Tranlocations, Characteristics, Immunophenotypes Flashcards

1
Q

t(8:21)

A

AML

RUN-RUN

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2
Q

inv(16:16)

A

Acute Myelomonocytic Leukemia

CBFB-MYH11

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3
Q

t(15;17)

A

Acute Promyelocytic Leukemia

PML-RARA

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4
Q

t(9;22)

A

BCL-ABR

Seen in CML and ALL

CML= good prognosis
B-cell ALL = bad prognosis

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5
Q

1(11;19)

A

B-cell ALL

MLL rearrangement

Poor prognosis

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6
Q

t(12;21)

A

B-cell ALL

Good prognosis

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7
Q

Name the 4 potential Etiologies of CLL/SLL and designate a good or bad prognosis.

A

Del 13 - good
Trisomy 12
Del 11
Del 17p - bad

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8
Q

What are the 2 cell markers that indicate somatic hypermutation in CLL memory B’s? What does that mean for the prognosis?

A

Zap-70

CD38+

Bad prognosis

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9
Q

t(11;14)

A

Mantle Cell Lymphoma

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10
Q

Popcorn cell

A

Nodular Lymphocyte Dominant Hodgkin Lymphoma

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11
Q

Cyclin D1 overexpression

Positive Ki67 stain

A

Mantle Cell Lymphoma

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12
Q

Smudge cells

A

CLL

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13
Q

Single Auer rods

A

AML Run-Run t(8;21)

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14
Q

Piles of Auer Rods

A

APL RARA t(15;17)

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15
Q

c-KIT mutation

Tryptase Positive immunophenotype

A

Mastocytosis

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16
Q

Positive Reticulin stain in the bone marrow

A

Primary Myelofibrosis

17
Q

Decreased EPO, but increased RBC count/HCT

A

Polycythemia Vera

18
Q

Main symptom = erythromyalgia

Treatment = hydroxyurea

A

Essential Thrombocythemia

19
Q

You can’t do an allogenic stem cell transplant for these 2 diseases.

A

Aplastic anemia and myelodysplasia.

The stem cells are already messed up.

20
Q

This cancer has a bimodal age distribution.

A

B-cell ALL

t(9;22)

21
Q

This form of ALL is most common in infants <1 yr.

A

t(11;19) MLL

22
Q

Only leukemia without lymphadenopathy.

TRAP stain, fried egg marrow

A

Hairy Cell Leukemia

23
Q

A kid comes in with a mediastinal mass on his X-ray, fever, anemia, and thrombocytopenia. You automatically think…..

A

T-cell ALL

24
Q

R-S Cells

A

Hodgkins Lymphoma

25
Q

t(14;18)

A

Follicular B-cell Lymphoma

26
Q

+ Bcl-2 stain IN THE GERMINAL CENTER

A

Follicular B-cell Lymphoma

27
Q

Overexpressed c-MYC due to EBV.

A

Burkitt’s Lymphoma

28
Q

How do you tell if a T cell proliferation is neoplastic rather than reactive?

A

Test for TCR clonality

29
Q

Expanded paracortex of Lymph node and random baby blood vessels interspersed.

A

Angio-immunoblastic T-cell Lymphoma

30
Q

Looks like psoriasis, but has Scezary cells floating in the bloodstream

A

Mycosis Fungiodes

31
Q

What cell does Mycosis Fungiodes infect?

A

CD4 T’s

32
Q

Congenital Version of Aplastic anemia is called….

A

Fanconi’s

33
Q

Main cause if aplastic anemia

A

Autoimmune destruction of Hematopoeitic stem cells

34
Q

Key lab finding in aplastic anemia

A

Decreased retic count with hypo cellular marrow

35
Q

Rouleaux

A

Multiple Myeloma

36
Q

IgM M-spike with no CRAB+, but hyperviscosity

A

Waldenstrom’s Macroglobulinemia

37
Q

Apple-green birefringence and congo red stain

A

Amyloidosis

38
Q

What receptor on osteoclasts do antibodies bind to cause bone lytic lesions?

A

RANK - activates them