Next Article in Journal
Advances in 3D Printing Applications for Personalized Orthopedic Surgery: From Anatomical Modeling to Patient-Specific Implants
Previous Article in Journal
Endometriosis and Nutrition: Therapeutic Perspectives
Previous Article in Special Issue
Evaluating the Effects of Laser Treatments on Visible Changes in the Photoaging Process of the Skin Using Specialized Measuring Devices
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Treatment of Benign Pigmented Lesions Using Lasers: A Scoping Review

1
Department of Dermatology, Boston University School of Medicine, 609 Albany St., J502, Boston, MA 02118, USA
2
Dermatology Institute of Boston, Boston, MA 02118, USA
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2025, 14(11), 3985; https://doi.org/10.3390/jcm14113985
Submission received: 24 April 2025 / Revised: 3 June 2025 / Accepted: 3 June 2025 / Published: 5 June 2025
(This article belongs to the Special Issue Facial Plastic and Cosmetic Medicine)

Abstract

Lasers are widely employed in the treatment of melanocytic lesions. This scoping review evaluates 77 studies on the efficacy and safety of laser treatments for café-au-lait macules (CALMs), nevus of Ota (NOA), Becker’s nevus (BN), lichen planus pigmentosus (LPP), and other pigmented lesions. The Q-switched neodymium-doped yttrium aluminum garnet (Nd:YAG), particularly the 1064 nm, is the most frequently utilized laser, demonstrating strong efficacy for NOA and other dermal pigmentary disorders. Medium-wavelength lasers, including the Q-switched ruby and Alexandrite lasers, also show promise, though results vary based on lesion depth, skin type, and treatment protocols. Recurrence and adverse effects, including post-inflammatory hyperpigmentation (PIH) and hypopigmentation, are common, particularly in patients with darker skin tones. Future studies should standardize and optimize laser parameters across lesion types and skin tones, improve long-term efficacy, and prioritize inclusion of patients with diverse Fitzpatrick skin types to evaluate differential outcomes and promote equitable treatment efficacy.

1. Introduction

Lasers have emerged as an indispensable tool in dermatologic treatment, offering precision and versatility in managing a wide array of skin conditions, including melanocytic lesions [1]. Melanocytic lesions range from common conditions such as ephelides and lentigines to more complex entities like nevus of Ota and lichen planus pigmentosus [2]. The evolution of laser technologies has enabled clinicians to treat these lesions with greater specificity and minimal adverse side effects [2,3].
The application of lasers in melanocytic lesions works through selective photothermolysis, wherein pigment chromophores in skin absorb light at specific wavelengths, resulting in targeted destruction of melanin without damage to the surrounding tissue [4]. Selection of specific laser parameters such as wavelength, pulse width, and energy level allows for accurate targeting of specific chromophores, and use of the most appropriate laser for treatment [5]. Wavelength selectivity restricts absorption to affect only the targeted chromophore [5]. Laser pulse width is selected to be less than or equal to the target chromophore’s thermal relaxation time, to keep thermal damage limited to the undesired pigment. Laser energy levels are selected based on desired end point [5]. Commonly utilized lasers include the Q-switched lasers, such as the Q-switched neodymium-doped yttrium aluminum garnet (Nd:YAG), ruby lasers, and Alexandrite lasers, which are effective in treating dermal and epidermal pigmentary disorders [5]. IPL lasers are most effective in treating epidermal pigmented lesions, and fractional lasers use ablative and non-ablative resurfacing technology. Overall, response to laser treatment is influenced by a myriad of factors, necessitating a personalized approach [2,6].
While congenital melanocytic nevi are commonly treated with lasers, there is a paucity of data regarding efficacy across melanocytic lesions. Lesion such as nevus of Ota (NOA), lichen planus pigmentosus (LPP), Becker’s nevus (BN), and Hori’s nevus present unique therapeutic challenges due to the varying degrees of dermal and epidermal involvement [7,8,9,10]. The most common post-laser complications in the treatment of these pigmented lesions include post-inflammatory hyperpigmentation (PIH), hypopigmentation, and erythema; therefore, treatment efficacy must be carefully balanced against the risk of adverse effects [7,8,9,10]. Despite promising clinical outcomes reported in individual studies on lasers, the variance in treatment protocols, patient populations, and follow-up durations underscores the need for a comprehensive synthesis of the evidence.
This scoping review aims to evaluate the efficacy, periprocedural management, and side effect profiles of lasers in the treatment of melanocytic lesions, excluding congenital nevi. Congenital nevi were excluded from this study as they have a distinct pathophysiology. By systematically analyzing the available literature, we seek to identify patterns of clinical response, common adverse effects, and overall efficacy to provide clinicians with evidence-based guidance to optimize outcomes for patients with these complex, and often challenging, pigmentary disorders.

