Management of bullous pemphigoid: The European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology

C. Feliciani, P. Joly, M. F. Jonkman, G. Zambruno, D. Zillikens, D. Ioannides, C. Kowalewski, H. Jedlickova, S. Kárpáti, B. Marinovic, D. Mimouni, S. Uzun, S. Yayli, M. Hertl, L. Borradori

Research output: Contribution to journalArticle

Abstract

Bullous pemphigoid is the most common autoimmune subepidermal blistering disease of the skin and mucous membranes. This disease typically affects the elderly and presents with itch and localized or generalized bullous lesions. In up to 20% of affected patients, bullae may be completely absent, and only excoriations, prurigo-like lesions, eczematous lesions, urticated lesions and/or infiltrated plaques are observed. The disease is significantly associated with neurological disorders. The morbidity of bullous pemphigoid and its impact on quality of life are significant. So far, a limited number of national treatment guidelines have been proposed, but no common European consensus has emerged. Our consensus for the treatment of bullous pemphigoid has been developed under the guidance of the European Dermatology Forum in collaboration with the European Academy of Dermatology and Venereology. It summarizes evidence-based and expert-based recommendations.

Original languageEnglish
Pages (from-to)867-877
Number of pages11
JournalBritish Journal of Dermatology
Volume172
Issue number4
DOIs
Publication statusPublished - Apr 1 2015

    Fingerprint

ASJC Scopus subject areas

  • Dermatology
  • Medicine(all)

Cite this

Feliciani, C., Joly, P., Jonkman, M. F., Zambruno, G., Zillikens, D., Ioannides, D., Kowalewski, C., Jedlickova, H., Kárpáti, S., Marinovic, B., Mimouni, D., Uzun, S., Yayli, S., Hertl, M., & Borradori, L. (2015). Management of bullous pemphigoid: The European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. British Journal of Dermatology, 172(4), 867-877. https://doi.org/10.1111/bjd.13717