myeloproliferative neoplasms Flashcards

1
Q

what is a myeloproliferative disorder

A

condition where there is uncontrolled proliferation of a single type of stem cell

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2
Q

what is myelodysplastic syndrome

A

myeloid cells don’t mature properly and produce blasts instead of healthy RBCs
the blasts are immature and can’t carry out the normal functions - normally die in marrow or blood
the blast cells displace the normal bone marrow

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3
Q

what can myelodysplastic syndrome progress into

A

acute myeloid leukaemia

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4
Q

presentation of myelodysplastic syndrome

A

can be asymptomatic
anaemia
frequent/severe infection
purpura, easy bleeding/bruising

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5
Q

investigations for myelodysplastic syndrome

A

FBC - can thrombocytopenia, neutropenia, anaemia
blood film
bone marrow biopsy

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6
Q

risk factors for myelodysplastic syndrome

A

60+

previous chemo/radiotherapy

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7
Q

management of myelodysplastic syndrome

A
supportive 
blood transfusions 
erythropoetic growth factors 
chemo 
stem cell transplant
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8
Q

polycythaemia vera pathology

A

mutation in haematopoetic stem cell causes proliferation of erythroid cell line
increased RBC production
mutated cells become dominant cell type in the marrow

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9
Q

how does polycythaemia vera become myelofibrosis

A

in the ‘spent’ phase of the disease the mutated cells die and are replaced with scar tissue - fibrosis of bone marrow

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10
Q

presentation of polycythaemia vera

A
itch 
increased sweating 
red face and conjunctiva 
iron deficiency anaemia 
hyperviscosity 
stroke 
gout 
splenomegaly
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11
Q

investigations for polycythaemia vera

A

FBC - increased haematocrit, uric acid
serum ferritin
renal and liver function tests
genetic tests for JAK2

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12
Q

treatment of polycythaemia vera

A
venesection 
keep haematocrit below 0.45 in men and 0.43 in women 
aspirin 
hydroxycarbamide 
ruxolitinib
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13
Q

what does the JAK2 mutation do

A

it means the myeloid cells don’t need to be stimulated by erythropoietin to produce RBCs

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14
Q

myelofibrosis pathology

A

fibrosis of bone marrow
RBC production is reduced
liver and spleen start producing RBCs

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15
Q

presentation of myelofibrosis

A

splenomegaly
hepatomegaly
weight loss
fatigue

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16
Q

investigations for myelofibrosis

A

blood film - tear drop cells

bone marrow biopsy

17
Q

management of myelofibrosis

A
transfusion 
hydroxycarbamide 
thalidomide 
JAK2 inhibitors - ruxolitinib 
stem cell transplant
18
Q

essential thrombocytohaemia pathology

A

high platelet count >600
caused by proliferation of megakaryocytic cell line
can progress to AML or myelofibrosis

19
Q

presentation of essential thrombocytohaemia

A
arterial and vanous thrombosis 
digital ischaemia 
gout 
headache 
splenomegaly
20
Q

Investigations for essential thrombocytohaemia

A

FBC - raised platelets

21
Q

management of thrombocytohaemia

A

aspirin
hydroxycarbamide
chemo