2. Materials and Methods

In accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, MEDLINE, EMBASE, and PubMed databases were systematically reviewed in December 2024 [11]. The following search phrases were utilized: “laser dermal melanosis”, “Becker’s nevi laser”, “nevi of Ota and Ito laser”, “speckled lentiginous nevi laser”, “nevus spilus laser”, “dermal melanocytosis laser”, and “segmental pigmentation disorder laser”. This search yielded 1717 articles. EMBASE was then searched with the same search criteria, and after duplicate records were removed, 325 additional articles were identified. Cochrane was then cross-referenced with the search criteria of “laser skin”, “laser melanin”, and “laser”. No additional articles were found through a cross reference of the Cochrane database. In total, 1768 articles were selected for further screening.
Initial exclusion criteria were applied, eliminating articles that lacked predetermined diagnoses, as well as case reports and epidemiologic studies. This resulted in 130 full articles. Each entry was then inputted into a shared Google Sheet, and PubMed IDs were utilized to identify papers when available; otherwise, the DOI or full citation was used. Authors A.D.Z. and M.L. reviewed the full text for all 130 articles and removed all articles with excluded diagnoses, non-human studies, and those where the full text was unavailable or not available in English. All records were reviewed by authors A.D.Z. and M.L., who cross-referenced selected articles to ensure data extraction was equivalent across individuals. After this analysis, there were 77 articles included (Figure 1) [12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87]. Successful clearance of lesions within a study was considered if 50% of patients or more reported clearance. An expanded analysis of café-au-lait macules (CALMs), nevus of Ota (NOA), Becker’s nevus (BN), and nevus spilus (NS) was undertaken due to the large proportion of assessed studies these diagnoses comprised, in order to better ascertain unique subgroup characteristics.

3. Results

3.1. Demographic Data of Included Studies

Studies were conducted most frequently on café-au-lait macules (35 studies), nevus of Ota and acquired bilateral nevus of Ota-like macules and Hori’s nevus (29), Becker’s nevus (20), nevus spilus (12), dermal melanocytosis (4), Rhiel’s melanosis (2), lichen planus pigmentosus (2), nevus of Ito (2), dermal melanocytosis (3), erythema dyschromia perstans (1), erythema follicularis faceie (1), and linear and whorled nevoid hypermelanosis (1). The number of enrolled lesions ranged from 4 to 620 and studies enrolled 42.82 patients on average. The age of patients enrolled ranged from 0 to 77 years. The Nd:YAG was the most studied laser (32 studies), followed by the Q-switched ruby (14) and the Q-switched Alexandrite laser (12). Of all the studies included, only two commented on the cost of treatment and patient opinion of cost. Furthermore, only 20 studies included data on patient preference of treatment.

3.2. Café-au-Lait Macules

Thirty-five studies were published on café-au-lait macules (CALMs) treated with lasers. There was an average of 50 patients enrolled in each study. Six studies included patients with Fitzpatrick skin type (FST) I, nine with FST II, thirteen with FST III, fifteen with FST IV, four with FST V, and two with FST VI. In twenty-three studies anesthetics were utilized, either topical or local, prior to laser treatment. The most commonly utilized lasers were the Nd:YAG (17 studies), Alexandrite PicoWay (6), and the Q-switched ruby (6). The average number of treatments for patients ranged from 1 session to 50. Twenty-one studies utilized aftercare, with nine treating patients with topical or antibiotics, two utilized steroids, and two utilized hydroquinone. The most frequently reported side effects in CALMs treated with lasers were hyperpigmentation (15 studies) and hypopigmentation (12) (Table 1).

3.3. Nevus of Ota, Acquired Bilateral Nevus of Ota-like Macules, Hori’s Nevus

Twenty-nine studies were published on nevus of Ota (NOA), acquired bilateral nevus of Ota-like macules (ABNOM), or Hori’s nevus. These were grouped for analysis as many studies did not distinguish between them. An average of 37 patients were enrolled in each study. FST I patients were involved in two studies, FST II in four, FST III in eleven, FST IV in sixteen, FST V in ten, and FST VI in four. Nineteen studies utilized topical or local anesthetic prior to treatment. The Nd:YAG was the most studied laser (12 studies), followed by the Q-switched ruby (9), and the PicoWay Alexandrite (7). On average, patients received 5.29 treatments. Fifteen studies utilized aftercare, with eight utilizing topical or oral antibiotics, four steroids, and one study utilized post-laser hydroquinone. The most reported side effects in NOA/ABNOM/Hori’s nevus treated with lasers were hyperpigmentation (13 studies) and erythema (10) (Table 2).

3.4. Becker’s Nevus

Twenty studies were conducted on the efficacy of lasers in the treatment of the melanocytic component of Becker’s nevus (BN). An average of 39 patients were enrolled in each study. Regarding FST: one study included patients with FST I, four with FST II, nine with FST III, ten with FST IV, four with FST V, and one with FST VI. Eleven studies utilized topical or local anesthetics prior to treatment. The Nd:YAG was the most studied (five studies) followed by intense pulsed light (IPL, 4). On average, patients received 2.42 treatments. Eleven studies utilized aftercare, with four utilizing topical or oral antibiotics, four utilizing steroids, and only two studies utilized post-laser hydroquinone. The most reported side effects in Becker’s nevus treated with laser were hyperpigmentation (nine studies), erythema (seven), and hypopigmentation (seven) (Table 3).

3.5. Nevus Spilus

There were twelve studies conducted on nevus spilus (NS). An average of 46 patients were enrolled. Of the studies who commented on FST, two included patients with FST I, three with FST II, four with FST III, four with FST IV, and one with FST V. Five studies utilized topical or local anesthetic prior to treatment. The Nd:YAG was the most studied laser (five studies) followed by the Alexandrite PicoWay (three). Six studies utilized aftercare, with three utilizing topical or oral antibiotics, two utilizing steroids, and two using post-laser hydroquinone. The most reported side effects in nevus spilus treated with laser were hyperpigmentation (five studies), hypopigmentation (four), erythema (four), and pain (four) (Table 4).

