Atypical fibroxanthoma: An unusual tumor

Matthias Thewes, Reinhard Engst, Tove Bye-Hansen, Jens Stodt, Wolf Ingo Worret, Johannes Ring

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

We report on an 84-year-old male patient with an erosive exophytic tumor on the helix of the left ear. Histologically, we found a striking dermal tumor with cellular pleomorphism. After immunohistochemical staining (positive for vimentin and negative for cytokeratin, smooth muscle-actin, desmin, melanoma-associated antigen, S-100) we diagnosed an atypical fibroxanthoma, which clinically has an excellent prognosis. We also found an immunoreactivity for the marker of invasion cathepsin pro-L and the suppressor gene p53. These findings may be helpful in the future for a better understanding of the pathogenesis and therapy of this tumor.

Original languageEnglish
Pages (from-to)187-188
Number of pages2
JournalEuropean Journal of Dermatology
Volume6
Issue number3
StatePublished - Apr 1996

Keywords

  • Atypical fibroxanthoma
  • Cathepsins
  • Immunohistochemistry
  • p53

Fingerprint

Dive into the research topics of 'Atypical fibroxanthoma: An unusual tumor'. Together they form a unique fingerprint.

Cite this