A case of acute myeloid leukemia with a translocation between chromosome 1 and 18 is
described. The patient was a 21-year-old male with a 2-week history of fever and fatigue …

“Simple” variants of the t (8; 21) translocation involving chromosome 8 and a chromosome
other than number 21 are rare. To our knowledge, only t (3; 8)(q29; q22), t (8; 11)(q22; q13) …

Abstract Acute Myelogeneous Leukemia (AML) is a heterogeneous disease with respect to
morphology, immunophenotype, and genetic rearrangements. Multiple recurrent …

We report a case of a patient aged about 53 years, who initially presented with
hematological disorders (WBC: 44000/mm3, Hb: 11g/dl, Pit: 127000/mm3) without tumoral …

Chromosome 21 and in particular band 21q22, the site of AML1 (RUNX1, CBFA2) gene, is
among the most frequent targets of chromosomal translocations in leukemia observed in …

The complex variants of t (8; 21) involving chromosomes 8 and 21 as well as a variable
chromosome account for 1.1∼ 5% of acute myeloid leukemia (AML) patients. This paper …

Trisomy 22 has been reported frequently as a recurring secondary abnormality in acute
myelocytic leukemia (AML), particularly associated with inv (16)(p13q22)[1]. Trisomy 22 as a …

We present an 18-year-old woman who was diagnosed with acute myeloblastic leukemia
(AML M2), and in whom chromosome analysis of bone marrow cells revealed t (7; 11), an …

Many AML-associated chromosomal abnormalities, such as t (8; 21), t (15; 17), inv (16), t (9;
11), t (9; 22) and t (6; 9) are well known. The chromosomal aberration of t (16; 21)(p11; q22) …