Myeloid Flashcards
Flow apml
-ve hla-dr and CD 34
Strong CD 33, heterogenous cd13
CD 117 usually expressed
Aberrant cd2& CD 56 - worse prog
Flow acute mast cell leukaemia
CD 13, CD 33 cd 68 cd117
M7
Cytoplasmic blebs Antigène of vwf and CD 42(go 1b) CD 41(go IIb/IIIa) on blasts Usually dry tap common Phénotype in Down syndrome
What do eukaemic pro myélocytes stain intensely with
Sudan black and mpo
Other translocation partners for RAR alpha
5:17- npm-rar fusion
3:17 tblr- rar
Both of these retinoids responsive
11;17 only one that isn’t it- usually lack Ayer rods and has CD 56 exp
Monosomal karyotype
two or more autosomal monosomies or a single autosomal monosomy plus a structural abnormality)
Which molecular mutations are associated with normal karyotype in aml
NPM1, CEBPA, FLT3-ITD, DNMT3A, IDH1,orIDH2
Favourable risks
sFavorablet(8;21)(q22;q22.1); RUNX1-RUNX1T1
inv(16)(p13.1q22) or t(16;16)(p13.1;q22); CBFB-MYH11
Mutated NPM1 without FLT3-ITD or with FLT3-ITDlow
Biallelic mutated CEBPA
Intermediate risk
Mutated NPM1 and FLT3-ITDhigh allelic ratio
Wild-type NPM1 without FLT3-ITD or with FLT3-ITDlow allelic ratio (w/o adverse-risk genetic lesions)
t(9;11)(p21.3;q23.3); MLLT3-KMT2a
Cytogenetic abnormalities not classified as favorable or adverse
Poor risk
t(6;9)(p23;q34.1); DEK-NUP214 t(v;11q23.3); KMT2Arearranged t(9;22)(q34.1;q11.2); BCR-ABL1 inv(3)(q21.3q26.2) or t(3;3)(q21.3;q26.2); GATA2,MECOM(EVI1) −5 or del(5q); −7; −17/abn(17p) Complex karyotype monosomal karyotype cWild-type NPM1 and FLT3-ITD high Mutated RUNX1d Mutated ASXL1d Mutated TP53e