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. 2019;20(10):3121–3127. doi: 10.31557/APJCP.2019.20.10.3121

Table 1.

Descriptive Data for Our AML Patients

Variable No (%)
Sex
Male 18 (35 %)
Female 34 (65 %)
Age
Median (range) 43 (19-70)
<50 years 37 (71 %)
≥50years 15 (29 %)
TLCs (x 109/L)
mean±SD 49.6±87.2
< 50 38/52* (73%)
≥ 50 14/52 (27%)
HB (gm/dL)
mean±SD 7.8± 1.9
< 8 30/52 (58%)
≥ 8 22/52 (42%)
Platelets (x 109/L)
mean±SD 77.6± 141.5
< 50 39/52 (75%)
≥ 50 13/52 (25%)
Percent of Peripheral blood blasts
mean±SD 46.1 %±27.3
< 50 23/52 (44%)
≥ 50 29/52 (56%)
B.M cellularity
Hypercellular 39/52(75%)
Normocellular 13/52(25%)
Percent of BM blasts
mean±SD 60.5 %± 23.1
<50% 14/52 (27%)
≥50% 38/52 (73%)
Immunophenotyping markers
Myeloid 34/52 (65.4%)
Myeloid with CD4 and CD14 11/52 (21%)
Myeloid with aberrant CD7 3/52 (5.8%)
Myeloid with aberrant CD19 2/52 (3.8%)
Myeloid with aberrant CD56 1/52 (1.9%)
Myeloid with CD61 1/52 (1.9%)
CD 34+ve 32/52 (62%)
CD 34 –ve 20/52 (38%)
Cytogenetics
No mitosis 10/39** (25.6%)
Normal karyotype 9/29*** ( 31.1 % )
t (9; 22) 5/29 (17.2 %)
t (8;21) 3/29 (10.3%)
t (15;17) 4/29(13.8 %)
Complex karyotyping 8/29 (27.6 %)

*52 is the total number of AML cases; **39 is the total number of AML cases undergoing cytogenetic analysis; ***29 is the total number of AML cases undergoing cytogenetic analysis after exclusion of cases showing no mitosis.