Acute Leukemias Flashcards

1
Q

How does leukemia arise?

A

Clonal proliferation of a single hematopoietic stem cell in the bone marrow, preventing normal blood cell production

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2
Q

What is diagnostic of acute leukemia on bone marrow aspirate/biopsy?

A

> 20% blasts in bone marrow

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3
Q

What are the signs/symptoms of bone marrow failure?

A

Bony pain, pancytopenia

Pallor, breathlessness, fatigue
Increased infections
Bruising, bleeding

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4
Q

What is the age group of patients affected by AML?

A

Older adults

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5
Q

What is the age group of patients affected by ALL?

A

Children

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6
Q

What is the prognosis of AML?

A

Poor

Median survival 12-24 months

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7
Q

What is the prognosis of ALL?

A

Good

80% longterm remission in childhood ALL

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8
Q

Where does AML tend to infiltrate?

A

Gingiva

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9
Q

Where does ALL tend to infiltrate?

A
Lymph nodes (lymphadenopathy)
CNS (meningeal signs), uncharacteristic of AML
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10
Q

What is seen on peripheral blood film for AML?

A

Auer Rods, granules

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11
Q

What is seen on peripheral blood film for ALL?

A

No granules.

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12
Q

Which acute leukemia is leukostasis characteristic of?

A

AML

“sticky” blasts sludge the microvasculature, leading to hypoxia and hemorrhage

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13
Q

What is special about acute promyelotic leukemia?

A

Subset of AML
No chemo
ATRA to induce differentiation

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14
Q

How is AML treated?

A

Induction chemo for complete remission (no peripheral blasts, <5% blasts in BM)

Consolidation chemo to prevent recurrence

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15
Q

How is ALL treated?

A

Induction chemo to induce complete remission

Consolidation to prevent recurrence

Maintenance chemo (low dose over long period)

Prophylactic CNS radiation or MTX

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