Leukaemia Flashcards

(43 cards)

1
Q

Leukaemia

A

cancer of a particular line of stem cells in the bone marrow

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2
Q

4 types

A

AML
CML
ALL
AML

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3
Q

pancytopenia

A

low platelets
low RBC
low WBC

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4
Q

most common leukaemia in children under 5

A

ALL

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5
Q

typical features

A
fatigue
fever
failure to thrive
pallor 
petechiae/abnormal bruising
LN
hepatosplenomegaly
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6
Q

petchiae differentials

A
leukaemia
meningococcal septicaemia
vasculitis 
NAI
ITP
HSP
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7
Q

diagnosis

A
FBC
blood film 
lactate dehydrogenase
bone marrow biopsy
LN biopsy 
CXR, lumbar puncture, CT/MRI/PET
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8
Q

blood film

A

abnormal cells and inclusions

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9
Q

definitive diagnosis

A

bone marrow biopsy

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10
Q

bone marrow aspirate

A

liquid sample full of cells from bone marrow

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11
Q

bone marrow trephine

A

solid core sample of bone marrow and better assessment of cells and structure

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12
Q

where is bone marrow biopsy usually taken from?

A

iliac crest

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13
Q

what happens in ALL?

A

malignant change in lymphocyte precursor cells

acute proliferation of (usually) B lymphocytes

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14
Q

why is there pancytopenia in ALL?

A

B lymphocytes take over bone marrow and replace other cells

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15
Q

what is ALL often associated with?

A

downs syndrome

ionising radiation in pregnancy

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16
Q

ALL blood film

A

blast cells

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17
Q

ALL genetic association

A

philadelphia chromosome 30% adults but only 5% children

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18
Q

who is usually affected by CLL?

A

adults over 55

19
Q

CLL symptoms

A

often asymptomatic

infections, anaemia, bleeding and weight loss

20
Q

what can CLL cause?

A

warm autoimmune haemolytic anaemia

21
Q

what can CLL transform into?

A

high grade lymphoma

richter’s transformation

22
Q

blood film CLL

A

smear or smudge cells

23
Q

3 phases of CML

A

chronic phase
accelerated phase
blast phase - crisis

24
Q

how are those with CML often diagnosed?

A

asymptomatic raised WCC

25
characteristic cytogenic change CML
philadelphia chromosome
26
philadelphia chromosome
chr 9 and 22 translocation | CML
27
treating CML - what drug has revolutionalised treatment?
imatinib | BCR-ABL tyrosine kinase inhibitor
28
most common acute leukaemia in adults
ALL
29
what can ALL progress from?
myeloproliferative disorder polycythaemia ruby vera myelofibrosis
30
blood film AML
blast cells | auer rods in cytoplasm
31
how long is asymptomatic phase of CML?
5 years
32
complications of chemotherapy
``` failure stunted growth in children infections infertility tumour lysis syndrome neuro/cardiotoxicity ```
33
what causes tumour lysis syndrome?
release of uric acid from cells destroyed by chemo
34
impact of uric acid in TLS
crystals in interstitial tissue and tubules in kidney - AKI
35
treating tumour lysis syndrome
allopurinol or rasburicase potassium and phosphate monitoring calcium monitoring
36
Is CNS involvement common in ALL?
yes
37
3 classifications of ALL
morphological - FAB cytogenic - philadelphia immunological
38
ALL treatment
remission consolidation CNS prophylaxis maintenance
39
ALL cure rate children
70-90%
40
only cure for CML
stem cell transplant -HLA matched
41
treating CLL
fludarabine rituximab cyclophosphamide
42
staging for CLL
binet staging | rai stage
43
binet staging
``` A = fewer 3 LN B = >3 LN C = anaemia and low platelets ```