocation is associated with Philadelphia chromosome-positive ALL?

A) t(12;21)
B) t(9;22)
C) t(15;17)
D) t(8;14)

A

Answer: B) t(9;22)

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10
Q

What is the prognosis for Philadelphia chromosome-positive ALL?

A) Excellent
B) Poor
C) Moderate
D) No impact

A

Answer: B) Poor

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11
Q

What does “Hyperdiploidy” in B-ALL mean?

A) Loss of chromosomes
B) Extra chromosomes
C) Gene deletion
D) Normal chromosome count

A

B) Extra chromosomes

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12
Q

Which leukemia subtype is more common in infants and may occur in utero?

A) B-ALL with t(12;21)
B) B-ALL with KMT2A(MLL) rearrangement
C) T-ALL with NOTCH1 mutation
D) AML with PML-RARA translocation

A

Answer: B) B-ALL with KMT2A(MLL) rearrangement

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13
Q

Which subtype of ALL has the best prognosis in children?

A) B-ALL with t(12;21)
B) T-ALL with NOTCH1 mutation
C) Philadelphia chromosome-positive ALL
D) AML with FLT3 mutation

A

Answer: A) B-ALL with t(12;21)

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14
Q

What is the primary method used to distinguish ALL from AML?

A) Morphology
B) Immunophenotyping
C) Genetic analysis
D) Blood smear

A

B) Immunophenotyping

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15
Q

What cell surface markers are found in T-ALL?

A) CD19, CD22
B) CD2, CD3, CD4, CD7, CD8
C) CD10, CD34
D) CD5, CD23

A

Answer: B) CD2, CD3, CD4, CD7, CD8

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16
Q

What is a defining feature of Early T-cell Precursor ALL (ETP-ALL)?
A:
A) CD19 expression
B) Myeloid marker expression
C) Hyperdiploidy
D) Presence of Auer rods

A

Answer: B) Myeloid marker expression

17
Q

What genetic abnormality is rare in adult ALL but common in childhood ALL?

A) t(12;21)
B) t(9;22)
C) NOTCH1 mutation
D) FLT3 mutation

A

Answer: A) t(12;21)

18
Q

What is the function of TdT (Terminal deoxynucleotidyl transferase) in diagnosing ALL?

A) Differentiates B and T cells
B) Identifies mature granulocytes
C) Confirms lymphoid origin
D) Detects plasma cells

A

Answer: C) Confirms lymphoid origin

19
Q

Which feature is more common in AML than ALL?

A) Lymphoblasts
B) Auer rods
C) Mediastinal mass
D) BCR-ABL1 mutation

A

B) Auer rods

20
Q

What symptom is more common in B-ALL than in T-ALL?

A) Mediastinal mass
B) Mucocutaneous bleeding
C) Organomegaly
D) Thrombocytopenia

A

Answer: B) Mucocutaneous bleeding

21
Q

What is the most common morphology of lymphoblasts in ALL?

A) Small lymphoblasts
B) Large lymphoblasts
C) Mixed small and large
D) Auer rod-positive

A

C) Mixed small and large

22
Q

Which ALL subtype is characterized by CD10 positivity?

A) Early B-ALL
B) Intermediate (Common) B-ALL
C) Pre-B-ALL
D) T-ALL

A

Answer: B) Intermediate (Common) B-ALL

23
Q

Which cytogenetic finding is associated with poor prognosis in ALL?

A) Hyperdiploidy
B) t(9;22)
C) t(12;21)
D) Normal karyotype

A

Answer: B) t(9;22)

24
Q

The majority of childhood B-ALL cases show which translocation?
A:
A) t(12;21)
B) t(9;22)
C) t(8;14)
D) t(15;17)

A

A) t(12;21)