Panniculitis-like T-cell-lymphoma in the mesentery associated with hemophagocytic syndrome: autopsy case report

Diagn Pathol. 2019 Jul 17;14(1):80. doi: 10.1186/s13000-019-0854-9.

Abstract

Background: Panniculitis-like T-cell lymphoma is an uncommon type of non-Hodgkin lymphoma, occurring usually in the form of nodules within the subcutaneous fat tissue of the extremities or trunk. In the literature, subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is described as a distinct type of T-cell lymphoma with a variable clinical behavior, depending on molecular phenotype of T-cell receptor (TCR) and on the presence or absence of hemophagocytic syndrome.

Case presentation: We present a bioptic and autoptic case of a 65-years old Caucasian man with panniculitic T-cell lymphoma with morphological and immunohistochemical features of SPTCL, limited to the retroperitoneal and mesenteric mass, i.e. without any cutaneous involvement, and associated with severe hemophagocytic lymphohistiocytosis.

Conclusion: A panniculitic T-cell lymphoma with morphological and molecular features of SPTCL, which is limited to mesentery, i.e. does not involve subcutaneous fat, seems to be exceedingly rare.

Keywords: Hemophagocytosis; Lymphohistiocytosis; Mesentery; Panniculitis; T-cell lymphoma.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Autopsy
  • Diagnosis, Differential
  • Humans
  • Lymphohistiocytosis, Hemophagocytic / diagnosis
  • Lymphohistiocytosis, Hemophagocytic / pathology*
  • Lymphoma, T-Cell / diagnosis
  • Lymphoma, T-Cell / pathology*
  • Lymphoma, T-Cell, Cutaneous / diagnosis
  • Lymphoma, T-Cell, Cutaneous / pathology
  • Male
  • Panniculitis / diagnosis
  • Panniculitis / pathology*
  • Skin Neoplasms / diagnosis
  • Skin Neoplasms / pathology
  • T-Lymphocytes / pathology*

Supplementary concepts

  • Subcutaneous panniculitis-like T-cell lymphoma