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Coexistent Rearrangements of c-MYC,BCL2, andBCL6 Genes in a Diffuse Large B-Cell Lymphoma
Authors:Chiyoko?Ueda  author-information"  >  author-information__contact u-icon-before"  >  mailto:kyotolsg@kuhp.kyoto-u.ac.jp"   title="  kyotolsg@kuhp.kyoto-u.ac.jp"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Momoko?Nishikori,Toshio?Kitawaki,Takashi?Uchiyama,Hitoshi?Ohno
Affiliation:Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan. kyotolsg@kuhp.kyoto-u.ac.jp
Abstract:We present a patient with stage III de novo diffuse large B-cell lymphoma. The lymphoma cells showed mature B-cell immunophenotype but lacked surface immunoglobulin (Ig) expression. Long-distance and long-distance inverse polymerase chain reaction assays to detect the oncogene/Ig gene rearrangement revealed that the cells carried 3 independent fusion genes, namely, c-MYC/Ig heavy chain gene (IgH), BCL2/IgH, and Ig lambda light chain gene/BCL6. Thus, the lymphoma cells concurrently carried t(8;14)(q24;q32), t(14;18)(q32;q21), and t(3;22)(q27;q11), which developed in association with class switching, V/D/J recombination, and somatic hypermutation, respectively. The lymphoma responded to chemoradiotherapy, and the patient has been well for 2 years, suggesting that multiple oncogene rearrangements may not necessarily be associated with poor clinical outcome.
Keywords:Diffuse large B-cell lymphoma  c-MYC  BCL2  BCL6  Long-distance PCR
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