Background. We hereby describe what we believe to be the first reported case of t (1;
15)(q32; q13) associated with acute myeloid leukemia (AML). Methods. PubMed, Embase …

Background Acute myelogeneous leukemia (AML) is a malignancy of the hematopoietic
stem cells, for which cytogenetic analysis is still one of the most important diagnostic and …

Abstract The translocation: t (8; 21), a RUNX1-RUNX1T1 fusion transcript is one of the most
common chromosomal abnormality, seen in 5%–10% cases of acute myeloid leukemia …

Chromosomal rearrangements involving one donor chromosome and two or more recipient
chromosomes are called jumping translocations. To date only few cases of acute myeloid …

We report a case of acute myeloid leukemia (AML), M2 subtype according to the French-
American-British (FAB) classification, with extramedullary myeloblastoma of the uterus and a …

Although defined by the presence of t (9; 22), chronic myelogenous leukemia (CML) can
have other concurrent additional cytogenetic changes, especially during disease …

Previous small series have suggested that acute myeloid leukemia with t (8; 16) is a distinct
morphologic and clinical entity associated with poor prognosis. We describe 18 patients with …

Abstract T (8; 9) is a relatively new translocation that has been reported in a few patients with
chronic myeloid leukemia (CML) but never in acute myeloid leukemia (AML). We report here …

In this paper, we report on a 9-year-old girl with acute nonlymphocytic leukemia (FAB-M5)
with a rare chromosome abnormality, t (11; 23)(q21; p11). Peripheral blood showed Hb 7.5 …