A T-cell neoplasia showing clinicopathologic features of malignant histiocytosis with novel chromosomal abnormalities and N-ras mutation

Cancer. 1991 Apr 15;67(8):2103-10. doi: 10.1002/1097-0142(19910415)67:8<2103::aid-cncr2820670816>3.0.co;2-1.

Abstract

Malignant histiocytosis (MH) is a distinct disease entity defined clinically and morphologically. However, the neoplastic origin of MH is not well established. The authors report a 26-year-old woman who showed the typical clinicopathologic features of so-called MH. Cytogenetic and molecular genetic examinations were performed in addition to the morphologic and immunologic approach. The expression of CD2 and T-cell receptor gene rearrangements indicated the T-cell origin of this case. CD30, which is positive for anaplastic large cell lymphoma (Ki-1 lymphoma), was not expressed. The cytogenetic study revealed a clonal chromosome abnormality involving 3q25, 6p21, 11p15, and 11q21. An N-ras point mutation within codon 12 (GGT----GCT) was also detected. These finding indicate that MH defined clinically and morphologically is not a tumor of true histiocytic origin and that it should be reclassified on the basis of immunologic, cytogenetic, and molecular genetic data.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Bone Marrow / pathology
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • DNA, Neoplasm / analysis
  • Female
  • Gene Amplification
  • Genes, ras / genetics
  • Histiocytic Sarcoma / genetics*
  • Histiocytic Sarcoma / pathology*
  • Humans
  • Immunohistochemistry
  • Immunophenotyping
  • Liver / pathology
  • Mutation / genetics
  • Transformation, Genetic

Substances

  • DNA, Neoplasm