120214 cases Flashcards

1
Q

toxic change

A

indicates presence of primary granules
in neutrophils
for severe inflam

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2
Q

how is CML diagnosed?

A

Philadelphia chromosome (but also get a biopsy)

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3
Q

etiology of CML?

A

irradiation in 5%

unknown in rest

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4
Q

what can CML progress to?

A

acute leukemia

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5
Q

hepatic vein thrombosis/venous thrombosis

A

think polycythemia vera (increased RBC mass leading to viscosity)

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6
Q

DIC

A

think APL (type of AML)

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7
Q

myelodysplastic syndrome–wbc count?

A

low

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8
Q

t(15;17) is associated with

A

APL (type of AML)

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9
Q

APL is a medical emergency-why?

A

can have DIC

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10
Q

hypogranular and hypolobated neutrophil
large hypogranular platelet
giant platelet

A

MDS

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11
Q

what differentiates MDS from AML with MDS-associated changes?

A

the bone marrow blast percentage

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12
Q

WHO classification of AML

A

AML with recurrent cytogenetic abnormalities
AML with MDS-associated changes
AML and MDS, therapy related
AML not otherwise categorized

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13
Q

therapies for MDS

A

stem cell transplantation or supportive care
or
hypomethylating agents (to allow cell to divide)

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14
Q

decitabine

A

hypomethylating agent

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15
Q

increased blasts going into blood will result in

A

increased WBC count

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16
Q

fibrinogen level

A

used to assess for DIC

17
Q

blasts greater than 20% (for non erythroid)

A

acute leukemia (AML or ALL)

18
Q

majority of AML prognoses

A

not good or poor

19
Q

therapy for non-APL AML

A

induction: 7+3 with ara-C and daunorubicin

20
Q

tear drop cells

A

myelofibrosis (type of MPD)

21
Q

myelofibrosis–what happens with RBCs, WBCs, platelets?

A

cannot be produced as well b/c bone marrow is fibrosed

get leukoerythroblastic smear

22
Q

JAK2 mutation is frequently encountered in which group of diseases

A

MPN

PV-100%
essential thrombocythemia-50%
primary myelofibrosis-50%

CML is the only exception–has PHiladelphia chromosome