acute leukemia Flashcards

(31 cards)

1
Q

generally speaking what is a leukemia ?

A

cancer of white blood cells, the cells appear in the peripheral blood

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2
Q

what is the main difference between acute and chronic leukemias ?

A

acute - associated with blast cells
chronic - associated with no blast cells

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3
Q

what age group is highly associated with ALL ?

A

children and adolescent

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4
Q

what is an important differential diagnosis of ALL in children ?

A

pertussis

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5
Q

how can we differentiate between pertussis and ALL ?

A

pertussis comes with symptoms of hypoglycemia and is associated with post tussive emesis , which is not present in ALL

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6
Q

what are the positive immune markers associated with ALL ?

A

TdT and CD10
“ happens in Ten year olds”

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7
Q

what genetic disease is associated with a higher risk of ALL?

A

down syndrome - where there is a higher risk of excess lymphoblasts

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8
Q

what are the gene translocations associated with ALL and what are their prognosis ?

A

associated with 9;22 - Philadelphia chromosome - worse prognosis

12;21 - better prognosis

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9
Q

what are TdT and CD10 markers of ?

A

TdT markers of pre t and pre b cells
CD10 are markers for pre B cell

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10
Q

what are the most common sites of metastasis associated with ALL ?

A

CNS and testes

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11
Q

what is seen on peripheral blood smear in ALL ?

A

lymphoblasts

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12
Q

what are the markers for mature B cells ?

A

Cd19, CD20, CD21

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13
Q

if you see positive TdT what does this indicate ?

A

lymphocyte lineage not seen in myeloblasts

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14
Q

what are the antigens associated with T cells ?

A

CD 1 all the way to CD 8

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15
Q

what is the usual lineage of ALL ?

A

usually a pre B cell malignancy

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16
Q

what is the presentation associated with T cell ALL ?

A

presents similarly to SVC syndrome
presents as a mediastinal mass , with a positive pemberton sign and congested neck veins

17
Q

what are the markers seen in T cell ALL ?

18
Q

what is the most common age group associated with AML ?

A

65 year olds is the median age

19
Q

what is the mechanism associated with AML ?

A

symptoms are due to bone marrow suppression

20
Q

what are the pripheral blood smear findings associated with AML ?

A

auer rods seen
or 30-50% blasts seen
myeloperoxidase positive

21
Q

how can we differentiate between AML and ALL ?

A

ALL is MPO negative whist AML is MPO positive
also ALL happens in younger patients
if you see lymphoblasts thats definetly ALL and not AML

22
Q

what is the gene translocation associated with AML ?

A

a common subtype of AML is APL associated with 15;17 (PML RARA)
the retinoic acid receptor is on chromosome 17

23
Q

what complication is associated with the release of Auer rods in the circulation ?

A

associated with the onset of DIC

24
Q

what is the treatmet for AML

A

the APL subtyppe is treated with all trans retinoic acid which allows the maturation of leukemic cells into granulocytes (mature)

25
what does a mutation in RAR lead to ?
prevents the maturation of promyelocytes
26
what is the leukocytes LAP score ?
helps differentiate if the leukocyte reaction is due to infection or malignancy if the score is high it is a leukomoid reaction if it is low then this is CML
27
what is the myelodysplastic syndromes ?
like a minor version of AML where there is abnormal myeloid progenitor cells , leading to ineffective hematopoesis
28
what is seen on biopsy of the BM in MDS ?
hypercellular BM with dysplasia
29
what is the prognosis of MDS ?
may progress to AML
30
what is the difference in terms of the number of blasts in MDS vs in AML ?
MDS has a low blast count AML has a high blast count
31
what is seen on peripheral blood smear in MDS ?
pseudo - pelger huet anomaly , where there are neutrophils with bilobed duet nuclei