| Literature DB >> 28906004 |
Nathalie Douet-Guilbert1,2,3, Aurelie Chauveau4, Nadia Gueganic1,2, Gaëlle Guillerm5, Corine Tous3, Marie-Josee Le Bris3, Audrey Basinko2,3, Frederic Morel1,2,3, Valerie Ugo1,4, Marc De Braekeleer1,2,3.
Abstract
Inv(16)(p13q22) and t(16;16)(p13;q22) are cytogenetic hallmarks of acute myelomonoblastic leukaemia, most of them associated with abnormal bone marrow eosinophils [acute myeloid leukaemia French-American-British classification M4 with eosinophilia (FAB AML-M4Eo)] and a relatively favourable clinical course. They generate a 5'CBFB-3'MYH11 fusion gene. However, in a few cases, although RT-PCR identified a CBFB-MYH11 transcript, normal karyotype and/or fluorescent in situ hybridization (FISH) analyses using commercially available probes are found. We identified a 32-year-old woman with AML-M4Eo and normal karyotype and FISH results. Using two libraries of Bacterial Artificial Chromosome clones on 16p13 and 16q22, FISH analyses identified an insertion of 16q22 material in band 16p13, generating a CBFB-MYH11 type A transcript. Although very rare, insertions should be searched for in patients with discordant cytological and cytogenetic features because of the therapeutic consequences.Entities:
Keywords: acute myelomonoblastic leukaemia; chromosome 16; insertion
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Year: 2015 PMID: 28906004 DOI: 10.1002/hon.2268
Source DB: PubMed Journal: Hematol Oncol ISSN: 0278-0232 Impact factor: 5.271