Trisomy 12 in Burkitt-like lymphoma associated with acquired immunodeficiency syndrome

Cancer Genet Cytogenet. 1987 Dec;29(2):245-51. doi: 10.1016/0165-4608(87)90235-4.

Abstract

Cytogenetic abnormalities have been reported in lymphoproliferative disorders, the most common of which is the t(8;14) translocation in Burkitt and Burkitt-like lymphomas. We report a 30-year-old homosexual male with Burkitt-like lymphoma and trisomy 12. This patient presented with persistent generalized lymphadenopathy and subsequently developed advanced lymphoma. Cell surface markers revealed a monoclonal pattern containing mu heavy chain and kappa light chain immunoglobulins. Cytogenetic analysis of bone marrow involved with lymphoma revealed an additional chromosome #12. Mitogen-stimulated cultures of peripheral blood showed a normal 46,XY karyotype. Trisomy 12 has been found in chronic lymphocytic leukemia and in other low-grade B-cell lymphoproliferative disorders, but not in Burkitt-like lymphoma.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acquired Immunodeficiency Syndrome / complications*
  • Adult
  • Bone Marrow / pathology
  • Burkitt Lymphoma / complications
  • Burkitt Lymphoma / genetics*
  • Burkitt Lymphoma / pathology
  • Chromosomes, Human, Pair 12*
  • Humans
  • Karyotyping
  • Male
  • Trisomy*