Clonal evolution in atypical chronic granulocytic leukemia: A non-Philadelphia translocation

G. C. Bagby, B. Kaiser-McCaw, F. Hecht, R. D. Koler, J. W. Linman

    Research output: Contribution to journalArticlepeer-review

    8 Scopus citations

    Abstract

    Hemopoietic cells in chronic granulocytic leukemia (CGL) frequently contain a chromosome translocation involving chromosome 22 and another autosome, usually number 9. The translocated chromosome 22 is known as the Philadelphia (Ph) chromosome. The appearance of a second Ph chromosome is the most common cytogenetic abnormality in CGL signaling the blastic phase. For 6 yr we serially studied a man with atypical CGL whose marrow cells were marked by a translocation from chromosome 18 to chromosome 11 [46XY, t(11;18) (q23;q12)]. Three months prior to blast transformation there appeared an extra copy of the marker chromosome 18: 47XY,t(11;18) (q23;q12), + (18p11 →18q12). This man presents a new cytogenetic pattern of clonal evolution in CGL. The pattern is analogous to that of the Ph chromosome and is characterized by a balanced chromosomal rearrangement and the subsequent acquisition of an extra copy of the small translocation chromosome immediately prior to blast transformation.

    Original languageEnglish (US)
    Pages (from-to)997-1004
    Number of pages8
    JournalUnknown Journal
    Volume51
    Issue number6
    DOIs
    StatePublished - 1978

    ASJC Scopus subject areas

    • Biochemistry
    • Immunology
    • Hematology
    • Cell Biology

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