Coexistence of BCL1/CCND1 and CMYC aberrations in blastoid mantle cell lymphoma: a rare finding associated with very poor outcome

Ann Hematol. 2004 Sep;83(9):578-83. doi: 10.1007/s00277-004-0879-2. Epub 2004 May 12.

Abstract

A patient with mantle cell lymphoma (MCL) of the pleomorphic blastoid subtype is reported. The disease was clinically aggressive and refractory to chemotherapy, and the patient survived only 2 months. Cytogenetically, a t(11;19;14)(q13;q13;q32) was found. Fluorescent in situ hybridization (FISH) and molecular analyses demonstrated involvement of the BCL1/CCND1 locus in a three-way translocation. In addition, subclonal abnormalities of the region 8q24 manifested either as a t(8;22)(q24;q11)/CMYC rearrangement or trisomy 8 were identified. The pathogenetic impact of this very uncommon association of BCL1/CCND1 and CMYC rearrangements in MCL is discussed and the literature is reviewed.

Publication types

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

MeSH terms

  • Aged
  • Chromosomes, Human / genetics
  • Cyclin D1 / genetics*
  • DNA, Neoplasm / genetics
  • Female
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Lymphoma, Mantle-Cell / genetics*
  • Lymphoma, Mantle-Cell / pathology*
  • Male
  • Middle Aged
  • Proto-Oncogene Proteins c-myc / genetics*
  • Translocation, Genetic / genetics*
  • Treatment Outcome
  • Trisomy / genetics*

Substances

  • DNA, Neoplasm
  • Proto-Oncogene Proteins c-myc
  • Cyclin D1