AML and CLL cases Flashcards

1
Q

Pre-existing diseases associated with greater risk of AML?

A

Down Syndrome

Ataxia telangiectasia

Fanconia anemia

Li Fraumeni syndrome

Wiskott-Aldrich

familial leukemia

myelodysplasia

PNH

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2
Q

Secondary AML risk from:

A

prior chemo

radiation exposure

BENZENE exposure

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3
Q

Extramedullary disease most common with which lineage of AML?

A

Monocytic

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4
Q

Biggest prognostic factor in AML?

A

CYTOGENETICS

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5
Q

“Good” risk cytogenetics of AML:

A

t(8;21)

t(16;16)

t(15;17)

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6
Q

Finding on blood smear associated with “good” prognosis of AML (M3)?

A

Lots of Auer rods

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7
Q

Intermediate prognostic factor of AML:

A

Normal karyotype with NPM1+, Flt3-

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8
Q

Unfavorable prognostic cytogenetics in AML:

A

del 5
del 7

trisomy 8

11q23

other complex karyotypes

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9
Q

Unfavorable prognostic factor in AML associated with prior chemo?

**on the test

A

11q23

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10
Q

Defining criteria of remission in AML?

A
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11
Q

Treatment given to “mop up” after remission achieved in AML:

A

Consolidation chemo

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12
Q

Contraindication for allogenic transplant?

A

age > 60

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13
Q

What is DIC? What are it’s characteristics?

A

Disseminated Intravascular Coagulation

  • coagulopathy
  • depressed fibrinogen
  • thrombocytopenia
  • FATAL hemmorrhage
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14
Q

Why is dx of acute promyelocytic leukemia (M3) time sensitive?

A

DIC is rapidly fatal

**ATRA should be given in under 6 hours

“Don’t let the sun set on M3”

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15
Q

Danger of hyperleukocytosis seen in M4?

A

Hyperviscosity –> sludging in vasculature –> ischemia and/or infarction

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16
Q

Tx for hyperleukoocytosis:

A

Leukophoresis to reduce WBC to

17
Q

What the problem with automated differentials?

A

Can mistake blast cells for monocytosis.

18
Q

Most common leukemia in adults?

A

CLL

19
Q

“Better” prognostic indicator for CLL?

A

Mutated Ig Vh genes

20
Q

Cell markers seen on flow cytometry for CLL:

**on test!!

A

CD5+

CD19+

CD20+

CD23+

21
Q

Physical exam finding for CLL:

A

Diffuse adenopathy

22
Q

Rai classification of CLL

lymphocytosis

A

Rai 0

23
Q

Rai classification of CLL

lymphocytosis
+
lymphadenopathy

A

Rai 1

24
Q

Rai classification of CLL

lymphocytosis
\+
lymphadenopathy
\+
splenomegally
A

Rai 2

25
Q

Rai classification of CLL

lymphocytosis
\+
lymphadenopathy
\+
splenomegally
\+
Hgb
A

Rai 3

26
Q

Rai classification of CLL

lymphocytosis
\+
lymphadenopathy
\+
splenomegally
\+
Hgb
A

Rai 4

27
Q

Binet classification system for CLL:

lymphocytosis +/- 1-3 sites of lymphadenopathy

A

A

28
Q

Binet classification of CLL:

lymphocytosis + > 3 sites of lymphadenopathy

A

B

29
Q

Binet classification of CLL:

lymphocytosis + anemia and/or thrombocytopenia

A

C

30
Q

CLL cytogenetic abnormalities:

A

13q (-) Best prog
I
Normal Karyotype I
I
Trisomy 12 I
I
11q (-) I
V
17q (-) Worst prog

**ALWAY get FISH, 17q(-) behaves like Mantle cell

31
Q

Flow cytometry marker for poorer prognosis of CLL:

A

CD38+ = unmutated Ig genes (9 yrs median survival)

32
Q

Flow cytometry marker for better prognosis of CLL:

A

CD38(-) = mutated Ig genes (>20 yrs median survival)

33
Q

ZAP-70+ = ________ prognosis for CLL.

A

Poorer

34
Q

ZAP-70 expression correlates with:

A

Ig Vh gene mutations

CD38+ expression

35
Q

Smudge cells are associated with what cytogenic abnormality in CLL and indicate _________ prognosis.

A

13q(-)

good

36
Q

Something that should be on your DDX with pure red cell aplasia?

A

parvovirus infx

37
Q

Really good tx for CLL but big financial toxicity?

A

Ibrutinib