3.6. Other Lesions with Less than Five Studies

Three studies utilized lasers in the management of dermal melanocytosis. For dermal melanocytosis, the most commonly utilized lasers were the Nd:YAG (one study), Q-switched ruby (one), Q-switched Alexandrite (one), and Alexandrite PicoWay (one). The side effects noted in dermal melanocytosis were post-inflammatory hyperpigmentation (PIH), edema, erythema, and blistering. Two studies were conducted on the efficacy of laser treatment in Rhiel’s melanosis, with the Nd:YAG (one study) and fractional lasers (one) being the most studied lasers. Noted side effects were hyperpigmentation, erythema, and hypopigmentation. Two studies utilized lasers in the management of nevus of Ito which utilized the Q-switched ruby (one study), Nd:YAG (one), Q-switched Alexandrite (one), and the Alexandrite PicoWay (1). PIH, edema, and erythema were commonly reported side effects. Two studies were conducted on the efficacy of lasers on lichen planus pigmentosus (LPP), both of which utilized the Nd:YAG laser. The side effects noted were PIH, hyperpigmentation, erythema, and hypopigmentation. There was one study conducted on lasers in the management of erythema dyschromia perstans (EDP), one on erythromelanosis follicularis faciei (EFF), and one on linear and whorled nevoid hypermelanosis (LWNH).

4. Discussion

Melanocytic lesions can be challenging to treat with topical treatments. Medium-wavelength lasers that penetrate the dermis allow for the clearance of dermal pigment and improved overall efficacy. Across all studies, the Nd:YAG was the most frequently utilized laser in the treatment of benign pigmented lesions, specifically the 1064 nm wavelength one. The Nd:YAG can utilize two wavelengths, 532 nm for more superficial pigments and 1064 nm for deeper dermal pigments, as well as resurfacing and textural concerns. Within dermatology, the Nd:YAG is utilized for a myriad of problems ranging from hair removal to nail psoriasis and more [88,89]. Within the context of benign pigmented lesions, the Nd:YAG was successful in treating CALMs, NOA, ABNOM, Hori’s nevus, BN, and NS across a variety of FSTs. Most commonly, lesions were treated with a 3 mm spot size and a pulse duration of either 10 or 25 nanoseconds. Lasers were typically applied to intact skin without active infection, inflammation, or recent sun exposure, and patients were generally instructed to avoid photosensitizing agents prior to treatment. In addition, studies reported offering or utilizing anesthetic measures, such as topical lidocaine, cooling devices, or cryogen spray, to improve patient comfort during procedures. Fluence and number of sessions varied between studies, and only a minority clearly reported rationale for their selected parameters. While some lasers demonstrated a 100% success rate in the treatment of pigmented lesions, these findings should be interpreted with caution due to the limited number of studies. Small sample sizes increase the risk of overestimating efficacy, particularly in the absence of long-term follow-up or standardized outcome measures.
Café-au-lait macules (CALMs) are common hyperpigmented lesions that can vary greatly in size and degree of pigmentation. They were the most studied benign pigmented lesions, included in 35 studies. Most patients enrolled had FST of III or greater. In the treatment of CALMs, the most utilized lasers were the Nd:YAG, Alexandrite PicoWay, and the Q-switched ruby. Studies reported the successful use of all three lasers in the treatment of CALMs. Other meta-analysis on the treatment of lasers in CALMs have found that the Q-switched Nd:YAG is the most efficacious treatment, though they also note the use of other lasers such as the ruby laser and the Alexandrite laser [90,91]. Treatment of CALMs with lasers is well-studied, as one of the few effective treatment options. These lesions, while benign in nature, can significantly impact QoL. Therefore, if lesions are large or in a cosmetically sensitive location, they are often treated for overall cosmesis. The most reported side effects in CALMs were hyperpigmentation and hypopigmentation. Reported hyperpigmentation is likely in the setting of PIH due to the accumulation of melanin from the destruction of melanocytes in combination with inflammation-related increases in melanin production [92]. PIH is more commonly appreciated in more richly pigmented skin, such as that of FST III and above [93]. Therefore, it is not surprising that the given cohort with a higher proportion of patients with FST III and above commonly reported PIH and hyperpigmentation.
Nevus of Ota (NOA), acquired bilateral nevus of Ota-like macules (ABNOM), or Hori’s nevus (HN) were included in 29 studies. Many studies did not distinguish these diagnoses in their enrollment criteria. Therefore, for the sake of analysis, these were grouped into one category. NOA is a congenital dermal melanocytosis, typically unilateral, hypothesized to be caused by failure of melanocyte migration from the neural crest during embryogenesis, resulting in melanocytes trapped in the dermis most appreciated in the distribution of the trigeminal nerve [94]. ABNOM (also known as HN) are blue–brown macules occurring bilaterally on the upper portions of the face [95]. ABNOM is an acquired, bilateral condition thought to arise from the reactivation of dormant dermal melanocytes, potentially triggered by inflammation, skin aging, or an unknown cause [95]. HN is clinically similar to ABNOM but is often considered a distinct entity due to its later onset [10]. While these diagnoses are technically different, their treatment is very similar, and they are therefore often grouped together for analysis. Most patients enrolled with NOA, ABNOM, or HN had FST III or greater. Within this category, the most studied laser was again the Nd:YAG, followed by the Q-switched ruby and the Alexandrite PicoWay. Previously published reviews on the management of HN have outlined that laser treatment and dermabrasion are effective treatments in the management of this condition [10]. Similarly, NOA reviews have highlighted the efficacy of laser treatment in their management, especially with Q-switched lasers [7]. The most reported side effects were hyperpigmentation and erythema. As with CALMs, the hyperpigmentation is likely PIH in the setting of inflammation induced by the lasers. Additionally, erythema is a common side effect of nearly all laser treatments, especially appreciated in pulsed lasers, such as Q-switched lasers, due to epidermal immaturity and reduced melanin absorption of light [96].
Twenty studies were conducted on Becker’s nevus (BN), also known as Becker melanosis, with most studies enrolling patients with FSTs I through III. BN is a benign acquired hyperpigmentation with overlying hypertrichosis [97]. Due to the combination of hyperpigmentation and hypertrichosis, lasers are often utilized in the management of BN, which recent reviews have also highlighted [98]. This analysis, focusing solely on hyperpigmentation, found Nd:YAG to be the most studied laser, with the most common side effects being hyperpigmentation, erythema, and hypopigmentation.
There were twelve studies conducted on nevus spilus (NS), with most studies enrolling patients with FST I to III. Within the category of NS, there are many subtypes, but it generally presents as a hyperpigmented patch. An algorithm based on genetic and phenotypic patterns has been proposed for these subcategories [99]. While not applied in the studies reviewed, likely due to their publication before the algorithm was introduced, its inclusion in future studies could help elucidate if specific treatments are more efficacious for certain NS subtypes. The Nd:YAG was the most commonly studied treatment for NS, followed by the Alexandrite PicoWay. The most reported side effects of laser treatment for NS were hyperpigmentation, hypopigmentation, erythema, and pain.
While the search criteria included diagnoses such as dermal melanocytosis, Rhiel’s melanosis, nevus of Ito, lichen planus pigmentosus, erythema dyschromia perstans, erythromelanosis follicularis faciei, and linear and whorled nevoid hypermelanosis, there was a paucity of studies focusing on the utilization of lasers in their management. While these are rarer conditions, researchers should conduct additional studies to identify if preliminary success with laser management of these conditions can be replicated on a larger scale.

