Topical clobetasol propionate treatment and cutaneous adverse effects in patients with early-stage mycosis fungoides: an observational study.
Administration, Topical
Adult
Aged
Aged, 80 and over
Atrophy
/ chemically induced
Clobetasol
/ administration & dosage
Female
Glucocorticoids
/ administration & dosage
Humans
Hypopigmentation
/ chemically induced
Male
Middle Aged
Mycosis Fungoides
/ drug therapy
Prospective Studies
Skin
/ drug effects
Skin Cream
/ administration & dosage
Skin Neoplasms
/ drug therapy
Journal
Cutis
ISSN: 2326-6929
Titre abrégé: Cutis
Pays: United States
ID NLM: 0006440
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
entrez:
1
7
2020
pubmed:
1
7
2020
medline:
23
4
2021
Statut:
ppublish
Résumé
Topical superpotent class I corticosteroids (CSs) are highly effective in the treatment of early-stage mycosis fungoides (MF) and are readily available, easily applied, and have minor side effects compared to other topical therapeutic options. Because MF is a chronic disease, prolonged treatment is needed, raising the concern of CS-induced cutaneous adverse effects (AEs). In this observational study, we aimed to evaluate the risk for skin AEs of clobetasol propionate cream 0.05% in patients with early-stage MF. Thirteen consecutive patients with MF were treated with clobetasol propionate cream 0.05% once or twice daily as monotherapy and were followed for 4 to 17 months. One participant was lost to follow-up, and the remaining 12 participants responded to treatment with topical clobetasol propionate with minimal side effects. With proper education and monitoring, topical CSs are a safe and effective mainstay of treatment for patches and flat plaques in patients with early-stage localized MF.
Substances chimiques
Glucocorticoids
0
Clobetasol
ADN79D536H
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM