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. Author manuscript; available in PMC: 2016 Jun 1.
Published in final edited form as: Clin Lymphoma Myeloma Leuk. 2014 Dec 24;15(6):358–363. doi: 10.1016/j.clml.2014.12.009

Table 2.

Cytogenetic and molecular genetic analysis in acute myelogenous leukemia patients with Sweet's Syndrome

Patient Characteristics N Percentage

Cytogenetic analysis (n=21)
    Diploid cytogenetics 7 33%
    Complex cytogenetics (≥ 3 chromosomal abnormalities) 5 24%
    −5/del(5q) (as sole abnormality) 3 14%
    t(6;9) 2 10%
    Trisomy 8 1 5%
    t(11;17) 1 5%
    t(15;17) 1 5%
    t(3;3) 1 5%

Karyotype abnormalities constituting “complex cytogenetics” (n=5)1
    −5/del(5q) 5 100%
    −3 3 60%
    −13/del(13q) 3 60%
    −7/del(7q) 2 40%
    −12 2 40%
    −17 2 40%
    Others2 1 each 20%

Molecular genetics analysis
    FLT3 (total tested = 18)
        Internal Tandem Duplication 4 22%
                D835 3 17%
    NPM1 (total tested=7) 2 28%
    RAS (total tested=13) 0 0
    C-KIT (total tested=5) 0 0
    CEBPα (total tested=3) 0 0

Abbreviations used: CG: cytogenetics; FLT3: fms-related tyrosine kinase 3; NPM1: nucleophosmin 1, RAS: rat sarcoma, C-KIT: mast/stem cell growth factor receptor Kit; CEBPα: CCAAT/enhancer binding protein alpha

1

Complex cytogenetics patients only (n=5)

2

Others: −1, del(6q), −9, −11, −12, −14, −15, del(20q), add(2p), add(3q), add(6q), add7, add(8q), +11, add(16p), add(17p), add(22q)