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 language | English |
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Pages (from-to) | 187-188 |
Number of pages | 2 |
Journal | European Journal of Dermatology |
Volume | 6 |
Issue number | 3 |
State | Published - Apr 1996 |
Keywords
- Atypical fibroxanthoma
- Cathepsins
- Immunohistochemistry
- p53