Acute Leukaemia Flashcards

1
Q

what is acute leukaemia

A

haematopoietic blast cells constitute >20% bone marrow cells

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2
Q

what is the most common type of malignancy in childhood

A

ALL

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3
Q

when does AML occur

A

at all ages

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4
Q

clinical features

A

short hx symptoms due to bone marrow failure- anaemia, abnormal bruising/bleeding, infection; weating, fever, weight loss, malaise

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5
Q

what signs are present

A

lymphadenopathy and hepatosplenomegaly freq especially in ALL

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6
Q

what is common in promyelocytic AML

A

DIC

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7
Q

lab features

A

anaemia, thrombocytopenia, neutropenia. leucocytosis. infiltration by blast cells.

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8
Q

good prognostic features in ALL

A

female, 2-9 years, low WCC, absent extramedullary disease, 4 weeks remission speed, 1 week clearance peripheral blood blasts, negative minimal residual disease in bone marrow at 1-3m

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9
Q

good prognostic indicators in AML

A

remission after one course chemo.

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10
Q

what can AML be a result of (iatrogenic)

A

chemo treatment eg for lymphoma

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11
Q

what is AML associated with

A

myelodysplastic states, radiation, syndromes. progresses rapidly

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12
Q

what rods are diagnostic of AML

A

auer rods

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13
Q

what is the first stage of treatment

A

remission induction- high dose intensive combination chemo - reduce or eradicate leukaemic cells from bone marrow, re establish normal haemopoiesis. post induction chemo- initially intensive then for ALL less- maintenance chemo

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14
Q

what is remission

A

normal FBC,

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15
Q

treatment AML

A

anthracycline- daunorubicin, cytosine arabinoside.

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16
Q

prognosis AML

A

80% 85% with 2 courses. 30-50% cured 15-55yrs

17
Q

treatment ALL

A

remission induction with vincristine, dexamethasone and L-asparaginase; often with daunorubicin or cyclophosphamide.

18
Q

what is maintenance and how long for in AML

A

mercaptopurine daily, weekly methotrexate, monthly vincristine and dexamethasone. for further 2-3 years

19
Q

what system is commonly involved in ALL

A

CNS- so give intrathecal methotrexate and high dose systemic chemo

20
Q

when can stem cell transplant be used

A

allogeneic stem cell transplantation in adults

21
Q

prognosis ALL

A

80% children cured

22
Q

what is tumour lysis syndrome

A

metabolic abnormalities due to the massive destruction of cells. hyperkalaemia, incr urate, decr calcium, renal injury

23
Q

treatment tumour lysis syndrome

A

fluid intake and allopurinol

24
Q

side effects cancer treatment

A

tumour lysis syndrome, hyperviscosity, DIC, neutropenic sepsis

25
Q

what happens in hyperviscosity

A

if WCC >100x10^9/l thrombi in brain, lungs, heart.

26
Q

treat hyperviscosity

A

lower WCC with hydroxycarbamide, transfusion

27
Q

what is neutropenic sepsis

A

neutrophils

28
Q

treatment neutropenic sepsis

A

piperacillin-tazobactam (tazocin)

29
Q

what treatment can you give in promyelocytic leukaemia

A

trans retinoic acid