Pediatric Leukemia Flashcards

1
Q

Most common malignant neoplasms in childhood?

A

Leukemia

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2
Q

What causes increased incidence in ALL in kids?

A

Medical radiation

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3
Q

Most common genetic cause of leukemias?

A

Translocations

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4
Q

Most common and easily curable form of childhood leukemia?

A

ALL Acute Lymphoblastic Leukemia

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5
Q

ALL affects lymphocytes, but which lymphocyte line is the most commonly affected?

A

B-cell lineage

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6
Q

What occurs in ALL?

A

BM produces immature cells that develop into leukemic lymphoblasts that build up and crowd out the healthy cells

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7
Q

Who is most likely to get ALL?

A

White males between 2-5 years of age

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8
Q

What adds an increased risk of getting ALL?

A

Kids with chromosomal abnormalities

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9
Q

What happens with ALL in twins?

A

Risk is greater than 70% of second twin getting ALL if first twin was diagnosed during first year of life and they shared a placenta
If first develops ALL by 5-7 then risk of second twin is 2x risk of getting than general population

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10
Q

Most important distinguishing morphologic feature of a ALL subtype?

A

FAB L3 subtype-evidence of a mature B-cell leukemia AKA Burkitt Leukemia

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11
Q

What feature of ALL is adequate to establish an ALL diagnosis?

A

Morphology

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12
Q

Two chromosomal abnormalities most seen in ALL:

A

12 -> 21 favorable prognosis (more common)

9 -> 22 poor prognosis

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13
Q

Clinical manifestation of ALL infiltrating leukemic cells into normal tissues resulting in BM failure?

A

Anemia
Neutropenia
Thrombocytopenia

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14
Q

What site does B-ALL usually manifest and create significant problems?

A

Testes

CNS

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15
Q

Where does T-ALL usually manifest and create significant problems?

A

Anterior mediastinal mass (thymic mass)

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16
Q

How is ALL diagnosis confirmed?

A

Immature blast cells on peripheral blood smear or BM biopsy

17
Q

What important test is done at the time of ALL diagnosis?

A

Lumbar puncture

18
Q

ALL prognosis four groups and criteria?

A

Low risk
Standard risk
High risk
Very high risk

19
Q

Low risk criteria:

A

1-9 years old; initial WBC less than 50k; 12->21

20
Q

High risk criteria:

A

Younger than 1 year old or 10 years old and older; initial WBC greater than 50k; CNS or Testicular disease; 4->11

21
Q

Very high risk criteria:

A

Missing 1 or more chromosomes; 9->22; or fail to achieve remission after 4 weeks of therapy

22
Q

What are the markers on T-ALL cells?

A

TdT+

23
Q

What are the markers on B-ALL cells?

A

CD10+

24
Q

What percent of childhood leukemias are AML?

A

11%

25
Q

Most common classification system for AML subtypes?

A

FAB system

26
Q

What percent of childhood leukemias are CML?

A

2-3%

27
Q

What gene causes CML?

A

9->22 translocation