5. Conclusions

Within the realm of benign pigmented lesions, lasers are often a safe and efficacious choice for patients of all FSTs. However, a number of the studies did not report FST, which limits the generalizability of findings to diverse populations. FST is a critical determinant of laser–tissue interaction, particularly in relation to melanin content and the risk of pigmentary side effects. This omission underscores the need for more inclusive reporting standards to ensure that laser treatment recommendations are evidence-based and applicable to all skin types. Furthermore, we recommend that future studies not only include FST, but also utilize validated tools such as the Taylor Hyperpigmentation Scale and melanometers for objective measurements of skin pigmentation. Additionally, we acknowledge the potential for language bias introduced by the exclusion of non-English studies. Future reviews may benefit from multilingual search strategies or collaboration with translators to expand language inclusion criteria.
There is a paucity of data regarding cost of treatment and patient opinion on cost of laser treatment for pigmented lesions. Data regarding cost ought to also be published to identify treatments that are both efficacious and cost-effective for patients, especially as many lesions require multiple treatment sessions to reach partial or complete clearance. Despite the importance of affordability in treatment decision-making, only two studies in this review addressed cost. This omission is particularly relevant given that cosmetic laser treatments are often not reimbursed by insurance, potentially limiting access for many patients. Therefore, a thorough cost-effectiveness analyses ought to be included in future studies; not only for enhanced data on the subject matter, but also to ensure clinicians are able to counsel appropriately on cost-effectiveness of laser treatment for pigmented lesions.
Furthermore, patient preference ought to be studied concurrently to clinical clearance, as many patients may not seek full clinical clearance. Patient preference was inconsistently reported across studies, if reported at all. Future studies would benefit from a centralized patient preference reporting system, such as changes in the Dermatology Life Quality Index (DLQI) or the Patient Benefit Index (PBI), to elucidate the effect of these treatments not only on clinical clearance but also patient tolerability of these treatments. The addition of this data would be helpful in better understanding appropriate endpoints for the general patient population. Additionally, we did not differentiate whether “≥50% patient-reported clearance” was validated objectively (e.g., through clinician-rated photography) or subjectively via patient self-assessment, which may impact the reliability and comparability of reported outcomes across studies.

Author Contributions

Conceptualization, M.L. and N.A.V.; methodology, M.L. and A.D.Z.; investigation, A.D.Z., M.L. and J.C.; writing—original draft preparation, A.D.Z. and M.L.; writing—review and editing, A.D.Z., M.L., J.C. and N.A.V.; visualization, M.L. and J.C.; supervision, N.A.V. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
CALMsCafé-au-lait macules
NOANevus of Ota
BNBecker’s nevus
LPPLichen planus pigmentosus
Nd:YAGQ-switched neodymium-doped yttrium aluminum garnet
PIHPost-inflammatory hyperpigmentation
PRISMAPreferred Reporting Items for Systematic Reviews and Meta-Analyses
FSTFitzpatrick skin type
ABNOMAcquired bilateral nevus of Ota-like macules
IPLIntense pulsed light
NSNevus spilus
ECPErythema dyschromia perstans
EFFErythromelanosis follicularis faciei
LWNHLinear and whorled nevoid hypermelanosis
HNHori’s nevus
DLQIDermatology Life Quality Index
PBIPatient Benefit Index

