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Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia

  • Sheila N.J. Sait
  • , Melinda A. Claydon
  • , Jeffrey M. Conroy
  • , Norma J. Nowak
  • , Maurice Barcos
  • , Maria R. Baer
  • Clinical Cytogenetics Laboratory

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Reciprocal chromosomal translocations involving the MLL gene at chromosome region 11q23 are recurring cytogenetic abnormalities in both de novo and therapy-related acute myeloid leukemia (AML) and in acute lymphoblastic leukemia. We report a t(4;11)(p12;q23) with rearrangement of MLL and FRYL (also known as AF4p12), a human homolog to the furry gene of Drosophila, in an adult patient with therapy-related AML after fludarabine and rituximab therapy for small lymphocytic lymphoma and radiation therapy for breast carcinoma. To our knowledge, t(4;11)(p12;q23) has been reported in two previous patients, and MLL and FRYL rearrangement was demonstrated in one of them. Both of the previous patients had therapy-related leukemias after exposure to topoisomerase II inhibitors, whereas our patient had received cytotoxic therapy that did not include a topoisomerase II inhibitor. Thus, t(4;11)(p12;q23) with MLL and FRYL involvement represents a new recurring 11q23 translocation, to date seen only in therapy-related acute leukemias.

Original languageEnglish
Pages (from-to)143-146
Number of pages4
JournalCancer Genetics and Cytogenetics
Volume177
Issue number2
DOIs
StatePublished - Sep 2007

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