Acute leukemias with thrombocytosis have been recently linked with structural abnormalities
of the short arm of chromosome 3. A 46‐year‐old man with a 2‐month history of recurrent …

Abstract The translocation t (8; 21)(q22; q22), which results in the fusion of the AML1
(RUNX1) and ETO (CBFA2T1) genes, is a recurrent aberration in acute myeloid leukemia …

Variants of the t (8; 21)(q22; q22) involving chromosome 8, 21, and other chromosomes
account for about 3% of all t (8; 21)(q22; q22) in acute myeloid leukemia (AML) patients. We …

We report the case of an 11-year-old girl who was initially diagnosed with a chronic
myeloproliferative disorder, possibly chronic myelogenous leukemia (CML), based on …

Acute myeloid leukemia (AML) is a clinically and molecularly heterogeneous disease
characterized by the aberrant proliferation of myeloid stem cells, reduced apoptosis and …

The authors report a unique translocation in a patient with M7 acute myeloid leukemia and
review the literature. A 22-month-old girl without Down syndrome was diagnosed with acute …

Acute myeloid leukemia with maturation (AML-M2 based on the French-American-British
classification) is often accompanied by typical chromosomal changes such as t (8; 21)(q22; …

One of the most frequent structural chromosomal anomaly is t (8; 21)(q22; q22) that occurs in
approximately 5-15% of all acute myeloid leukemia (AML). However, t (3; 21)(p21; q22) and …

One of the most frequent structural chromosomal anomaly is t (8; 21)(q22; q22) that occurs in
approximately 5-15% of all acute myeloid leukemia (AML). However, t (3; 21)(p21; q22) and …

Granulocytic sarcoma is a form of acute myeloid leukemia which may occur in any
anatomical site. Isolated pancreatic granulocytic sarcoma is however, extremely rare …