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Infant acute lymphoblastic leukemia with t(11;16)(q23;p13.3) and lineage switch into acute monoblastic leukemia.

Authors :
Stasik C
Ganguly S
Cunningham MT
Hagemeister S
Persons DL
Source :
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 2006 Jul 15; Vol. 168 (2), pp. 146-9.
Publication Year :
2006

Abstract

Rearrangements of the mixed-lineage leukemia (MLL) gene have been associated with a poor prognosis in infant acute lymphoblastic leukemia (ALL). Previously, MLL translocations involving the CREP-binding protein (CREBBP) gene at chromosome band 16p13.3 have primarily been reported in treatment-related acute myeloid leukemia, after chemotherapy for other primary malignancies using topoisomerase II inhibitors. We report a case of de novo infant ALL with t(11;16)(q23;p13.3). After chemotherapy, this patient developed an acute monoblastic leukemia (M5b) with retention of the t(11;16)(q23;p13.3), indicating that this is a lineage switch of the original leukemic clone. To our knowledge, these findings have not been previously reported.

Details

Language :
English
ISSN :
0165-4608
Volume :
168
Issue :
2
Database :
MEDLINE
Journal :
Cancer genetics and cytogenetics
Publication Type :
Academic Journal
Accession number :
16843104
Full Text :
https://doi.org/10.1016/j.cancergencyto.2006.02.013