References

  1. Goldberg, D.J. Laser treatment of pigmented lesions. Dermatol. Clin. 1997, 15, 397–407. [Google Scholar] [CrossRef] [PubMed]
  2. Araghi, F.; Ohadi, L.; Moravvej, H.; Amani, M.; Allameh, F.; Dadkhahfar, S. Laser treatment of benign melanocytic lesion: A Review. Lasers Med. Sci. 2022, 37, 3353–3362. [Google Scholar] [CrossRef] [PubMed]
  3. Alster, T.; Husain, Z. The role of lasers and intense pulsed light technology in dermatology. Clin. Cosmet. Investig. Dermatol. 2016, 9, 29–40. [Google Scholar] [CrossRef] [PubMed]
  4. Goldman, L.; Blaney, D.J.; Kindel, D.J.; Richfield, D.; Franke, E.K. Pathology of the effect of the laser beam on the skin. Nature 1963, 197, 912–914. [Google Scholar] [CrossRef]
  5. Ibrahimi, O.A.; Kilmer, S.L. Laser treatment of benign pigmented lesions. In Lasers and Energy Devices for the Skin; CRC Press: Boca Raton, FL, USA, 2013; pp. 57–73. [Google Scholar]
  6. Chan, H.H.; Kono, T. The use of lasers and intense pulsed light sources for the treatment of pigmentary lesions. Ski. Ther. Lett. 2004, 9, 5–7. [Google Scholar] [PubMed]
  7. Shah, V.V.; Bray, F.N.; Aldahan, A.S.; Mlacker, S.; Nouri, K. Lasers and nevus of Ota: A Comprehensive Review. Lasers Med. Sci. 2015, 31, 179–185. [Google Scholar] [CrossRef]
  8. Weston, G.; Payette, M. Update on Lichen Planus and its clinical variants. Int. J. Women’s Dermatol. 2015, 1, 140–149. [Google Scholar] [CrossRef]
  9. Dasegowda, S.; Basavaraj, G.; Nischal, K.; Swaroop, M.; Umashankar, N.; Swamy, S. Becker′s nevus syndrome. Indian J. Dermatol. 2014, 59, 421. [Google Scholar] [CrossRef]
  10. Kaur, H.; Sarma, P.; Kaur, S.; Kaur, H.; Prajapat, M.; Mahendiratta, S.; Kumar, S.; Thota, P.; Parsad, D.; Medhi, B. Therapeutic options for management of Hori’s nevus: A systematic review. Dermatol. Ther. 2019, 33, e13167. [Google Scholar] [CrossRef]
  11. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
  12. Trelles, M.A.; Verkruysse, W.; Pickering, J.W.; Vélez, M.; Sánchez, J.; Sala, P. Monoline argon laser (514 nm) treatment of benign pigmented lesions with long pulse lengths. J. Photochem. Photobiol. B 1992, 16, 357–365. [Google Scholar] [CrossRef] [PubMed]
  13. Nelson, J.S.; Applebaum, J. Treatment of superficial cutaneous pigmented lesions by melanin-specific selective photothermolysis using the Q-switched ruby laser. Ann. Plast. Surg. 1992, 29, 231–237. [Google Scholar] [CrossRef] [PubMed]
  14. Alster, T.S. Complete elimination of large café-au-lait birthmarks by the 510-nm pulsed dye laser. Plast. Reconstr. Surg. 1995, 96, 1660–1664. [Google Scholar] [CrossRef] [PubMed]
  15. Grossman, M.C.; Anderson, R.R.; Farinelli, W.; Flotte, T.J.; Grevelink, J.M. Treatment of cafe au lait macules with lasers. A clinicopathologic correlation. Arch. Dermatol. 1995, 131, 1416–1420. [Google Scholar] [CrossRef]
  16. Alster, T.S.; Williams, C.M. Treatment of nevus of Ota by the Q-switched alexandrite laser. Dermatol. Surg. 1995, 21, 592–596. [Google Scholar] [CrossRef]
  17. Tse, Y.; Levine, V.J.; McClain, S.A.; Ashinoff, R. The removal of cutaneous pigmented lesions with the Q-switched ruby laser and the Q-switched neodymium: Yttrium-aluminum-garnet laser. A comparative study. J. Dermatol. Surg. Oncol. 1994, 20, 795–800. [Google Scholar] [CrossRef]
  18. Watanabe, S.; Takahashi, H. Treatment of nevus of Ota with the Q-switched ruby laser. N. Engl. J. Med. 1994, 331, 1745–1750. [Google Scholar] [CrossRef]
  19. Kilmer, S.L.; Wheeland, R.G.; Goldberg, D.J.; Anderson, R.R. Treatment of epidermal pigmented lesions with the frequency-doubled Q-switched Nd:YAG laser. A controlled, single-impact, dose-response, multicenter trial. Arch. Dermatol. 1994, 130, 1515–1519. [Google Scholar] [CrossRef]
  20. Taylor, C.R.; Anderson, R.R. Treatment of benign pigmented epidermal lesions by Q-switched ruby laser. Int. J. Dermatol. 1993, 32, 908–912. [Google Scholar] [CrossRef]
  21. Taylor, C.R.; Flotte, T.J.; Gange, R.W.; Anderson, R.R. Treatment of nevus of Ota by Q-switched ruby laser. J. Am. Acad. Dermatol. 1994, 30, 743–751. [Google Scholar] [CrossRef]
  22. Fitzpatrick, R.E.; Goldman, M.P.; Ruiz-Esparza, J. Laser treatment of benign pigmented epidermal lesions using a 300 nsecond pulse and 510 nm wavelength. J. Dermatol. Surg. Oncol. 1993, 19, 341–347. [Google Scholar] [CrossRef] [PubMed]
