Title
Cryptic ins(4;11)(q21;q23q23) detected by fluorescence in situ hybridization: a variant of t(4;11)(q21;q23) in an infant with a precursor B-cell acute lymphoblastic leukemia report of a second case
Date Issued
15 April 2007
Access level
metadata only access
Resource Type
journal article
Author(s)
Meloni-Ehrig A.M.
Edwards T.
Scheerle J.
Burks K.
Repetti C.
Christacos N.C.
Kelly J.C.
Greenberg J.
Murphy C.
Croft C.D.
Heritage D.
Mowrey P.N.
Quest Diagnostics Nichols Institute
Publisher(s)
Elsevier
Abstract
We report the chromosomal findings in a 4-year-old female with precursor B-cell acute lymphoblastic leukemia (ALL). The diagnostic karyotype showed an isochromosome 7q, i(7)(q10), as well as questionable rearrangements on 9p and 11q. Fluorescence in situ hybridization (FISH) studies on both interphase and metaphase cells using the MLL "break-apart" and the centromeric chromosome 4 probes were instrumental in the characterization of an MLL gene rearrangement, which was cryptic by conventional cytogenetic analysis. Specifically, the FISH pattern was consistent with an insertion of the 5' region of the MLL gene into chromosome 4 at band q21, most likely a variant t(4;11)(q21;q23). This is the second case of FISH detection of an ins(4;11) in ALL. Our case exemplifies the importance of FISH in the further characterization of precursor B-cell ALL cases without any apparent prognostically significant chromosomal abnormalities.
Start page
166
End page
169
Volume
174
Issue
2
Language
English
OCDE Knowledge area
Oncología Genética humana
Scopus EID
2-s2.0-34247101108
PubMed ID
Source
Cancer Genetics and Cytogenetics
ISSN of the container
01654608
Sources of information: Directorio de Producción Científica Scopus