Acute Leukaemia Flashcards

1
Q

Define leukaemia.

A

Any of a group of malignant diseases in which the bone marrow and other blood-forming organs produce increased numbers of abnormal white blood cells

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2
Q

What is the cut off between myelodysplastic syndromes and acute leukaemia?

A

20% blast cells in the bone marrow

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3
Q

What are the 4 types of acute leukaemia?

Which cells do they affect?

A

Stem cell leukaemia (haemopoietic stem cells)
Acute myeloid leukaemia (RBCs, neutrophils, monocytes etc.)
Acute lymphoid leukaemia (B cells, T cells)
Biphenotypic leukaemia (all cells)

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4
Q

Which type of acute leukaemia is more common in childhood?

Which type of leukaemia is more common in elderly age?

A

Childhood - ALL

Elderly - AML

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5
Q

List 7 causes of acute leukaemia.

A
Idiopathic
Chemicals
Chemotherapy
Radiotherapy
Genetics (e.g. Fanconi syndrome)
Pre-leukaemias
Viruses
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6
Q

Describe the symptoms of acute myeloid leukaemia. (8)

A
Rapid onset
Lethargy
Increased susceptibility to infection
Bleeding and easy bruising
Bone pain
Gum swelling
Lymphadenopathy
Skin rash
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7
Q

Describe the features of a peripheral blood film in acute myeloid leukaemia. (4)

A

Anaemia
Neutropenia
Thrombocytopenia
Blast cells

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8
Q

Describe the features of blast cells on a blood film. (2)

A

Large

High nuclear:cytoplasm ratio

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9
Q

Describe the features of the bone marrow in acute myeloid leukaemia. (1)

A

20% blast cells

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10
Q

Which mutations indicate a good prognosis in AML? (3)

A

T(15:17)
Inv16
T(8:21)

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11
Q

How do you differentiate between AML and ALL?

Describe how this test works.

A

Flow cytometry

  1. Sample cells passed through a narrow channel, one at a time
  2. Light illuminates the cells (some may also be stained with fluorescence)
  3. Sensors detect the types of light refracted from each cell; each cell type will have a different pattern
  4. Data collected to determine which cell types there are more of
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12
Q

List 6 poor prognostic factors in AML.

A
Secondary AML
Relapsed AML
Progression of MDS to AML
Biphenotypic disease
Elderly patients
Refractory AML
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13
Q

How would you treat AML? (3)

A
Intensive chemotherapy (for young, otherwise fit patients)
Low dose chemotherapy (for old, frail patients)
Supportive care only (for patients too frail for chemo)
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14
Q

How is intensive chemotherapy used in treating AML? (3)

A

Patients entered onto clinical trials to achieve optimal therapy

Types of chemo: antracycline, cytarabine

Cure rate: 15-90%

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15
Q

Define remission of AML.

How common is relapse in AML?

A

<5% blast cells

Relapse in 40-50%

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16
Q

Describe how you would monitor patients after chemotherapy.

A

Every 6-8 weeks for 1st year after treatment

Look for psychological issues

17
Q

Describe the clinical features of acute lymphoid leukaemia. (3)

A

Limping
Purpuric rash
Bone pain

18
Q

What investigations would you do to diagnose ALL? (3)

A
Bone marrow aspirate (10+% blast cells)
Flow cytometry 
Cytogenetics, e.g.
-FISH
-Karyotyping
-Reverse transcriptase PCR (detects fusion genes)
19
Q

List 2 genetic abnormalities involved in ALL.

A

T(9:22)

T(4:11)

20
Q

How would you manage ALL? (8)

A

Intensive chemotherapy
-CNS directed

Supportive treatment:

  • Blood transfusion
  • Fresh frozen plasma
  • Platelet transfusion
  • Antibiotics
  • Growth factors (e.g. G-CSF)
  • Granuloyctes

Allogenic stem cell transplant

21
Q

List 4 indications for stem cell transplant in ALL.

A

Relapse
Refractory ALL
Poor prognosis
Age <60 yo)