Myeloid Malignancy Flashcards

1
Q

state the four main types of myeloid malignancies?

A

chronic myeloid leukaemia
acute myeloid leukaemia
Myelodysplastic Syndromes (MDS)
Myeloproliferative Diseases (MPD)

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2
Q

does chronic or acute myeloid leukaemia use bone marrow failure?

A

acute myeloid leukaemia

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3
Q

what gene is responsible for the translocation mutation of t(9;22)

A

gene BCR-ABL

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4
Q

what medication stops the gene BCR-ABL from working?

A

tyrosine kinase inhibitor

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5
Q

does bone marrow failure occur in chronic myeloid leukaemia ?

A

no

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6
Q

what are some symptoms of chronic myeloid leukaemia ?

A
anaemia 
splenomegaly 
weight loss 
gout 
hyperleukostasis
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7
Q

what is hyperleukostasis?

A

total leukemia blood cell count greater than 50 x 109/L

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8
Q

what do the blood results show in AML?

A

high WCC/platelets
anaemia
bone marrow is hyper cellular

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9
Q

what is the treatment of CML?

A

tyrosine kinase inhibitors

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10
Q

what is a cure for AML?

A

bone marrow transplantation

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11
Q

state the features of bone marrow failure?

A

anaemia
thrombocytopenia
infection due to neutropenia

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12
Q

what is the treatment for AML?

A

supportive care
anti-leukaemic chemo
stem cell transplantation
targeted antibodies

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13
Q

what investigations should be done for AML?

A

blood count and blood film
bone marrow aspirate
cytogenetics of leukaemic blasts
molecular genetics for associated acquired gene mutations

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14
Q

state some associated been mutations with AML?

A

FLT3
NPM1
IDH 1 and 2

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15
Q

what age is myelodysplastic syndromes common in?

A

old age

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16
Q

what are the two symptoms of myelodysplastic syndromes?

A

macrocytic anaemia

pancytopenia

17
Q

what is the treatment for myelodyaplastic syndromes?

A

supportive

stem cell transplantation

18
Q

does acute or chronic myeloid leukaemia have high or low platelet count?

A
acute = low 
high = high
19
Q

what are the three types of myeloproliferative disorders?

A

polycythaemia vera
essential thrombocythaemia
idiopathic myelofibrosis

20
Q

state the mutation that causes polycythaemia vera?

A

JAK2

21
Q

what does the JAK2 mutation lead to

A

increased phosphorylation

22
Q

what happens to cell counts in polycythaemia vera?

A

increased haemoglobin, haematocritt, platelets, WCC and megakaryocytes
raised uric acid
increased neutrophils and lymphocytes

23
Q

state some symptoms of polycythaemia vera?

A
headaches 
itch 
thrombosis 
TIA/stroke 
splenomegaly
24
Q

what is the treatment for polycythaemia vera?

A

venesection - removal of blood, since plasma is produced faster than RBCs
aspirin
inhibitor of JAK2

25
Q

what cell is increased in Essential Thrombocythaemia?

A

increase of platelets

26
Q

state some symptoms of Essential Thrombocythaemia?

A

arterial and venous thromboses
digital ischaemia
gout

27
Q

what occurs in idiopathic myelofibrosis ?

A

fibrosis in bone marrow due to megakaryocytes

- It makes fewer red blood cells and usually too many white blood cells.

28
Q

can leukaemic cells differentiate in acute or chronic myeloid leukaemia ?

A

can differentiate in chronic myeloid leukaemia

29
Q

what is the prognosis of chronic myeloid leukaemia ?

A

survival is a few years and is incurable without bone marrow transplantation

30
Q

what are the two main types of acute myeloid leukaemia ?

A

Acute Myeloblastic Leukaemia (AML)

Acute Lymphoblastic Leukaemia (ALL)