Acute myeloid leukemia with associated translocation t (15; 17) and 11q23/MLL abnormality

L Campiotti, L Appio, R Casalone, R Righi… - Leukemia & …, 2008 - Taylor & Francis
The classification of acute myeloid leukemia (AML) recognizes a subgroup of diseases with
recurring genetic abnormalities. Translocation (15; 17) is the marker of acute promyelocitic …

Translocation t (5; 18)(q35; q21) as a rare nonrandom abnormality in acute myeloid leukemia

A Daraki, LK Bourantas, KN Manola - Cytogenetic and Genome …, 2013 - karger.com
Cytogenetic abnormalities play an important role in diagnosis, classification and prognosis
in acute myeloid leukemia (AML). Nevertheless, several chromosome abnormalities have …

Translocation t (11; 19)(q23; q13. 1) without MLL rearrangement in acute myeloid leukemia: heterogeneity of the 11q23 breakpoints

K Yamamoto, S Kawamoto, S Kakiuchi… - Acta …, 2015 - karger.com
Chromosomal rearrangements involving the MLL gene (approved symbol: KMT2A) at 11q23
are associated with different types of hematological malignancies, with more than 70 fusion …

t (16; 21)(q24; q22) in acute myeloid leukemia: case report and review of the literature

CL Boils, AN Mohamed - Acta Haematologica, 2008 - karger.com
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 …

[HTML][HTML] A rare case of acute myeloid leukemia with t (12; 19)(q13; q13)

A Chebly, FG Haddad, J Bassil, T Yammine… - Leukemia Research …, 2020 - Elsevier
Acute myeloid leukemia (AML) is characterized by chromosomal abnormalities affecting
both prognosis and course of treatment. While most AML patients have well described …

Acute myeloid leukemia with t (5; 11): two case reports

M Itoh, T Okazaki, M Tashima, H Sawada… - Leukemia research, 1999 - Elsevier
A case of acute monocytic leukemia (AMoL) with t (5; 11)(q31; q23) and a case of acute
myelomonocytic leukemia (AMMoL) with t (5; 11)(q35; q13. 1) are reported. The …

Complex t (8; 14; 21)(q22; q13; q22), a variant of t (8; 21), with t (15; 21)(q15; p11) in a patient with acute myelogenous leukemia (M1)

T Takahashi, Y Maruyama, Y Satoh… - Cancer genetics …, 2004 - cancergeneticsjournal.org
The translocation (8; 21)(q22; q22) is a frequent karyotypic abnormality in acute
myelogenous leukemia (AML). Most cases of AML with t (8; 21) show an M2 phenotype …

New variant translocation (8; 20)(q22; q13) in acute myelocytic leukemia

T Shirota, N Oguchi, K Shinohara, Y Noguchi… - Cancer genetics and …, 1998 - Elsevier
A new variant translocation,(8; 20)(q22; q13) in a patient with acute myelocytic leukemia
(AML) M2 is reported. As far as we know, this is the second case of the t (8; 20) in de novo …

A novel three-way t (7; 21; 8)(q11. 2; q22; q22) in a patient with acute myeloid leukemia

SH Oh, TS Park, JR Choi, J Kim… - Cancer genetics …, 2009 - cancergeneticsjournal.org
Acute myeloid leukemia (AML) with t (8; 21)(q22; q22) is well characterized by its unique
morphology of AML-M2 subtype and favorable prognosis [1]. This recurrent translocation is …

[PDF][PDF] Morphologic characterization of acute myeloid leukemia with cytogenetic or molecular evidence of t (8; 21), t (15; 17), inv (16) and 11q23 abnormalities

M Rozman, JT Navarro, A Domingo, R Ayats… - …, 2002 - haematologica.org
We reviewed the morphology of 110 acute myeloid leukemias (AML) with recurrent
cytogenetic/molecular translocations. The t (8; 21) cases had some pseudolymphoid blasts …