Analysis of hyperpigmentation and hypopigmentation after Er:YAG laser skin resurfacing

✍ Scribed by Yong Ju Kim; Ho-Sup Lee; Sang-Wook Son; Soo-Nam Kim; Young-Chul Kye

• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 233 KB
• Volume: 36
• Category: Article
• ISSN: 0196-8092
• DOI: 10.1002/lsm.20120

✦ Synopsis

Background and Objectives: Pigmentary disorderssuch as hyperpigmentation and hypopigmentation, are devastating complications of erbium:yttrium-aluminumgarnet (Er:YAG) laser resurfacing. This study was undertaken to assess the clinical and histopathologic features of hyperpigmentation and hypopigmentation following Er:YAG laser resurfacing, especially in darker skin. Study Design/Materials and Methods: One hundred and ninety patients (skin phototypes III and above), treated with Er:YAG lasers-short-pulsed and modulated (variable-pulsed and dual-mode) Er:YAG lasers-for skin resurfacing were recruited. The clinical features of hyperpigmentation and hypopigmentation were evaluated retrospectively using medical charts and serial photographs. For histopathologic examinations, skin biopsies were performed in three patients at hyperpigmentation sites and in four patients at hypopigmentation sites. Results: Hyperpigmentation was observed in 38.4% of the patients. Mean onset and duration were 3.5 and 7.2 weeks, and then it has faded away within 16 weeks in 93.2% of cases. Hypopigmentation was observed in 13.7% of the patients; its mean onset was 2 months after treatment, and it faded within 1 year in 85% of cases. The incidences and mean durations of these side effects were more intense and longer in patients treated with short-pulsed, variablepulsed, and dual-mode Er:YAG lasers, in increasing order. In terms of histopathologic examinations, melanin amounts in the epidermal basal layer were observed to vary. Conclusions: Hyperpigmentation and hypopigmentation are frequent complications of Er:YAG laser resurfacing. Long pulse duration-induced thermal damage seems to be the most important factor in terms of the induction of pigmentary disorders.