Acute myeloid leukemia with the translocation (8; 16)(p11; p13) is a rare type of acute
leukemia with a number of unique features including erythrophagocytosis, extramedullary …

The t (7; 11)(p15; p15) translocation is a recurrent genetic abnormality associated with acute
myelogenous leukemia (AML). The translocation results in a fusion between the nucleoporin …

Recurrent genetic abnormalities are important prognostic markers in acute myeloid
leukemias (AML). The World Health Organization classification recognizes 7 categories of …

Discussion: Some 60 cases of AML with t (7; 11)(p15; p15) have been reported.
Interestingly, most of the cases involved Asians, especially Japan and China. As the …

Acute myelogenous leukemia (AML) with the translocation t (6; 9)(p23; q34) is a rare
disease entity with a poor prognosis. We report three patients; two were diagnosed with AML …

Background: Acute myeloid leukemia (AML) is a heterogeneous group of malignant
neoplasm of hematopoietic disorders characterized by an abnormal proliferation of myeloid …

Objective To investigate the clinical and laboratory characteristics of acute myeloid leukemia
(AML) with t (16; 21)(p11; q22) translocation. Methods Two patients diagnosed by …

Cytogenetic abnormalities play an important role in diagnosis, classification and prognosis
in acute myeloid leukemia (AML). Nevertheless, several chromosome abnormalities have …

Acute myeloid leukemia (AML) patients with t (8; 16)(p11. 2; p13) constitute a small
subgroup with a distinct genetic and clinical profile. We present a unique case of a female …

We present a novel, rare but recurrent variant three way translocation of t (8; 21), t (8; 16;
21)(q22; q24; q22), as a primary cytogenetic abnormality, resulting in AML1/ETO fusion …