Clonal characteristics of cutaneous T cell lymphomas: cytogenetic evidence from blood, lymph nodes, and skin

J Invest Dermatol. 1982 Jan;78(1):69-75. doi: 10.1111/1523-1747.ep12497947.

Abstract

Chromosome studies were done on mitogen-stimulated lymphocytes from one or more tissues (blood, lymph nodes, skin lesions) in 15 patients with mycosis fungoides or Sézary syndrome. A cytogenetically abnormal clone was found in 10 individuals, including 6 with data from several tissues. In 4 cases the same aberrant clone was identified in a skin lesion as well as in blood and/or lymph node. The abnormal chromosome patterns ranged from hypodiploid to hypertetraploid, and there was no evidence of unrelated karyotypically-altered lines at different sites. A 6q- chromosome, previously reported in acute lymphocytic leukemia, was found in 2 patients. The results support the concept that cutaneous T cell lymphomas (CTCL) are clonal disorders, presumably unifocal in origin, with the skin lesions populated by cells from the same neoplastic clone that involves lymph nodes and blood.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Chromosome Aberrations*
  • Clone Cells / ultrastructure*
  • Female
  • Humans
  • Karyotyping
  • Lymph Nodes / ultrastructure
  • Lymphocytes / ultrastructure
  • Lymphoma / genetics*
  • Male
  • Middle Aged
  • Mycosis Fungoides / genetics
  • Sezary Syndrome / genetics
  • Skin / ultrastructure
  • Skin Neoplasms / genetics*
  • T-Lymphocytes*