Two rare cases of acute myeloid leukemia with t (8; 16)(p11. 2; p13. 3) and 1q duplication: case presentation and literature review

M Liu, Y Ren, X Wang, X Lu, M Li, YM Kim, S Li… - Molecular …, 2020 - Springer
Background Acute myeloid leukemia (AML) is a complex hematological disease
characterized by genetic and clinical heterogeneity. The identification and understanding of …

Unusual karyotype in acute myelomonocitic leukemia: a case report

ML Consoli, A Romano, NL Parrinello… - Anticancer …, 2019 - ar.iiarjournals.org
Background/Aim: Acute myeloid leukemia is well characterized by chromosomal aberrations
that correspond to various subtypes of acute leukemias. The t (8; 21)(q22; q22) is a frequent …

Identification of t (15; 17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2

S Li, L Zhang, WF Kern, D Andrade, JE Forsberg… - Cancer genetics and …, 2002 - Elsevier
A 32-year-old man was newly diagnosed with acute myelocytic leukemia, classified as acute
myeloblastic leukemia with maturation (AML-M2) according to the French–American–British …

Acute myeloid leukemia with recurrent cytogenetic abnormalities

K Foucar, J Anastasi - American Journal of Clinical Pathology, 2015 - academic.oup.com
Abstract Objectives: Session 1 of the 2013 Society for Hematopathology/European
Association for Hematopathology Workshop was devoted to the cases of acute myeloid …

A translocation between 3q21 and 12q24 in a patient with minimally differentiated acute myeloid leukemia (AML-MO)

N Yamagata, C Shimazaki, T Kikuta, H Hirai… - Cancer genetics and …, 1997 - Elsevier
Only a small number of reports have described the cytogenetic analysis of minimally
differentiated acute myeloid leukemia (AML, MO). We performed a cytogenetic analysis on a …

A rare translocation (4; 11)(q21; p14–15) in an acute lymphoblastic leukemia expressing T-cell and myeloid markers

JE Hardingham, GB Peters, A Dobrovic… - Cancer genetics and …, 1991 - Elsevier
A 21-year-old male presented with a large mediastinal mass and a white cell count of 420×
10 9/L. A diagnosis of acute lymphoblastic leukemia (ALL) was made, with 90% of cells in …

Acute leukaemia and myelodysplastic syndromes with chromosomal rearrangement involving 11q23 locus, but not MLL gene

W Zuo, SA Wang, C DiNardo, M Yabe, S Li… - Journal of Clinical …, 2017 - jcp.bmj.com
Aims Chromosome 11q23 translocations, resulting in MLL (KMT2A) rearrangement, have
been well characterised in acute myeloid leukaemia (AML) and acute lymphoblastic …

A recurrent translocation, t (3; 11)(q21; q13), found in two distinct cases of acute myeloid leukemia

JC Cigudosa, MJ Calasanz, MD Odero, J Marin… - Cancer genetics and …, 1995 - Elsevier
A Recurrent Translocation, t(3;11)(q21;q13), Found in Two Distinct Cases of Acute Mye|oid
Leukemia Page 1 ELSEVIER A Recurrent Translocation, t(3;11)(q21;q13), Found in Two …

Clinical characteristics and laboratory analyses of acute myeloid leukemia with t (16; 21)(p11; q22)

Z Zhang, J Zou, Y Li, Z Liu, R Xu, W Tian… - Oncology …, 2015 - spandidos-publications.com
The present study reviewed three patients with acute myeloid leukemia (AML) who had the
specific genetic abnormality t (16; 21)(p11; q22). To investigate the clinical and laboratory …

A t (6; 14; 9)(p22; q22; q34) three‐way translocation: Description of a cytogenetically visible variant t (6; 9) in acute myeloid leukemia

AC Smith, D Maze, D Xia… - American Journal of …, 2022 - Wiley Online Library
DEK-NUP214 is a recurrent, but relatively rare translocation in myeloid neoplasia ($0.7–2%)
1, 2 associated with a poor prognosis in acute myeloid leukemia (AML) and myelodysplastic …