[Acute myeloid leukemia with t(8;21): unusual cytological presentation and immunophenotype].
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This report describes a case of t (15; 17) acute promyelcytic leukaemia (APL, FAB subtype
M3) with dysgranulopoiesis at diagnosis in a patient who developed myelodysplasia (MDS) …

Here, we describe for the first time an acute myeloid leukemia (AML) case with two distinct
cytogenetic abnormalities, namely t (11; 20)(p15; q11. 2) and del (9q), combined together …

t (3; 21)(q26; q22) is a recurrent chromosomal abnormality in Philadelphia‐positive chronic
myeloid leukaemia in blast crisis and in treatment‐related myelodysplastic syndrome and …

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 …

Background: Rare subgroups of pediatric patients with acute myeloid leukemia (AML), such
as t (16: 21)(p11; q22), require international cooperation to establish a proper stratification …

Background Acute myeloid leukemia (AML) with specific balanced 5q33 translocations are
classified as AML with myelodysplasia-related changes regardless of their morphologic …

We describe two patients with CML blast crisis with clonal evolution affecting 16q22 (t (16;
16)(p13; q22) and inv (16)(p13; q22), abnormalities of core binding factor, usually found in …

A 66-year-old Chinese man was admitted to our hospital in September 2006 because of
shortness of breath and palpitation after exertion, which was exacerbated and accompanied …

Abstract The t (7; 11)(p15; p15) translocation has been reported as a rare and recurrent
chromosomal abnormality in acute myeloid leukemia (AML) patients. The NUP98‐HOXA9 …