Sequential acquisition of IgH and TCR rearrangements during the preleukemic phase of acute lymphoblastic leukemia in an adolescent patient.

Linden T, Furlan I, Schwarz S, Stoehr R, Niemeyer CM, Rossig C

Research article (journal)

Abstract

Acute lymphoblastic leukemia (ALL) can be preceded by a prodromal phase of bone marrow failure. In serial trephine biopsies in a girl with acquired bone marrow hypoplasia, we have identified a monoclonal B-cell precursor population characterized by a clone-specific IgH-FR3 gene rearrangement. Progression to ALL more than 4 months later was accompanied by acquisition of an additional T-cell receptor rearrangement. Thus, hypoplastic pre- and overt leukemia share a common clonal origin. Prospective biobanking and extended molecular analysis can help to better understand the nature and sequence of genetic events during progression of a covert (pre)leukemic clone.

Details about the publication

JournalPediatric Blood and Cancer
Volume56
Issue2
Page range301-303
StatusPublished
Release year2011
Language in which the publication is writtenEnglish
DOI10.1002/pbc.22734
KeywordsGenes T-Cell Receptor; Female; Humans; Preleukemia; DNA Neoplasm; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Adolescent; Gene Rearrangement; Genes Immunoglobulin Heavy Chain; Genes T-Cell Receptor; Female; Humans; Preleukemia; DNA Neoplasm; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Adolescent; Gene Rearrangement; Genes Immunoglobulin Heavy Chain

Authors from the University of Münster

Linden, Tobias
University Children's Hospital - Department of Paediatric Haematology and Oncology (UKM PHO)
Rössig, Claudia
University Children's Hospital - Department of Paediatric Haematology and Oncology (UKM PHO)