Acute Myeloid Leukaemia Flashcards

1
Q

What increases risk of AML?

A

Trisomy 21

Genetics

  • FTL3
  • NPM1
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2
Q

What cell is affected in AML?

A

Myeloid progenitors

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3
Q

Pathology?

A
Mutation in myeloid progenitor - doesn't differentiate
->
accumulation of blasts that can't differentiate
->
Secretion of inhibitory chemokines
->
Inhibition of normal haematopoeisis 
->
Bone marrow failure
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4
Q

Typical presentation?

A

” 58 y/o man presents with tiredness and bruising on his legs. He complains of aching bones and a low grade fever. O/e he has petechiae on his legs. His lymph nodes are non-palpable but he has HSM. “

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5
Q

Symptoms?

A

High cell turnover

Blood cytopenias

  • Thrombocytopenia (petechiae)
  • Neutropenia - repeated infection
  • Infiltrates (gum hypertrophy)
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6
Q

Investigations?

A

FBC

  • Neutropenia
  • Thrombocytopenia

Peripheral film
- Presence of blasts

Bone marrow biopsy

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7
Q

What is present in the blasts in AML?

A

Auer rods

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8
Q

What blasts are found in acute promyelitic leukaemia?

A

Bi-lobed nuclei

Hypergranular

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9
Q

What percentage of bone marrow is filled with myeloid blasts?

A

> 20%

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10
Q

Treatment for AML?

A

Anti-leukaemic chemo

HSCT

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11
Q

What novel monoclonals are there for AML?

A

Gemtuzumab

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12
Q

Treatment for APML?

A

All trans retinoic acid

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13
Q

What drug can be given prophylactically in AML chemo and why?

A

Allopurinol

Increased risk of tumour lysis syndrome

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