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Erythema dyschromicum perstans is rather resistant to currently available treatments. It may persist unchanged for years although some cases eventually clear up by themselves. Treatments that may help improve the appearance of erythema dyschromicum perstans include: Topical steroids; Exposure to ultraviolet radiation
Na podstawie objawów klinicznych oraz obrazu histopatologicznego rozpoznano plamiste przebarwienia skóry typowe dla EDP (ashy dermatosis). Od roku zmiany skórne mają stacjonarny charakter, nie pojawiają się nowe plamy.
7 lip 2024 · Learn about ashy dermatosis AKA erythema dyschromicum perstans, its symptoms, underlying causes, and effective treatment options. Discover preventive measures to manage this skin condition and improve your overall skin health.
EDP is also known as dermatitis cenicienta (“ashy dermatosis”), los cenicientos (“the ashy ones”), and erythema chronicum figuratum melanodermicum, and pintoid. The pathogenesis is elusive, and often no etiologic cause can be assigned to the disease.
Suggested treatments for erythema dyschromicum perstans have included dapsone, clofazimine, corticosteroid and immunosuppressants without much evidence of efficacy. Idiopathic eruptive macular hyperpigmentation resolves spontaneously so does not usually require treatment.
Erythema dyschromicum perstans (also known as ashy dermatosis, and dermatosis cinecienta) is an uncommon skin condition with peak age of onset being young adults, but it may also be seen in children or adults of any age.
1 sty 2014 · Ashy dermatosis, also known as erythema dyschromicum perstans (EDP), is a rare dermatosis that was first described in El Salvador by Ramirez in 1957 [1]. It typically presents as asymptomatic, chronic, slowly progressive ashy-gray hyperpigmented macules on the trunk and proximal extremities.
