2020
DOI: 10.1007/s10103-020-03008-z
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Clinical improvement of photoaging-associated facial hyperpigmentation in Korean skin with a picosecond 1064-nm neodymium-doped yttrium aluminum garnet laser

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Cited by 17 publications
(24 citation statements)
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“…Our observations in the present study are similar to previous studies using fractionated 755 [23] and 1064‐nm [22,40] picosecond lasers for the treatment of atrophic acne scars. These modalities were reported to also provide improvement [22] of postinflammatory erythema (PIE; Fig.…”
Section: Discussionsupporting
confidence: 92%
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“…Our observations in the present study are similar to previous studies using fractionated 755 [23] and 1064‐nm [22,40] picosecond lasers for the treatment of atrophic acne scars. These modalities were reported to also provide improvement [22] of postinflammatory erythema (PIE; Fig.…”
Section: Discussionsupporting
confidence: 92%
“…Mottled hypopigmentation or confetti‐like hypopigmentation is a permanent adverse effect reported in patients treated with low‐fluence 1064‐nm Q‐switched Nd:YAG laser toning [38,39]. Similar to the observation of a recent study in Koreans [40], our study likewise did not have any patients who developed punctate hypopigmentation after successive treatments with picosecond laser toning. Theoretically, a predominant photomechanical effect with a lesser degree of photothermal damage by picosecond laser application would reduce epidermal injury and non‐specific thermal damage to the neighboring structures [41,42].…”
Section: Discussionsupporting
confidence: 87%
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“…20 3 | RESULTS (Table 1). There were 2 RCTs, 22,23 3 single-arm trials, [24][25][26] and 3 case series, [27][28][29] for a total of 200 patients.…”
Section: Discussionmentioning
confidence: 99%
“…Human skin, unlike other organs, undergoes photoaging processes in addition to natural aging, which ultimately leads to aging-associated pigmentary changes. The acquired benign hyperpigmentation disorders associated with aging include a wide range of diseases such as lentigo, melasma, and post-inflammatory hyperpigmentation (PIH) [ 1 ]. Among them, senile lentigo is caused by a chronic exposure to ultraviolet radiation (UVR), resulting in a characteristic hyperpigmented basal epidermal layer [ 2 ].…”
Section: Introductionmentioning
confidence: 99%