Deletion 7q in B-cell low-grade lymphoid malignancies: a cytogenetic/fluorescence in situ hybridization and immunopathologic study

Cancer Genet Cytogenet. 1999 Feb;109(1):21-8. doi: 10.1016/s0165-4608(98)00139-3.

Abstract

Ten cases presenting a simple karyotype and del(7q) as a primary event were selected out of 353 patients referred as B-cell low-grade malignant lymphoproliferative disorders. Chromosome 7-specific painting probes confirmed the deletion that was tentatively assigned to bands q31q35. Chromosome 7 was involved in an interstitial deletion in seven cases, in an unbalanced translocation in two cases, and in a ring chromosome in one case. Common clinical/hematological features included advanced age, marked splenomegaly, and peripheral blood monoclonal IgM(D) lymphocytosis. Regardless of morphologic entity, most cases shared lymphoplasmacytoid features. Deletion 7q may delineate a variety of low-grade B-cell lymphoid disorders characterized by a common clinical history and immunopathologic similarities. The cytogenetic pattern and the ongoing work on molecular mapping of this deletion suggest that the loss of a putative tumor-supressor gene at 7q31q32 may constitute an early event in their pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Aged
  • Aged, 80 and over
  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosome Painting
  • Chromosomes, Human, Pair 7*
  • Cytogenetics / methods
  • Female
  • Humans
  • Immunoglobulin D / blood
  • Immunoglobulin M / blood
  • In Situ Hybridization, Fluorescence / methods
  • Lymphatic Metastasis
  • Lymphoma, B-Cell / genetics*
  • Lymphoma, B-Cell / immunology
  • Lymphoma, B-Cell / pathology*
  • Male
  • Middle Aged
  • Ring Chromosomes
  • Splenomegaly
  • Translocation, Genetic

Substances

  • Immunoglobulin D
  • Immunoglobulin M