A chromosome study on 97 cases of acute nonlymphocytic leukemia M2
Chen Fan-jun , Yang Ai-de , Fei Hong-bao
Current Medical Science ›› 1994, Vol. 14 ›› Issue (1) : 35 -37.
Chromosomal studies were performed in the same laboratory on 97 untreated cases of de novo acute nonlymphocytic leukemia M2. The overall incidence of chromosomal abnormality was 70. 1% (68 out of 97 cases), which was higher in children (84. 2%) than in adults (61%). The male to female chromosomal abnormality ratio was nearly the same (male 71% and female 68.4%,P > 0. 05). Hypodiploidy was the most common numerical abnormality (39%) and t (8; 21) was the most common structural abnormality (48.1%). In the patients with t(8; 21), 64. 5% (20 out of 31 cases) male lost chromosome Y (-Y) and 33% (5 out of 15 cases) female lost one chromosome X (-X).
acute nonlymphocytic leukemia M2 / chromosome
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