Exploring the potential of intradermal platelet‐rich plasma in treating acquired bilateral nevus of Ota‐like macule (Hori's nevus): A pilot study

医学 皮肤病科 黄褐斑 色素沉着 不利影响 富血小板血浆 水肿 太田痣 外科 内科学 黑色素瘤 血小板 癌症研究
作者
Pasinee Deeudomwongsa,Chumsaeng Chumsaengsri,Miguel Aristizabal,Chanisa Kiatsurayanon
出处
期刊:Journal of Cosmetic Dermatology [Wiley]
卷期号:23 (3): 803-811
标识
DOI:10.1111/jocd.16135
摘要

Abstract Background Hori's nevus is a common and challenging dermatological condition, often complicated by post‐inflammatory hyperpigmentation following treatment. Platelet‐rich plasma (PRP) has demonstrated efficacy in the treatment of hyperpigmentation disorders such as melasma and periorbital darkening. Given the benefits and minimally invasive nature of PRP treatments, exploring its application in managing Hori's nevus through further investigation is worthwhile. Aims To evaluate the safety and effectiveness of intradermal PRP therapy for the treatment of Hori's nevus. Methods Ten female patients received bilateral intradermal PRP injections every 2 weeks for a total of four treatments. The modified dermal pigmentation and severity index (mDPASI), mean melanin index (MI), brightening score, patient self‐assessment, and clinical photographs were evaluated at 2, 4, 8, and 12 weeks post‐treatment. Adverse events were also recorded to determine treatment safety. Results At 12 weeks post‐treatment, mDPASI decreased 38.86%, from 0.929 ± 0.617 to 0.568 ± 0.415 ( p < 0.05). The mean melanin index decreased 12.75%, from 208.650 ± 26.319 to 182.052 ± 17.028 ( p < 0.05). In addition, the mean brightness score evaluated by two experts was 1.4, indicating 25–50% improvement. At the end of the study, 50% of the patients reported 50–75% improvement. Side effects included pain, mild edema, and bruising, which resolved spontaneously within 3 days. No serious side effects were found. Conclusion Our results suggest that intradermal PRP therapy may be a safe and effective alternative for the treatment of Hori's nevus and can complement conventional interventions. However, further research with a larger sample size, control groups, and longer follow‐up is needed to confirm these findings.
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