Differential expression of TOX by skin-infiltrating T cells in Sézary syndrome and erythrodermic dermatitis

J Cutan Pathol. 2015 Sep;42(9):604-9. doi: 10.1111/cup.12490. Epub 2015 May 6.

Abstract

Background: The histopathologic differentiation between Sézary syndrome (SS) and erythrodermic dermatitis may be extremely difficult. In this immunohistochemical study, it was investigated if thymocyte selection-associated high mobility group box protein (TOX) and C-MYC can be used as additional diagnostic markers to differentiate between SS and erythrodermic dermatitis.

Method: Paraffin-embedded skin biopsies from 15 SS patients and 17 erythrodermic dermatitis patients were stained and scored for TOX or C-MYC expression.

Results: Strong nuclear staining for TOX in more than 50% of skin-infiltrating T cells was observed in 13 of 15 (87%) SS cases, whereas erythrodermic dermatitis cases showed weak nuclear staining in 11-50% (median: 25%) of the T cells; strong nuclear staining as found in SS was never observed in erythrodermic dermatitis. No significant differences in C-MYC expression between SS and erythrodermic dermatitis were found. In most patients of both groups, percentages of C-MYC positive-cells varied between less than 10 and 25% of skin-infiltrating T cells.

Conclusion: Our results suggest that strong expression of TOX in more than 50% of skin-infiltrating T cells in erythrodermic skin is a useful marker in the differentiation between SS and erythrodermic dermatitis, whereas staining for C-MYC does not contribute to differential diagnosis.

Keywords: C-MYC; Sézary syndrome; TOX; erythroderma; immunohistochemistry.

MeSH terms

  • Biopsy
  • DNA-Binding Proteins / metabolism
  • Dermatitis, Exfoliative / diagnosis
  • Dermatitis, Exfoliative / metabolism
  • Dermatitis, Exfoliative / pathology
  • Diagnosis, Differential
  • High Mobility Group Proteins / biosynthesis*
  • Humans
  • Immunohistochemistry
  • Sezary Syndrome / diagnosis
  • Sezary Syndrome / metabolism*
  • Sezary Syndrome / pathology*
  • Skin / pathology
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / pathology*
  • Transcription Factors / metabolism

Substances

  • DNA-Binding Proteins
  • High Mobility Group Proteins
  • MYCBP protein, human
  • TOX protein, human
  • Transcription Factors