14q+ chromosome marker in a T-cell-rich B-cell lymphoma

J Pathol. 1996 Feb;178(2):227-31. doi: 10.1002/(SICI)1096-9896(199602)178:2<227::AID-PATH437>3.0.CO;2-9.

Abstract

Cytogenetic, in situ hybridization, and molecular studies were performed in a case of T-cell-rich B-cell lymphoma. Demonstration of Ig gene rearrangements for both heavy and light chains confirmed the B-lineage restriction of the neoplastic cell population. Moreover, as expected in B-cell malignancies, all abnormal karyotypes showed a 14q+ chromosome marker involving 14q32. The origin of the extra material on the derivative 14q+, as defined by chromosome painting with a library for chromosome 11, and Southern blotting for c-myc and bcl-2 rearrangements, remains unknown.

Publication types

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

MeSH terms

  • Blotting, Southern
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 14*
  • Female
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, B-Cell / immunology
  • Middle Aged
  • T-Lymphocytes / immunology*

Substances

  • Genetic Markers