Volume 24, Issue 2 pp. 151-155
Brief Communication

MLL is involved in a t(2;11)(p21;q23) in a patient with acute myeloblastic leukemia

E.W. Fleischman

E.W. Fleischman

Cancer Research Center, Moscow, Russia

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S. Reshmi

S. Reshmi

University of Chicago Medical Center, Section of Hematology/Oncology, Chicago, Illinois

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M.A. Frenkel

M.A. Frenkel

Cancer Research Center, Moscow, Russia

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W.I. Konovalova

W.I. Konovalova

Cancer Research Center, Moscow, Russia

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G.P. Guleva

G.P. Guleva

Cancer Research Center, Moscow, Russia

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O.E. Kulagina

O.E. Kulagina

Cancer Research Center, Moscow, Russia

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L.N. Konstantinova

L.N. Konstantinova

Cancer Research Center, Moscow, Russia

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N.N. Tupitsyn

N.N. Tupitsyn

Cancer Research Center, Moscow, Russia

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J.D. Rowley

Corresponding Author

J.D. Rowley

University of Chicago Medical Center, Section of Hematology/Oncology, Chicago, Illinois

University of Chicago Medical Center, Section of Hematology/Oncology, 5841 S. Maryland Ave., MC 2115, Chicago, IL 60637–1470.Search for more papers by this author

Abstract

We describe a patient with acute myeloblastic leukemia (AML-M0) whose cells had a t(2;11)(p21;q23). Fluorescence in situ hybridization analysis with a probe for MLL showed that it was split, hybridizing to both the derivative 2 and 11 chromosomes. Nineteen other patients with 2p;11q translocations have been described; breakpoints in 14 of these are the same as in the case we describe. The phenotype of these patients is quite variable, with 14 patients having myelodysplastic syndrome which evolved to AML in six. Four patients had AML and two had acute lymphoblastic leukemia. MLL status has been studied in two other patients; one had MLL rearranged and one did not. Genes Chromosomes Cancer 24:151–155, 1999. © 1999 Wiley-Liss, Inc.

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