Febrile Ulceronecrotic Mucha-Habermann Disease: A Case Report and Review of the Literature

Authors

  • Eleni Sotiriou
  • Aikaterini Patsatsi
  • Christina Tsorova
  • Elisabeth Lazaridou
  • Dimitrios Sotiriadis

DOI:

https://doi.org/10.2340/00015555-0441

Keywords:

febrile ulceronecrotic Mucha-?abermann disease, pityriasis lichenoides and varioliformis acuta.

Abstract

Febrile ulceronecrotic Mucha-Habermann disease is a severe variant of pityriasis lichenoides et varioliformis acuta characterized by the sudden onset of ulceronecrotic skin lesions and associated with high fever and systemic symptoms. We report here a case of a 20-year-old woman in whom the disease started as pityriasis lichenoides et varioliformis acuta and evolved to febrile ulceronecrotic Mucha-Habermann disease. Almost 90% of the body surface was involved, together with high fever and malaise. Steroids alone proved to be an insufficient therapeutic procedure. The remission achieved was attributed to the use of methotrexate. To our knowledge, only 39 cases of febrile ulceronecrotic Mucha-Habermann disease have been reported in the literature to date.

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Published

2008-03-19

How to Cite

Sotiriou, E., Patsatsi, A., Tsorova, C., Lazaridou, E., & Sotiriadis, D. (2008). Febrile Ulceronecrotic Mucha-Habermann Disease: A Case Report and Review of the Literature. Acta Dermato-Venereologica, 88(4), 350–355. https://doi.org/10.2340/00015555-0441

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Section

Articles