Congenital MLL-positive B-cell acute lymphoblastic leukemia (B-ALL) switched lineage at relapse to acute myelocytic leukemia (AML) with persistent t(4;11) and t(1;6) translocations and JH gene rearrangement

Jie-Gen Jiang Department of Pathology, Columbia University, New York, USA; Department of Pathology, Columbia University, New York, USA

Elizabeth Roman Department of Pathology, Columbia University, New York, USA; Department of Pathology, Columbia University, New York, USA

Subhadra V Nandula Department of Pathology, Columbia University, New York, USA; Department of Pathology, Columbia University, New York, USA

Vundavalli VS Murty Department of Pathology, Columbia University, New York, USA; Department of Pathology, Columbia University, New York, USA

Govind Bhagat Department of Pathology, Columbia University, New York, USA; Department of Pathology, Columbia University, New York, USA

Bachir Alobeid Department of Pathology, Columbia University, New York, USA; Department of Pathology, Columbia University, New York, USACorrespondence[email protected]

Congenital MLL-positive B-cell acute lymphoblastic leukemia (B-ALL) switched lineage at relapse to acute myelocytic leukemia (AML) with persistent t(4;11) and t(1;6) translocations and JH gene rearrangement

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Congenital MLL-positive B-cell acute lymphoblastic leukemia (B-ALL) switched lineage at relapse to acute myelocytic leukemia (AML) with persistent t(4;11) and t(1;6) translocations and JH gene rearrangement

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