Author(s): Movafagh A, Varma N, Varma S
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Abstract We describe a case of acute promyelocytic leukemia ANLL-M3 with association of t(15;17) and t(8;21) and various chromosomal aberrations. Clinically, immunologically, and morphologically, our patient fits the diagnosis of typical ANLL-M3. The co-existence of two specific FAB chromosomal translocations in a single leukemic clone is rare. The rarity of this association enhances the significance of this report.
This article was published in Ann Hematol
and referenced in Journal of Cancer Science & Therapy