• Title of article

    6q deletion discriminates Waldenstrِm macroglobulinemia from IgM monoclonal gammopathy of undetermined significance

  • Author/Authors

    Marta and Schop، نويسنده , , Roelandt F.J. and Van Wier، نويسنده , , Scott A. and Xu، نويسنده , , Ruifang and Ghobrial، نويسنده , , Irene and Ahmann، نويسنده , , Gregory J. and Greipp، نويسنده , , Philip R. and Kyle، نويسنده , , Robert A. and Dispenzieri، نويسنده , , Angela and Lacy، نويسنده , , Martha Q. and Rajkumar، نويسنده , , S. Vincent and Gertz، نويسنده , , Morie A. and Fonseca، نويسنده , , Rafael، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2006
  • Pages
    4
  • From page
    150
  • To page
    153
  • Abstract
    IgM monoclonal gammopathy of undetermined significance (IgM MGUS) and Waldenström macroglobulinemia (WM) are sometimes clinically difficult to distinguish. In our previous study, deletion of the long arm of chromosome 6 (6q) was found in about half of WM patients. To further clarify the area of minimal deletion at 6q (6q−) and to address the issue of whether 6q− occurs in IgM MGUS, 12 IgM MGUS and 38 WM patients were studied by fluorescence in situ hybridization using probes targeting different chromosomal segments of 6q. No 6q deletions were found in IgM MGUS samples. Of 38 successfully studied WM patients, 21 (55%) showed a deletion of 6q. The area of minimal deletion was between 6q23 and 6q24.3, but the deletion usually encompassed a large fragment of the 6q arm. These results indicate that 6q− can distinguish WM from IgM MGUS and is likely to be a secondary event.
  • Journal title
    Cancer Genetics and Cytogenetics
  • Serial Year
    2006
  • Journal title
    Cancer Genetics and Cytogenetics
  • Record number

    1827885