Consensus statement on the diagnosis and treatment of sclerosing diseases of the skin, Part 2: Scleromyxoedema and scleroedema.
Robert N A KnoblerMarija Geroldinger-SimićAlexander KreuterNicolas HunzelmannPia MoinzadehFranco RongiolettiChristopher P DentonLuc MouthonMaurizio CutoloVanessa SmithArmando GabrielliMartine BagotAnne B OlesenIvan FoeldvariAhmad JaliliVeli Matti KähäriSarolta KárpátiKristian KofoedMalgorzata OlszewskaJaana PaneliusPietro QuaglinoJulien SeneschalMichael SticherlingCord SunderkötterAdrian TanewPeter WolfMargitta WormAnna SkrokLidia RudnickaThomas KriegPublished in: Journal of the European Academy of Dermatology and Venereology : JEADV (2024)
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).