  23. Grekin, R.C.; Shelton, R.M.; Geisse, J.K.; Frieden, I. 510-nm pigmented lesion dye laser. Its characteristics and clinical uses. J. Dermatol. Surg. Oncol. 1993, 19, 380–387. [Google Scholar] [CrossRef] [PubMed]
  24. Chang, C.J.; Nelson, J.S.; Achauer, B.M. Q-switched ruby laser treatment of oculodermal melanosis (nevus of Ota). Plast. Reconstr. Surg. 1996, 98, 784–790. [Google Scholar] [CrossRef]
  25. Somyos, K.; Boonchu, K.; Somsak, K.; Panadda, L.; Leopairut, J. Copper vapour laser treatment of café-au-lait macules. Br. J. Dermatol. 1996, 135, 964–968. [Google Scholar] [CrossRef] [PubMed]
  26. Shimbashi, T.; Kamide, R.; Hashimoto, T. Long-term follow-up in treatment of solar lentigo and café-au-lait macules with Q-switched ruby laser. Aesthetic Plast. Surg. 1997, 21, 445–448. [Google Scholar] [CrossRef]
  27. Hisano, A.; Kasai, K.; Fukuzumi, Y. An analysis of 114 patients with dermal melanocytosis on the trunk and extremities. Scand. J. Plast. Reconstr. Surg. Hand Surg. 1999, 33, 231–236. [Google Scholar] [CrossRef]
  28. Kunachak, S.; Leelaudomlipi, P. Q-switched Nd:YAG laser treatment for acquired bilateral nevus of ota-like maculae: A long-term follow-up. Lasers Surg. Med. 2000, 26, 376–379. [Google Scholar] [CrossRef]
  29. Moreno Arias, G.A.; Ferrando, J. Intense pulsed light for melanocytic lesions. Dermatol. Surg. 2001, 27, 397–400. [Google Scholar] [CrossRef]
  30. Levy, J.L.; Mordon, S.; Pizzi-Anselme, M. Treatment of individual café au lait macules with the Q-switched Nd:YAG: A clinicopathologic correlation. J. Cutan. Laser Ther. 1999, 1, 217–223. [Google Scholar] [CrossRef]
  31. Manuskiatti, W.; Sivayathorn, A.; Leelaudomlipi, P.; Fitzpatrick, R.E. Treatment of acquired bilateral nevus of Ota-like macules (Hori’s nevus) using a combination of scanned carbon dioxide laser followed by Q-switched ruby laser. J. Am. Acad. Dermatol. 2003, 48, 584–591. [Google Scholar] [CrossRef]
  32. Momosawa, A.; Yoshimura, K.; Uchida, G.; Sato, K.; Aiba, E.; Matsumoto, D.; Yamaoka, H.; Mihara, S.; Tsukamoto, K.; Harii, K.; et al. Combined therapy using Q-switched ruby laser and bleaching treatment with tretinoin and hydroquinone for acquired dermal melanocytosis. Dermatol. Surg. 2003, 29, 1001–1007. [Google Scholar] [CrossRef] [PubMed]
  33. Downs, A.M.; Rickard, A.; Palmer, J. Laser treatment of benign pigmented lesions in children: Effective long-term benefits of the Q-switched frequency-doubled Nd:YAG and long-pulsed alexandrite lasers. Pediatr. Dermatol. 2004, 21, 88–90. [Google Scholar] [CrossRef] [PubMed]
  34. Lee, B.; Kim, Y.C.; Kang, W.H.; Lee, E.S. Comparison of characteristics of acquired bilateral nevus of Ota-like macules and nevus of Ota according to therapeutic outcome. J. Korean Med. Sci. 2004, 19, 554–559. [Google Scholar] [CrossRef]
  35. Trelles, M.A.; Allones, I.; Moreno-Arias, G.A.; Vélez, M. Becker’s naevus: A comparative study between erbium: YAG and Q-switched neodymium:YAG; clinical and histopathological findings. Br. J. Dermatol. 2005, 152, 308–313. [Google Scholar] [CrossRef] [PubMed]
  36. Kagami, S.; Asahina, A.; Watanabe, R.; Mimura, Y.; Shirai, A.; Hattori, N.; Watanabe, T.; Tamaki, K. Treatment of 153 Japanese patients with Q-switched alexandrite laser. Lasers Med. Sci. 2007, 22, 159–163. [Google Scholar] [CrossRef]
  37. Choi, J.E.; Kim, J.W.; Seo, S.H.; Son, S.W.; Ahn, H.H.; Kye, Y.C. Treatment of Becker’s nevi with a long-pulse alexandrite laser. Dermatol. Surg. 2009, 35, 1105–1108. [Google Scholar] [CrossRef]
  38. Meesters, A.A.; Wind, B.S.; Kroon, M.W.; Wolkerstorfer, A.; van der Veen, J.W.; Nieuweboer-Krobotová, L.; van der Wal, A.C.; Bos, J.D.; Beek, J.F. Ablative fractional laser therapy as treatment for Becker nevus: A randomized controlled pilot study. J. Am. Acad. Dermatol. 2011, 65, 1173–1179. [Google Scholar] [CrossRef]
  39. Kroon, M.W.; Wind, B.S.; Meesters, A.A.; Wolkerstorfer, A.; van der Veen, J.P.W.; Bos, J.D.; Van der Wal, A.C.; Beek, J.F. Non-ablative 1550 nm fractional laser therapy not effective for erythema dyschromicum perstans and postinflammatory hyperpigmentation: A pilot study. J. Dermatol. Treat. 2012, 23, 339–344. [Google Scholar] [CrossRef]
