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Infant acute lymphoblastic leukemia with t(11;16)(q23;p13.3) and lineage switch into acute monoblastic leukemia.
- 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.
- Subjects :
- Bone Marrow Cells pathology
Humans
In Situ Hybridization, Fluorescence
Infant
Karyotyping
Leukemia, Monocytic, Acute pathology
Male
Metaphase
Precursor Cell Lymphoblastic Leukemia-Lymphoma pathology
Cell Lineage
Chromosomes, Human, Pair 11 genetics
Chromosomes, Human, Pair 16 genetics
Leukemia, Monocytic, Acute genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma genetics
Translocation, Genetic genetics
Subjects
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