Title
Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion
Date Issued
01 August 2005
Access level
metadata only access
Resource Type
journal article
Author(s)
Jahn J.A.
Scheerle J.
Eid M.
Meister R.J.
Christie R.J.
Croft C.D.
Wallingford S.
Heritage D.W.
Mowrey P.N.
Meloni-Ehrig A.M.
Quest Diagnostics Nichols Institute
Abstract
Fluorescence in situ hybridization (FISH) analysis of the bone marrow of a 24-year-old man diagnosed with acute promyelocytic leukemia (APL) revealed a variant pattern with one fusion signal instead of the typical two fusions expected with the probe set used. The combined FISH and conventional chromosome analyses suggested that two subsequent translocations had occurred in this patient involving the same chromosomes 15 and 17. As the prognostic outcome in APL is strictly associated with the presence of a PML/RARA fusion, it is useful and necessary to perform both cytogenetic and FISH analyses of a variant t(15;17) to determine the status of the PML/RARA fusion. © 2005 Elsevier Inc. All rights reserved.
Start page
70
End page
73
Volume
161
Issue
1
Language
English
OCDE Knowledge area
Oncología
Genética humana
Scopus EID
2-s2.0-23244447162
PubMed ID
Source
Cancer Genetics and Cytogenetics
ISSN of the container
01654608
Sources of information:
Directorio de Producción Científica
Scopus