Subcutaneous panniculitis-like T-cell lymphoma. Clinicopathologic, immunophenotypic, and genotypic analysis of alpha/beta and gamma/delta subtypes

  • Kevin E. Salhany
  • , William R. Macon
  • , John K. Choi
  • , Rosalie Elenitsas
  • , Stuart R. Lessin
  • , Raymond E. Felgar
  • , Darren M. Wilson
  • , Grzegorz K. Przybylski
  • , John Lister
  • , Mariusz A. Wasik
  • , Steven H. Swerdlow

Research output: Contribution to journalArticlepeer-review

327 Scopus citations

Abstract

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an uncommon cutaneous lymphoma that has been proposed as a distinct clinicopathologic entity, but studies of SPTCL are limited. We studied the clinicopathologic, immunophenotypic, and genetic features of 11 SPTCLs. All cases had a variable admixture of pleomorphic small, medium, or large lymphocytes and histiocytes infiltrating the subcutis in a Iobular panniculitislike pattern. A granulomatous reaction was seen in three cases and erythrophagocytosis in four. Karyorrhexis and fat necrosis were present in all cases. Angioinvasion was seen in seven SPTCLs; four had areas of coagulation necrosis. All cases expressed T-cell-associated antigens (CD3ε, CD45RO, or CD43) and T-cell receptors (TCR); nine expressed αβ TCRs and two expressed γδ TCRs. T- cell receptor-γ, TCRβ, or TCRδ genes were clonally rearranged in 8 of 10 cases studied. Both γδ SPTCLs expressed V(δ)2+ TCRs and were CD4-, CD8- and CD56+. CD56 was negative in seven of nine αβ SPTCLs and inconclusive in the other two. Six of nine αβ SPTCLs were CD8+; the CD4/CD8 phenotypes were indeterminate in the other three. Cytolytic granule-associated proteins were expressed by all SPTCLs (11 of 11 were TIA-1+, 4 of 4 were perforin+). In situ hybridization for Epstein-Barr virus-encoded RNA (EBER-1) was negative in all cases. Most patients responded to systemic chemotherapy or local radiation therapy. Seven patients are alive: four without disease (19- 73 months) and three with disease (32-72 months); four died: three of disease (3-25 months) and one without disease (42 months). We conclude that SPTCLs are clonal, EBV-, cytotoxic T-cell lymphomas derived from αβ T-cells or γδ T-cells. The γδ SPTCLs appear to be preferentially derived from the V(δ)2+ subset. Subcutaneous panniculitis-like T-cell lymphoma may be rapidly fatal or indolent; local therapy may be appropriate for some patients.

Original languageEnglish
Pages (from-to)881-893
Number of pages13
JournalAmerican Journal of Surgical Pathology
Volume22
Issue number7
DOIs
StatePublished - 1998

Keywords

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Antigens, CD/analysis
  • CD4-Positive T-Lymphocytes/immunology
  • CD8-Positive T-Lymphocytes/immunology
  • DNA, Neoplasm/analysis
  • Female
  • Gene Rearrangement, T-Lymphocyte/genetics
  • Genotype
  • Herpesvirus 4, Human/genetics
  • Humans
  • Immunoenzyme Techniques
  • Immunophenotyping
  • In Situ Hybridization
  • Lymphoma, T-Cell, Cutaneous/chemistry
  • Male
  • Middle Aged
  • Panniculitis/genetics
  • RNA, Viral/analysis
  • Receptors, Antigen, T-Cell, alpha-beta/analysis
  • Receptors, Antigen, T-Cell, gamma-delta/analysis
  • Skin Neoplasms/chemistry

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