Acute lymphoblastic leukaemia Flashcards

1
Q

What cells are affected?

A

lymphoid progenitor cells become genetically altered -> uncontrolled proloiferation
early lymphoid precursors replace normal haematopoietic cells of BM + tissue infiltration

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2
Q

What age group is mostly affected?

A

children 75% occur in under 6 yrs

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3
Q

What are the signs and sx?

A
  1. BM failure - anaemia, infection, bleeding
  2. Infiltration - lymphadenopathy (painless and mobile), hepatosplenomegaly, CNS involvement
  3. Fever
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4
Q

What features suggest CNS involvement?

A

Meningism, papilloedema, cranial nerve palsies

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5
Q

Where do infections commonly occur ?

A
bacterial septicaemia
zoster
CMV
measles 
candidiasis
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6
Q

What investigations would you do?

A
  1. FBC - normocytic, normochromic anaemia w low reticulocyte count, leukocytosis
  2. Peripheral blood smear
  3. U&ES, LFTs
  4. BM biopsy
  5. CXR, CT scan
  6. LP - look for CNS involvement
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7
Q

What supportive treatment twould you give?

A
  1. Blood/platelet transfusion
  2. IV fluids
  3. allopurinol to prevent tumour lysis syndrome
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8
Q

How would you treat neutropenia/

A

Prophylactic:

  • abx
  • antivirals
  • antifungals
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9
Q

What regimen of chemotherapy would you give?

A
  1. Remission induction
  2. Consolidation
  3. CNS prophylaxis
  4. Maintenance
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10
Q

What drugs would you give to induce remission?

A

Vincristine
Pred
L-asparaginase
Daunorubicin

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11
Q

What drugs would u give for CNS prophylaxis

A

intrathecal methotrexate +/- CNS irradiation

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12
Q

What drugs would u give to maintain remission?

A
Prolonged chemo:
mercaptopurine
methotrexate
vincristine 
pred
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13
Q

What treatment aims to give complete remission

A

Matched related allogeneic marrow transplantations

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14
Q

What are the 3 ways in which ALL can be classified?

A
  1. Morphologically
  2. Immunologically - precursor B cell (75%), T-cell, B cell
  3. Cytogenetically - chromosomal analysis
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15
Q

What is used to detect residual disease?E

A

PCR

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