Clinicopathological features of hepatosplenic T cell lymphoma: a single centre experience from India

Leuk Lymphoma. 2012 Apr;53(4):609-15. doi: 10.3109/10428194.2011.622421. Epub 2011 Dec 5.

Abstract

In a first series from India, we report 9 cases of hepatosplenic T cell lymphoma (HSTCL) seen in 23 months accounting for 4.2% of all mature T-non-Hodgkin lymphomas (NHLs) in our institution. All patients presented with organomegaly, cytopenias and had evidence of bone marrow involvement. The tumor cells had a blastic (55%) morphology with predominantly intrasinusoidal (33.3%) or intrasinusoidal with an additional interstitial component (33.3%). On flow cytometry, the classical phenotype (CD3+, CD7+, CD4-, CD8-, CD5-, CD56+/-) was seen only in 4 patients. Unusual variations included CD45 (overexpression), CD7 (dim expression), CD3 (overexpression, heterogeneous and dim), CD2 (overexpression), CD5 (heterogeneous), CD8 (heterogeneous or dim or overexpression) and aberrant expression of CD19. Fluoresvent in situ hybridisation (FISH) and karyotyping was abnormal in 5 out of 7 patients evaluated. All of the 5 cases showed abnormalities in chromosome 7 (ring chromosome or isochromosome 7q). Five patients died of disease and related complications in a span of 1-3 months after diagnosis whereas 4 were alive at their last follow up out of which 2 had documented a relapse. In our series, HSTCL was characterized by typical clinical and variable immunophenotypic features and a dismal clinical outcome.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Antigens, CD / metabolism
  • Chromosome Aberrations
  • Chromosomes, Human, Pair 7 / genetics
  • Fatal Outcome
  • Female
  • Flow Cytometry
  • Humans
  • Immunophenotyping
  • In Situ Hybridization, Fluorescence
  • India
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / pathology*
  • Lymphoma, T-Cell / genetics
  • Lymphoma, T-Cell / metabolism
  • Lymphoma, T-Cell / pathology*
  • Male
  • Middle Aged
  • Splenic Neoplasms / genetics
  • Splenic Neoplasms / metabolism
  • Splenic Neoplasms / pathology*
  • Young Adult

Substances

  • Antigens, CD