25. Leukaemia Flashcards

1
Q

What 4 main pillars are the causes of symptoms of leukaemia?

A

Marrow is replaced
Hyperviscosity
Bone pain
Lymphadenopathy

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2
Q

Give a benign reason for neutrophilia

A

Bacterial sepsis

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3
Q

Give a benign reason for lymphocytosis

A

Viral and immune response

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4
Q

Give a benign reason for eosinophilia

A

Allergy

Parasites

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5
Q

What is acute myeloblastic leukaemia?

A

Malignant transformation of a myeloid precursor

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6
Q

Which groups of people have the most risk of AML?

A

Neonates
Down syndrome
Risk increases with age

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7
Q

How does AML present?

A
Gum hypertrophy
Choroma (skin deposits)
Renal damage
DIC
Hepatosplenomegaly and lymphadenopathy possible but not typical
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8
Q

What causes skin deposits in AML?

A

Tumour lysis syndrome

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9
Q

What causes DIC in AML?

A

Blast cells produce thrombin

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10
Q

Which age group is at risk for acute lymphoblastic leukaemia?

A

Children

Risk decreases with age

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11
Q

How does acute lymphoblastic leukaemia present?

A

Bone pain
Lymphadenopathy
Hepatosplenomegaly
Mediastinal mass and testicular swelling in T cell

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12
Q

What investigations should be done for acute leukaemias?

A

FBC
Bone marrow aspirate and trephine
Immunophenotyping
Molecular analysis

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13
Q

What will be seen on an FBC in acute leukaemia?

A

Very high or very low WBCs and an increase in blasts
Auer rods if AML
Normocytic anaemia
Thrombocytopaenia

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14
Q

How will bone marrow appear in acute leukaemia?

A

Hypercellular

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15
Q

What is immunophenotyping used for?

A

Determine cell type using CD markers

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16
Q

What translocation is associated with AML?

A

t(8;21)

17
Q

What translocation is associated with B-ALL?

A

t(8;14)

18
Q

How are acute leukaemias managed?

A

Chemo +/- bone marrow transplant
Treat infection
Treat bleeding

19
Q

What age group is at risk of chronic myeloid leukaemia?

A

40-60

20
Q

What translocation is associated with CML?

A

Philadelphia chromosome: t(9;22)

21
Q

What are the symptoms of CML?

A

Marrow replacement (fever, anaemia, bleeding)
High WBCs
Hepatosplenomegaly

22
Q

What is the treatment of CML?

A

Hydration to reduce hyperviscosity
Chemo +/- BMT
Imatinib to target BCR-abl gene

23
Q

What age group is at risk of CLL?

A

Elderly

24
Q

What are the symptoms of CLL?

A

Slow development of marrow failure
Lymphocytosis and lymphadenopathy
Hepatosplenomegaly

25
Q

How is CLL treated?

A

Chemo