Eruptive dermatofibromas and immunosuppression

Lorenzo Gualandri, Roberto Betti, Amilcare Cerri, Claudia Pazzini, Carlo Crosti

Research output: Contribution to journalArticle

Abstract

Dermatofibromas are benign tumours usually encountered in dermatology. Multiple and eruptive dermatofibromas are, on the contrary, unusual. Often the patients who show this peculiar cutaneous pattern are referred for immunosuppressive therapy or they have an immunosuppressive disease. We report the case of a woman affected by mycosis fungoides, who developed, in 2 months, 14 dermatofibromas on her legs. The personal history of the patient revealed a previous immunosuppressive treatment with systemic corticosteroids for interstitial pneumonia. Different etiological hypothesis have been proposed to explain the eruptive presence of multiple dermatofibromas and the alteration of the immune response, but the real mechanism is still unclear.

Original languageEnglish
Pages (from-to)45-47
Number of pages3
JournalEuropean Journal of Dermatology
Volume9
Issue number1
Publication statusPublished - 1999

Keywords

  • Dermatofibromas
  • Eruptive dermatofibroma
  • Immune response
  • Immunosuppression
  • Immunosuppressive therapy
  • Mycosis fungoides
  • Purple-red papules

ASJC Scopus subject areas

  • Dermatology

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  • Cite this

    Gualandri, L., Betti, R., Cerri, A., Pazzini, C., & Crosti, C. (1999). Eruptive dermatofibromas and immunosuppression. European Journal of Dermatology, 9(1), 45-47.