Myeloproliferative Neoplasms Flashcards

(40 cards)

1
Q

acute myeloid leukemia

A

myelodysplastic syndromes

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2
Q

acute myeloid leukemia

A

myelodysplastic syndromes

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3
Q

acute lymphoid leukemia

A

lymphoma

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4
Q

chronic myeloid leukemia

A

myeloproliferative neoplasms

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5
Q

chronic lymphoid leukemia

A

lymphoma

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6
Q

characteristics of acute

A

kids

cells can’t mature

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7
Q

characteristics of chronic

A

adults

cells can’t die

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8
Q

age for myeloproliferative neoplasms

A

40-60y

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9
Q

marrow cellularity

A

increased

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10
Q

barrow blasts

A

normal to increased

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11
Q

mature or immature cells

A

mature

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12
Q

morphology

A

normal

abnormal megakaryocytes

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13
Q

hematopoesis

A

effectiveness

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14
Q

cell lines increased

A

1 or more
RBC
granulocytes
megakaryocytes

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15
Q

organ enlargment

A

common
liver
spleen

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16
Q

signaling pathway involved

A

tyrosine kinase

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17
Q

chronic pahse

18
Q

acute blast phase

A

> 20% blasts

marrow failure

19
Q

acute blast phase

A

> 20% blasts

marrow failure

20
Q

polycythemia vera

A
increased proliferation of erythroid precursors
JAK2 mutation
male
issues due to high viscosity blood
poikilocytosis
treatment- phelobotmy
decreased EPO
increased RBC mass in proliferative phase only
spent phase- normal/decreased RBC mass
21
Q

chronic myeloid leukemia

A

myeloproliferative neoplasms

22
Q

chronic lymphoid leukemia

23
Q

characteristics of acute

A

kids

cells can’t mature

24
Q

characteristics of chronic

A

adults

cells can’t die

25
age for myeloproliferative neoplasms
40-60y
26
marrow cellularity
increased
27
barrow blasts
normal to increased
28
mature or immature cells
mature
29
morphology
normal | abnormal megakaryocytes
30
hematopoesis
effectiveness
31
cell lines increased
1 or more RBC granulocytes megakaryocytes
32
organ enlargment
common liver spleen
33
signaling pathway involved
tyrosine kinase
34
chronic pahse
35
accelerated phase
10-19% blasts
36
acute blast phase
>20% blasts | marrow failure
37
chronic myelogenous leukemia
increased proliferation of granulocytes, specifically basophils 9,22 translocation- BCR/ABL fusion protein (philadelphia chromosome) splenomegaly treatment- imatinab LAP negative
38
polycythemia vera
``` increased proliferation of erythroid precursors JAK2 mutation male issues due to high viscosity blood treatment- phelobotmy decreased EPO increased RBC mass in proliferative phase only spent phase- normal/decreased RBC mass ```
39
essential thrombocytopenia
``` increased platelets JAK2 mutation 30y female avoid splenectomy doesn't progress to marrow fibrosis or acute leukemia ```
40
primary myelofibrosis
``` increased megakaryocytic JAK2 mutation splenomegaly- extra medullary hematopoiesis poikilocytosis marrow fibrosis leukoerythroblastic smear ```