Leukaemia Flashcards

1
Q

What is leukaemia?

A
  • neoplastic condition of the bone marrow in which neoplastic cells of lymphoid or non-lymphoid stem cells or their progeny undergo clonal expansion with or without cellular differentiation
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2
Q

Clinical signs due to:

A
  • Failure of normal marrow function
  • Infiltrated organ dysfunction
  • Hyperviscosity of blood (which can increase presence/incidence of thrombosis)
  • Paraneoplastic syndromes (e.g., IMHA, hypercalcaemia)
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3
Q

What tissues may leukaemia cells released into the circulation infiltrate?

A
  • liver
  • spleen
  • LN
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4
Q

ALL

A

= acute lymphoid leukaemia

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5
Q

AML

A

= acute myeloid leukaemia

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6
Q

Which is more responsive to aggressive chemo - ALL or AML?

A
  • ALL
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7
Q

Acute leukaemia - cytology

A
  • can’t tell the difference between lineages (e.g. what this cell type is) as proliferate from stem cells and haven’t matured/differentiated to the point where morphological distinctions can be made
  • very big cells
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8
Q

How does immunophenotyping work to determine the morphology of acute leukaemia?

A
  • lab antibodies against cell surface markers (antigens) tells us origin
  • use immuno-labelled flow cytometry of EDTA blood or marrow
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9
Q

How does lymphocyte clonality PCR work to differentiate acute leukaemia types?

A
  • uses T-cell & B-cell primers to differentiate between B- & T-cell origin
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10
Q

Why is it easy to distinguish the lineage of cells in chronic leukaemia?

A
  • in chronic leukaemia the relevant WBCs look close to normal appearance, there are just WAY to many of them and very large (4x size of small lymphocytes)
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11
Q

Chronic neutrophilic leukaemia - cytology

A
  • majority are mature, segmented neutrophils
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12
Q

How to differentiate a chronic leukaemia from an infection

A
  • numbers high above reference range with continuous increase = neoplastic
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13
Q

What does pancytopenia indicate? (in context of cancer/case suspicious of cancer)

A
  • ablation of normal bone marrow
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14
Q

Once you have diagnosed acute leukaemia, how would you progress?

A
  • send for flow cytology which will detect antigens on surface of cells and enable us to determine if cells are lymphoid or myeloid in origins -> steers tx options
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15
Q

What is lymphoma?

A
  • tumour of the lymphocytes that arises in the LN
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16
Q

What is myelodysplasia?

A
  • a pre-neoplastic condition
  • <20% marrow blasts, cytopaenia and disrupted haematopoiesis
17
Q

What % of leukaemia are aleukaemic?

A
  • ~10%
  • instead there may be atypical cells +/- cytopaenias
18
Q

Acute vs chronic leukaemia

A

Acute:
- neoplastic transformation during stem cell proliferation
- aggressive rapid disease
- cytopaenia very common (marrow disrupted by neoplastic expansion)

Chronic:
- neoplastic transformation following differentiation
- slow progression and less aggressive cf aute
- cytopaenia is rare

19
Q

When there is marrow disruption, which cells disappear first? then what?

A
  • neutrophils (hours)
  • platelets (days)
  • RBCs (months)
20
Q

Lymphoma with a leukaemia phase

A
  • In severe cases: stage V lymphoma
  • goes to bone marrow -> infiltrates the bone marrow and then get them circulating
21
Q

Lymphoma vs lymphoid leukaemia

A

Lymphoma involving BM:
- <25% blast cells in marrow
- Lower circulating blast count
- Mild or absent cytopenia
- Massive lymphadenopathy
- May not be systemically ill

ALL:
- >25% blast cells in marrow
- Higher circulating blast count
- Severe cytopenia
- Mild to moderate lymphadenopathy
- Usually systemically ill