Mycosis fungoides exhibiting features of a dermatofibroma: a case report and review of the literature
Version of Record online: 8 NOV 2011
Copyright © 2011 John Wiley & Sons A/S
Journal of Cutaneous Pathology
Volume 39, Issue 1, pages 40–46, January 2012
How to Cite
Morcos, S. M., Girardi, M., Subtil, A., Wilson, L. D. and Cowper, S. E. (2012), Mycosis fungoides exhibiting features of a dermatofibroma: a case report and review of the literature. Journal of Cutaneous Pathology, 39: 40–46. doi: 10.1111/j.1600-0560.2011.01804.x
- Issue online: 27 DEC 2011
- Version of Record online: 8 NOV 2011
- Accepted for publication August 3, 2011
- cutaneous T-cell lymphoma;
- mycosis fungoides;
We present the case of a 60-year-old male with known stage IA mycosis fungoides (MF) who developed a suspicious tumor within a pre-existing lymphomatous plaque of the right forearm. Microscopy revealed an unusual mixed fibrohistiocytic proliferation as well as atypical intraepidermal and dermal lymphocytes. There was no evidence of large-cell transformation. Histopathological, immunohistochemical and clinical clues suggest this lesion might not have represented a dermatofibroma, but rather a hitherto unreported dermatofibroma-like process arising within a lesion of MF. The potential impact of this atypical lesion on the prognosis and clinical management of this patient highlights the importance of recognizing unusual clinical presentations of more common, benign lesions within this patient population.
Morcos SM, Girardi M, Subtil A, Wilson LD, Cowper SE. Mycosis fungoides exhibiting features of a dermatofibroma: a case report and review of the literature.