  40. Wang, Y.; Qian, H.; Lu, Z. Treatment of café au lait macules in Chinese patients with a Q-switched 755-nm alexandrite laser. J. Dermatol. Treat. 2012, 23, 431–436. [Google Scholar] [CrossRef]
  41. Kar, H.; Gupta, L. Treatment of nevus spilus with Q switched Nd:YAG laser. Indian J. Dermatol. Venereol. Leprol. 2013, 79, 243–245. [Google Scholar] [CrossRef]
  42. Felton, S.J.; Al-Niaimi, F.; Ferguson, J.E.; Madan, V. Our perspective of the treatment of naevus of Ota with 1,064-, 755- and 532-nm wavelength lasers. Lasers Med. Sci. 2014, 29, 1745–1749. [Google Scholar] [CrossRef] [PubMed]
  43. Choi, C.W.; Kim, H.J.; Lee, H.J.; Kim, Y.H.; Kim, W.S. Treatment of nevus of Ota using low fluence Q-switched Nd:YAG laser. Int. J. Dermatol. 2014, 53, 861–865. [Google Scholar] [CrossRef]
  44. Wang, B.; Wu, Y.; Zhu, X.; Xu, X.G.; Chen, H.D.; Li, Y.H. An exploratory split-face study of a dual-wavelength laser system on erythromelanosis follicularis faciei in Chinese population. J. Eur. Acad. Dermatol. Venereol. 2014, 28, 1286–1291. [Google Scholar] [CrossRef] [PubMed]
  45. Sethuraman, G.; Sharma, V.K.; Sreenivas, V. Melanin Index in Assessing the Treatment Efficacy of 1064 nm Q Switched Nd-Yag Laser in Nevus of Ota. J. Cutan. Aesthet. Surg. 2013, 6, 189–193. [Google Scholar] [CrossRef] [PubMed]
  46. Piccolo, D.; Di Marcantonio, D.; Crisman, G.; Cannarozzo, G.; Sannino, M.; Chiricozzi, A.; Chimenti, S. Unconventional use of intense pulsed light. BioMed Res. Int. 2014, 2014, 618206. [Google Scholar] [CrossRef]
  47. Kim, H.-R.; Ha, J.-M.; Park, M.-S.; Lee, Y.; Seo, Y.-J.; Kim, C.-D.; Lee, J.-H.; Im, M. A low-fluence 1064-nm Q-switched neodymium-doped yttrium aluminium garnet laser for the treatment of café-au-lait macules. J. Am. Acad. Dermatol. 2015, 73, 477–483. [Google Scholar] [CrossRef]
  48. Chan, J.C.; Shek, S.Y.; Kono, T.; Yeung, C.K.; Chan, H.H. A retrospective analysis on the management of pigmented lesions using a picosecond 755-nm alexandrite laser in Asians. Lasers Surg. Med. 2016, 48, 23–29. [Google Scholar] [CrossRef]
  49. Levin, M.K.; Ng, E.; Bae, Y.S.; Brauer, J.A.; Geronemus, R.G. Treatment of pigmentary disorders in patients with skin of color with a novel 755 nm picosecond, Q-switched ruby, and Q-switched Nd:YAG nanosecond lasers: A retrospective photographic review. Lasers Surg. Med. 2016, 48, 181–187. [Google Scholar] [CrossRef]
  50. Miyamoto, H.; Takiwaki, H.; Yamano, M.; Ahsan, K.; Nakanishi, H. Color analysis of nevus of Ota for evaluation of treatment with a Q-switched alexandrite laser. Ski. Res. Technol. 1997, 3, 45–48. [Google Scholar] [CrossRef]
  51. Ouchi, T.; Ishii, K.; Nishikawa, T.; Ishiko, A. Acquired dermal melanocytosis of the face and extremities. Clin. Exp. Dermatol. 2016, 41, 643–647. [Google Scholar] [CrossRef]
  52. Balaraman, B.; Ravanfar-Jordan, P.; Friedman, P.M. Novel use of non-ablative fractional photothermolysis for café-au-lait macules in darker skin types. Lasers Surg. Med. 2017, 49, 84–87. [Google Scholar] [CrossRef] [PubMed]
  53. Ohshiro, T.; Ohshiro, T.; Sasaki, K.; Kishi, K. Picosecond pulse duration laser treatment for dermal melanocytosis in Asians: A retrospective review. Laser Ther. 2016, 25, 99–104. [Google Scholar] [CrossRef] [PubMed]
  54. Tang, M.; Cheng, Y.; Yang, C.; Liu, S.; Sheng, Y.; Li, Y.; Yin, W.; Zhou, W.; Yang, S.; Zhang, X. Nevus spilus: Treatment with fractional CO2 laser in combination with MedLite C6 laser: A preliminary study. Lasers Med. Sci. 2017, 32, 1659–1662. [Google Scholar] [CrossRef] [PubMed]
  55. Belkin, D.A.; Neckman, J.P.; Jeon, H.; Friedman, P.; Geronemus, R.G. Response to Laser Treatment of Café au Lait Macules Based on Morphologic Features. JAMA Dermatol. 2017, 153, 1158–1161. [Google Scholar] [CrossRef]
  56. Al-Saif, F.; Al-Mekhadab, E.; Al-Saif, H. Efficacy and safety of short-pulse erbium: Yttrium aluminum garnet laser treatment of Becker’s nevus in Saudi patients: A pilot study. Int. J. Health Sci. 2017, 11, 14–17. [Google Scholar]
  57. Artzi, O.; Mehrabi, J.N.; Koren, A.; Niv, R.; Lapidoth, M.; Levi, A. Picosecond 532-nm neodymium-doped yttrium aluminium garnet laser-a novel and promising modality for the treatment of café-au-lait macules. Lasers Med. Sci. 2018, 33, 693–697. [Google Scholar] [CrossRef]
