6.2 Acute Leukemia Flashcards

1
Q

What is the basis for acute leukemia?

A

Accumulation of blast cells d/t cell inability to mature properly

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2
Q

Acute leukemia is defined as what?

A

When there is >20% of blasts in the bone marrow

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3
Q

What is the cause of the ssx of acute leukemia?

A

blast cells crowding out normal cells/not producing normal cells (so anemia, neutropenia, leukopenia etc)

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4
Q

Why is there a high WBC count if there are not any mature cells being produced in leukemia?

A

Tons of blasts

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5
Q

What are the histological findings of acute leukemia?

A

Large, immature cells with punched out nucleoli

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6
Q

What is the marker for ALL? AML?

A
ALL = tdt
AML= myeloperoxidase
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7
Q

tdt in the nucleus of an immature WBC = what disease? What is tdt?

A

ALL

DNApol in lymphoblasts

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8
Q

Auer rod = what disease?

A

AML

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9
Q

Down syndrome is associated with what hematological malignancy? What age does this appear after?

A

ALL

After age of 5 yo

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10
Q

Who usually gets ALL?

A

Children

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11
Q

What are the two division of ALL?

A

B-ALL

T-ALL

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12
Q

B-ALL surface markers = ?

A

CD10
CD19
CD20

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13
Q

What is the prognosis for B-ALL?

A

Good with chemo

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14
Q

What parts of the body need to be given prophylaxis of chemo for B-ALL?

A

scrotum and CSF

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15
Q

What are the two translocations associated with B-ALL? Which is associated with children and has a good prognosis, and which with adults and has a bad prognosis?

A
t(12;21) = kids
t(9;22) = adults (philadelphia chromosome)
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16
Q

What are the cell markers for T-ALL?

A

CD2 thru CD8

17
Q

What are the signs of T-ALL that distinguish it from B-ALL?

A

Thymic mass in a teenager

18
Q

Diseases whose names end in -oma are what?

A

Masses

19
Q

What are auer rods?

A

Crystallized myeloperoxidase–an enzyme only found in myeloblasts, hence why these are pathognomonic for AML

20
Q

Punched out nucleolus = ?

A

Lymphoblasts

21
Q

Who gets AML?

A

Old people (50-60)

22
Q

What are the three types of classification in AML?

A
  • Cytogenetic abnormalities
  • Lineage of myeloblasts
  • Surface markers
23
Q

What is the chromosomal translocation found in acute promyelocytic leukemia?

A

t(15;17)

24
Q

What disease is caused by a t(15;17)? how?

A

Acute promyelocytic leukemia

Retinoic acid receptor disrupted, inhibiting promyelocyte maturation

25
Q

Promyelocytes that contain numerous Auer rods, as seen in acute promyelocytic leukemia, poses a risk for what complication?

A

DIC

26
Q

What is the treatment for acute promyelocytic leukemia?

A

ATRA (all trans-retinoic acid)–very good prognosis

27
Q

What is the cause of acute monocytic leukemia? What is the telltale sign of this?

A

Proliferation of monoblasts that lack MPO

Infiltration of the gums = gingival hypertrophy

28
Q

What is the cause of acute megakaryoblastic leukemia? What disease is associated with this?

A

Proliferation of megakaryocytes that lack MPO

Down syndrome BEFORE age 5)

29
Q

What is the CA that appears before the age of 5 for down syndrome pts? After?

A
Before = acute megakaryoblastic leukemia
After = ALL
30
Q

What chemotherapeutic agent can lead to AML?

A

Alkylating agents

31
Q

What condition may cause an increased risk of developing AML?

A

Preexisting dysplasia

32
Q

What is myelodysplastic syndrome?

A

Cytopenia with hypercellular bone marrow

33
Q

Abnormal maturation of myeloid progenitor cells with 20%?

A

20% acute myeloid leukemia