Tranlocations, Characteristics, Immunophenotypes Flashcards
t(8:21)
AML
RUN-RUN
inv(16:16)
Acute Myelomonocytic Leukemia
CBFB-MYH11
t(15;17)
Acute Promyelocytic Leukemia
PML-RARA
t(9;22)
BCL-ABR
Seen in CML and ALL
CML= good prognosis
B-cell ALL = bad prognosis
1(11;19)
B-cell ALL
MLL rearrangement
Poor prognosis
t(12;21)
B-cell ALL
Good prognosis
Name the 4 potential Etiologies of CLL/SLL and designate a good or bad prognosis.
Del 13 - good
Trisomy 12
Del 11
Del 17p - bad
What are the 2 cell markers that indicate somatic hypermutation in CLL memory B’s? What does that mean for the prognosis?
Zap-70
CD38+
Bad prognosis
t(11;14)
Mantle Cell Lymphoma
Popcorn cell
Nodular Lymphocyte Dominant Hodgkin Lymphoma
Cyclin D1 overexpression
Positive Ki67 stain
Mantle Cell Lymphoma
Smudge cells
CLL
Single Auer rods
AML Run-Run t(8;21)
Piles of Auer Rods
APL RARA t(15;17)
c-KIT mutation
Tryptase Positive immunophenotype
Mastocytosis
Positive Reticulin stain in the bone marrow
Primary Myelofibrosis
Decreased EPO, but increased RBC count/HCT
Polycythemia Vera
Main symptom = erythromyalgia
Treatment = hydroxyurea
Essential Thrombocythemia
You can’t do an allogenic stem cell transplant for these 2 diseases.
Aplastic anemia and myelodysplasia.
The stem cells are already messed up.
This cancer has a bimodal age distribution.
B-cell ALL
t(9;22)
This form of ALL is most common in infants <1 yr.
t(11;19) MLL
Only leukemia without lymphadenopathy.
TRAP stain, fried egg marrow
Hairy Cell Leukemia
A kid comes in with a mediastinal mass on his X-ray, fever, anemia, and thrombocytopenia. You automatically think…..
T-cell ALL
R-S Cells
Hodgkins Lymphoma