The first case of acute myeloid leukemia with solitary t(6;7)(p21.3;p22) passenger translocation that developed at relapse after allogeneic hematopoietic stem cell transplantation in a patient with a normal karyotype at the initial diagnosis-Reference-Cited by-同舟云学术

The first case of acute myeloid leukemia with solitary t(6;7)(p21.3;p22) passenger translocation that developed at relapse after allogeneic hematopoietic stem cell transplantation in a patient with a normal karyotype at the initial diagnosis

Published:2016 Issue:4 Volume:51 Page:279
ISSN:2287-979X
Container-title:Blood Research
language:en
Short-container-title:Blood Res

Author:

Park Sang Hyuk¹²,Lee Eun Yup¹²,Shin Ho-Jin²³

Affiliation:

1. Department of Laboratory Medicine, Pusan National University School of Medicine, Pusan National University Hospital, Busan, Korea.

2. Biomedical Research Institute, Pusan National University School of Medicine, Pusan National University Hospital, Busan, Korea.

3. Division of Hematology-Oncology, Department of Internal Medicine, Pusan National University School of Medicine, Pusan National University Hospital, Busan, Korea.

Publisher

The Korean Society of Hematology

Subject

Hematology

Link

https://synapse.koreamed.org/pdf/10.5045/br.2016.51.4.279

Reference13 articles.

1. 5‘RUNX1-3’USP42 chimeric gene in acute myeloid leukemia can occur through an insertion mechanism rather than translocation and may be mediated by genomic segmental duplications

2. Whole transcriptome sequencing of a paediatric case ofde novoacute myeloid leukaemia with del(5q) revealsRUNX1-USP42andPRDM16-SKIfusion transcripts

3. Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review

4. Myeloid leukemia with t(7;21)(p22;q22) and 5q deletion

5. A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity