Acute Leukaemia Flashcards

1
Q

What is acute leukaemia?

A

The accumulation of early MYELOID or LYMPHOID precursors in the BONE MARROW and other tissues

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2
Q

What is leukaemia usually the result of?

A

Mutations in haemopoietic stems cells

  • Cannot differentiate into mature blood cells
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3
Q

What are the two main types of leukaemia?

A

Lymphoid leukaemia

Myeloid leukaemia

(further divided into various subgroups)

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4
Q

What are the features of blast cells in AML?

A
  • High nucleus:cytoplasm ratio

- presence of granule

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5
Q

What are the feature of blast cells in ALL?

A

Higer nucleus:cytoplasm ration (very little cytoplasm)

  • smaller than AML blasts
  • rounder
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6
Q

What are the clinical features of acute leukaemia? What are the specific

A

Anaemia - hypochromic, microcytic

Infection (immunocompromised e.g. candida, perianal infection - E coli, strep faecalis)

Early bruising/haemorrhage - thrombocytopenia

Organ infiltration by leukaemia cells e.g. spleen, liver, meninges, testes, skin

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7
Q

How is acute leukaemia diagnosed?

A

Morphology - look at cells!

Immunological markers**

Cytogenetics

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8
Q

How are acute myeloid leukaemia classified? What are the two classification systems and what do they look at?

A

French American and British (FAB) - morphological features - see different points in maturation

WHO - risk adapted

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9
Q

How does immunological markers work?

A

Monoclonal antibodies with fluorochrome attached added

Attached to cell surface antigens

Fluorochrome absorbs light and releases wavelength

  • Indicates presence of antigens which = diagnostic
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10
Q

What is trisomy 9:22? (T(9;22))

A

Philadelphia chromosome - driver for chronic myeloid leukaemia

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11
Q

What cytogenetic abnormalities are associated with a good and bad prognosis of Acute leukaemia?

A

T(15:17) (T8:21) = good prognosis

Mysomy -5, -7 = bad

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12
Q

What type of chromosomal abnormalities are associated with ALL?

A

Abnormalities in number of chromosomes

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13
Q

What are the poor prognostic factors for ALL?

A
  • Increasing age (>10yrs)
  • High white cell count (>50)
  • Male
  • Cytogenetic abnormalities (discussed)
  • T cell - ALL (worse than B-cell ALL)
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14
Q

What genetic mutations are associated with a good and poor diagnosis?

A

NPM1 = good

FLT3 - bad

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15
Q

What is the management for AML?

A

Chemotherapy - 4 courses - 2 intensive, 2 consolidation (obtain remission)

Bone marrow transplant in young patient

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16
Q

What is the management for ALL?

A

Induction and intensive consolidation chemotherapy

Prophylaxis of meningeal leukaemia with methotrexate

Bone marrow transplant in bad risk patients

17
Q

What is neutropenic sepsis? How is it diagnoses>

A

Intensive chemotherapy will destroy patient neutrophils

Pyrexia with neutrophil count being less than 1 x19^9

18
Q

How is neutropenic sepsis managed?

A

Rapid administration of broad spectrum IV antibiotics

Protective isolation

Prophylactic antibiotics

Use of GCSF