AML with Recurrent Genetic Abnormalities

Immunohistochemistry in AML with Recurrent Cytogenetic Abnormalities

AML t(8;21)
Usually Positive
HLA_DR
Usually Positive (flow marker)
CD13
Usually Positive
Often Positive
Often Positive
CD79a  
May be Positve (Cytoplasmic)
-/+ (usually weak)
Occasional cases may be positive.  Adverse prognostic indicator.
 

AML inv(16) or t(16;16)
Usually Positive
Usually Positive
Often positive, but not specific
 
Varying expression of granulocytic and monocytic markers may be seen depending upon differentiation.

APL t(15;17) PML-RARA
Weak or negative
HLA_DR
Weak or negative (flow marker)
Often Positive (may be weak)
~20% of cases are positive, associated with a worse prognosis.
 

AML t(9;11) MLLT3-MLL
Variably Positive
Variably Positive
Often strong expression
 

AML t(6;9) DEK-NUP214
MPO
Often Positive
Usually Positive
Usually Positive
~50% are Positive
 

AML inv(3) or t(3;3) RPN1-EVI1
There is limited data available.  Some studies show CD7 may be aberrantly expressed.

AML t(1;22) RBM15-MKL1 (Megakaryoblastic AML)
CD41  
Often Positive
CD61
Often Positive
CD42
Mature platelet marker, which is less often expressed.
Usually Negative
MPO
Usually Negative
Negative
 

AML with Mutated NPM1
CD34 is usually negative.  Myeloid and/or monocytic markers may be positive.

AML with Mutated CEBPA
CD34  
Usually Positive
~50-73% of cases are positive
Usually negative
 
One or more myeloid markers are usually positive.
 
References