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?

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

23
Q

Rai classification of CLL

lymphocytosis
+
lymphadenopathy

24
Q

Rai classification of CLL

lymphocytosis
\+
lymphadenopathy
\+
splenomegally
25
Rai classification of CLL ``` lymphocytosis + lymphadenopathy + splenomegally + Hgb ```
Rai 3
26
Rai classification of CLL ``` lymphocytosis + lymphadenopathy + splenomegally + Hgb ```
Rai 4
27
Binet classification system for CLL: lymphocytosis +/- 1-3 sites of lymphadenopathy
A
28
Binet classification of CLL: lymphocytosis + > 3 sites of lymphadenopathy
B
29
Binet classification of CLL: lymphocytosis + anemia and/or thrombocytopenia
C
30
CLL cytogenetic abnormalities:
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
Flow cytometry marker for poorer prognosis of CLL:
CD38+ = unmutated Ig genes (9 yrs median survival)
32
Flow cytometry marker for better prognosis of CLL:
CD38(-) = mutated Ig genes (>20 yrs median survival)
33
ZAP-70+ = ________ prognosis for CLL.
Poorer
34
ZAP-70 expression correlates with:
Ig Vh gene mutations CD38+ expression
35
Smudge cells are associated with what cytogenic abnormality in CLL and indicate _________ prognosis.
13q(-) good
36
Something that should be on your DDX with pure red cell aplasia?
parvovirus infx
37
Really good tx for CLL but big financial toxicity?
Ibrutinib