Consensus statement on the diagnosis and treatment of sclerosing diseases of the skin, Part 2: Scleromyxoedema and scleroedema

Robert Knobler*, Marija Geroldinger-Simić, Alexander Kreuter, Nicolas Hunzelmann, Pia Moinzadeh, Franco Rongioletti, Christopher Denton, Luc Mouthon, Maurizio Cutolo, Vanessa Smith, Armando Gabrielli, Martine Bagot, Anne B. Olesen, Ivan Foeldvari, Ahmad Jalili, Veli Matti Kähäri, Sarolta Kárpáti, Kristian Kofoed, Malgorzata Olszewska, Jaana PaneliusPietro Quaglino, Julien Seneschal, Michael Sticherling, Cord Sunderkötter, Adrian Tanew, Peter Wolf, Margitta Worm, Anna Skrok, Lidia Rudnicka, Thomas Krieg

*Corresponding author for this work

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperReviewResearchpeer-review

Abstract

The term ‘sclerosing diseases of the skin’ comprises specific dermatological entities, which have fibrotic changes of the skin in common. These diseases mostly manifest in different clinical subtypes according to cutaneous and extracutaneous involvement and can sometimes be difficult to distinguish from each other. The present consensus provides an update to the 2017 European Dermatology Forum Guidelines, focusing on characteristic clinical and histopathological features, diagnostic scores and the serum autoantibodies most useful for differential diagnosis. In addition, updated strategies for the first- and advanced-line therapy of sclerosing skin diseases are addressed in detail. Part 2 of this consensus provides clinicians with an overview of the diagnosis and treatment of scleromyxoedema and scleroedema (of Buschke).

Original languageEnglish
JournalJournal of the European Academy of Dermatology and Venereology
Volume38
Issue7
Pages (from-to)1281-1299
Number of pages19
ISSN0926-9959
DOIs
Publication statusPublished - Jul 2024

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