Two cases of acute myeloid leukemia with t(11;17) associated with varying morphology and immunophenotype: Rearrangement of the MLL gene and a region proximal to the RARα gene

Department of Pediatrics, University of North Carolina at Chapel Hill, North Carolina, United States
Cancer Genetics and Cytogenetics (Impact Factor: 1.93). 07/2005; 159(2):168-73. DOI: 10.1016/j.cancergencyto.2004.10.009
Source: PubMed


This report describes 2 cases of acute myeloid leukemia (AML), which based on the WHO classification would be classified as AML with an 11q23 (MLL) abnormality, but with contrasting morphologic and immunophenotypic profiles. One case had monocytic features (morphologically and immunophenotypically) with a t(11;17)(q23;q21), a previously identified variant translocation in acute promyelocytic leukemia (APL). The second case had morphologic and immunophenotypic features of APL associated with a t(11;17)(q23;q25). In both cases, fluorescence-in-situ hybridization (FISH) analysis demonstrated that the 11q23 breakpoint involved the MLL gene, but RARalpha was not involved in the 17q breakpoints. These cases illustrate the importance of FISH analysis to confirm the presence of a particular recurring rearrangement.

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Available from: Cherie Dunphy, Jan 04, 2014
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    • "Kang et al. [9] reported 2 cases of acute myeloid leukemia with t(11;17) associated with varying morphology and immunophenotype. Their first case had a prominent monocytic component based on flow cytometric analysis and nonspecific esterase staining of BM core biopsy touch preparations. "
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