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?

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
what cell is increased in Essential Thrombocythaemia?
increase of platelets
26
state some symptoms of Essential Thrombocythaemia?
arterial and venous thromboses digital ischaemia gout
27
what occurs in idiopathic myelofibrosis ?
fibrosis in bone marrow due to megakaryocytes | - It makes fewer red blood cells and usually too many white blood cells.
28
can leukaemic cells differentiate in acute or chronic myeloid leukaemia ?
can differentiate in chronic myeloid leukaemia
29
what is the prognosis of chronic myeloid leukaemia ?
survival is a few years and is incurable without bone marrow transplantation
30
what are the two main types of acute myeloid leukaemia ?
Acute Myeloblastic Leukaemia (AML) Acute Lymphoblastic Leukaemia (ALL)