This protocol demonstrates a randomized split-face method for evaluating the efficacy and safety of Advanced Optimal Pulse Technology compared with standard Optimal Pulse Technology for treating erythromelanosis follicularis of faciei and colli.
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Method Article
* These authors contributed equally
This protocol demonstrates a randomized split-face method for evaluating the efficacy and safety of Advanced Optimal Pulse Technology compared with standard Optimal Pulse Technology for treating erythromelanosis follicularis of faciei and colli.
Erythromelanosis follicularis of faciei and colli (EFFC) is a chronic dermatological disorder characterized by hyperpigmentation, erythema, and follicular papules. Management remains challenging, as conventional treatments such as pulsed dye lasers can induce purpura and pose a risk of post-inflammatory hyperpigmentation, particularly in individuals with darker skin types. This article presents a standardized and reproducible clinical protocol using Advanced Optimal Pulse Technology (AOPT), a tunable intense pulsed light system, to target the vascular and pigmentary components of EFFC. A randomized, split-face clinical study involving 14 patients is described. Specific parameter settings, including dual-band vascular filters and adjustable pulse structures, were applied to the intervention side and compared with standard Optimal Pulse Technology (OPT) on the contralateral side. Quantitative assessments were performed using a skin colorimetric probe and a digital skin analysis imaging system to objectively evaluate lesion clearance. All 14 patients completed follow-up without attrition. The AOPT-treated side showed statistically significant reductions in erythema and melanin indices compared with the OPT control, with substantial inter-rater reproducibility for clinical evaluations. Additionally, the procedure was generally well tolerated, with few adverse events and limited downtime. Methodological limitations of this study include the small sample size, the absence of long-term follow-up (>6 months) to assess recurrence rates, and the lack of prospective clinical trial registration. This protocol provides clinicians with a standardized approach for applying AOPT to EFFC and may help address some limitations of traditional laser modalities in selected patients.
Erythromelanosis follicularis of faciei and colli (EFFC) is a distinct and persistent dermatological condition, particularly prevalent among young Asian males1,2,3. It is defined by well-demarcated erythema (telangiectasia), hyperpigmentation, and follicular papules, typically presenting symmetrically on the preauricular areas, cheeks, and lateral neck1,4. Although the etiopathogenesis is multifactorial, encompassing genetic predisposition and follicular keratinization abnormalities, the clinical impact can be substan....
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All methods described in this protocol were approved by the Medical Ethics Committee of Huashan Hospital (Approval No.: KY2017-004). Written informed consent was obtained from all participants before enrollment (Figure 1).
1. Patient selection and preparation
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Baseline characteristics
A total of 14 patients with clinically diagnosed erythromelanosis follicularis of faciei and colli (EFFC) were enrolled in this split-face study. The enrollment, allocation, and follow-up processes are detailed in the study flowchart (Figure 1). The cohort consisted of 12 males and 2 females, with ages ranging from 16 to 31 years (mean disease duration: 12.2 ± 3.83 years). Before treatment, there were no statistically sign.......
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EFFC remains a therapeutic challenge due to its multifactorial pathogenesis involving follicular hyperkeratosis, vascular dilation, and epidermal hyperpigmentation. While existing therapies such as topical keratolytics and pulsed dye laser (PDL) have demonstrated variable success, they are often constrained by limited efficacy or adverse effects, including purpura and PIH, particularly in Fitzpatrick skin types III–IV. In this randomized split-face study, AOPT showed greater clearance of both erythema and pigmentat.......
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The authors have no conflicts of interest to declare. AI-based tools were used only for language polishing and grammar correction during revision. No AI tools were used for data generation, statistical analysis, or scientific interpretation. The authors take full responsibility for the manuscript content.
| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| Anthelios Melt-in Milk Sunscreen (SPF 60) | La Roche-Posay | https://www.laroche-posay.com | Generic name used in text: broad-spectrum sunscreen |
| Aquasonic 100 Ultrasound Transmission Gel | Parker Laboratories, Inc. | 01-50 | Generic name used in text: ultrasound transmission gel |
| CeraVe Moisturizing Cream | L'Oréal (CeraVe) | https://www.cerave.com | Generic name used in text: gentle moisturizer |
| Cetaphil Gentle Skin Cleanser | Galderma Laboratories, L.P. | https://www.cetaphil.com | Generic name used in text: mild cleanser |
| GraphPad Prism (Version 9.0) | GraphPad Software, LLC | https://www.graphpad.com | Statistical analysis and graphing software |
| IBM SPSS Statistics (Version 26.0) | IBM Corp. | https://www.ibm.com/products/spss-statistics | Statistical analysis software |
| M22 Universal IPL System (AOPT and OPT Modules) | Lumenis Be Ltd. | https://lumenis.com/aesthetics/products/m22/ | Generic name used in text: intense pulsed light (IPL) system |
| Mexameter MX 18 | Courage + Khazaka Electronic GmbH | MX 18 | Generic name used in text: skin colorimetric probe |
| R (Version 4.1.2) | The R Foundation for Statistical Computing | https://www.r-project.org/ | Statistical computing environment |
| VISIA Complexion Analysis System (Generation 7) | Canfield Scientific, Inc. | VISIA-7 | Generic name used in text: skin analysis imaging system |