Treatment of Acquired Dermal Macular Hyperpigmentation With Oral Isotretinoin: A Multi-Institutional Retrospective Study of 121 Cases
Recommended Citation
Xu Z, Ding Y, Zhang C, Parsad D, Rodrigues M, Kumaran MS, Almutairi N, Hamzavi I, Amin J, Ghorbel HH, Xiang L, and Passeron T. Treatment of Acquired Dermal Macular Hyperpigmentation With Oral Isotretinoin: A Multi-Institutional Retrospective Study of 121 Cases. Pigment Cell Melanoma Res 2025;38(5):e70052.
Document Type
Article
Publication Date
9-1-2025
Publication Title
Pigment Cell Melanoma Res
Abstract
The term acquired dermal macular hyperpigmentation (ADMH) was introduced to unify Riehl's melanosis (RM), lichen planus pigmentosus (LPP), and related entities. These are cosmetically distressing pigmentary disorders that pose therapeutic challenges. To investigate the efficacy and safety of oral isotretinoin in treating ADMH, we conducted a muticenter retrospective study of patients with ADMH treated with oral isotretinoin between 2014 and 2024. Patients from Australia, China, Europe, India, Middle East, North America, and North Africa were included. Patients lost to follow-up before two visits were excluded. The response was graded by a 5-point Investigator's Global Assessment (IGA) scale. A total of 121 patients were included. Most patients (64.5%) were treated with a dose of 20 mg/d for an average of 8 months. Oral isotretinoin improved the severity of pigmentation in all RM and 85 (90.4%) LPP patients, with 17 (63.0%) RM and 31 (33.0%) LPP patients achieving marked improvement. RM patients responded better than LPP patients (p = 0.005). Patients with localized lesions (p = 0.0012), disease duration of less than 5 years (p = 0.046 for RM, p = 0.0272 for LPP), Fitzpatrick skin phototypes III-VI (p = 0.0081), or longer duration of treatment (p = 0.0178) responded better. Oral isotretinoin appears to be a promising treatment modality for ADMH.
Medical Subject Headings
Humans; Isotretinoin; Retrospective Studies; Female; Male; Administration, Oral; Hyperpigmentation; Adult; Middle Aged; Aged; Young Adult; Dermatologic Agents; Adolescent; Treatment Outcome
PubMed ID
40913266
Volume
38
Issue
5
First Page
70052
Last Page
70052