  58. Belkin, D.A.; Jeon, H.; Weiss, E.; Brauer, J.A.; Geronemus, R.G. Successful and safe use of Q-switched lasers in the treatment of nevus of Ota in children with phototypes IV-VI. Lasers Surg. Med. 2018, 50, 56–60. [Google Scholar] [CrossRef]
  59. Alegre-Sanchez, A.; Jiménez-Gómez, N.; Moreno-Arrones, Ó.M.; Fonda-Pascual, P.; Pérez-García, B.; Jaén-Olasolo, P.; Boixeda, P. Treatment of flat and elevated pigmented disorders with a 755-nm alexandrite picosecond laser: Clinical and histological evaluation. Lasers Med. Sci. 2018, 33, 1827–1831. [Google Scholar] [CrossRef]
  60. Baek, J.O.; Park, I.; Lee, K.R.; Ryu, H.R.; Kim, J.; Lee, S.; Kim, Y.R.; Hur, H. High-fluence 1064-nm Q-Switched Nd:YAG laser: Safe and effective treatment of café-au-lait macules in Asian patients. J. Cosmet. Dermatol. 2018, 17, 380–384. [Google Scholar] [CrossRef]
  61. Kung, K.Y.; Shek, S.Y.; Yeung, C.K.; Chan, H.H. Evaluation of the safety and efficacy of the dual wavelength picosecond laser for the treatment of benign pigmented lesions in Asians. Lasers Surg. Med. 2019, 51, 14–22. [Google Scholar] [CrossRef]
  62. Lin, Y.; Liu, H.; Shi, W.; Wang, H.; Geng, J.; Guo, X.; Wang, J.; Zhang, F. Preliminary experience of the Q-switched 1064-nm neodymium:yttrium aluminum garnet laser in the treatment of Café-au-lait macules. J. Eur. Acad. Dermatol. Venereol. 2019, 33, e185–e186. [Google Scholar] [CrossRef] [PubMed]
  63. Zhang, B.; Chu, Y.; Xu, Z.; Sun, Y.; Li, L.; Han, X.; Wang, C.; Wei, L.; Liu, Y.; Ma, L. Treatment of Café-Au-Lait Spots Using Q-Switched Alexandrite Laser: Analysis of Clinical Characteristics of 471 Children in Mainland China. Lasers Surg. Med. 2019, 51, 694–700. [Google Scholar] [CrossRef] [PubMed]
  64. Alkhalifah, A.; Fransen, F.; Le Duff, F.; Lacour, J.P.; Wolkerstorfer, A.; Passeron, T. Laser treatment of epidermal nevi: A multicenter retrospective study with long-term follow-up. J. Am. Acad. Dermatol. 2020, 83, 1606–1615. [Google Scholar] [CrossRef] [PubMed]
  65. Wu, P.R.; Liu, L.J.; Zhang, Y.X.; Liu, Y.; Lin, X.X.; Ma, G. Intense pulsed light treatment for Becker’s nevus. J. Dermatol. Treat. 2021, 32, 334–339. [Google Scholar] [CrossRef]
  66. Gu, T.; Yuan, J.; Zhang, Y.; Li, Y.-H.; Wu, Y.; Gao, X.-H.; Chen, H.-D. A retrospective study of FQSRL and IPL in the treatment of Café-au-lait macule. J. Dermatol. Treat. 2021, 32, 544–547. [Google Scholar] [CrossRef]
  67. Bhari, N.; Sharma, V.K.; Singh, S.; Parihar, A.; Arava, S. Effect of Q-switched Nd-YAG laser on the clinical, pigmentary, and immunological markers in patients with lichen planus pigmentosus: A pilot study. Dermatol. Ther. 2020, 33, e13208. [Google Scholar] [CrossRef]
  68. Mehrabi, J.N.; Friedman, O.; Al-Niaimi, F.; Artzi, O. Retrospective photographic review of nontattoo indications treated by picosecond laser. J. Cosmet. Dermatol. 2020, 19, 612–621. [Google Scholar] [CrossRef]
  69. Zhong, Y.; Huang, L.; Chen, Y.; Yan, T.; Yang, B.; Man, M.Q. The efficacy of intense pulsed light for Becker’s nevus: A retrospective analysis of 45 cases. J. Cosmet. Dermatol. 2021, 20, 466–471. [Google Scholar] [CrossRef]
  70. Ungaksornpairote, C.; Manuskiatti, W.; Junsuwan, N.; Wanitphakdeedecha, R. A Prospective, Split-Face, Randomized Study Comparing Picosecond to Q-Switched Nd: YAG Laser for Treatment of Epidermal and Dermal Pigmented Lesions in Asians. Dermatol. Surg. 2020, 46, 1671–1675. [Google Scholar] [CrossRef]
  71. Zhong, Y.; Huang, L.; Chen, Y.; Yan, T.; Yang, B.; Man, M.Q. 755-nm Q-switched alexandrite laser does not markedly benefit Becker’s nevus: A retrospective analysis of 59 cases. Lasers Med. Sci. 2021, 36, 699–702. [Google Scholar] [CrossRef]
  72. Cen, Q.; Gu, Y.; Luo, L.; Shang, Y.; Rao, Y.; Zhu, J.; Han, Y.; Yu, W.; Liu, Y.; Wu, X.; et al. Comparative Effectiveness of 755-nm Picosecond Laser, 755- and 532-nm Nanosecond Lasers for Treatment of Café-au-Lait Macules (CALMs): A Randomized, Split-Lesion Clinical Trial. Lasers Surg. Med. 2021, 53, 435–442. [Google Scholar] [CrossRef] [PubMed]
  73. Kim, S.M.; Hwang, S.; Almurayshid, A.; Park, M.Y.; Oh, S.H. Non-Ablative 1927 nm Fractional Thulium Fiber Laser: New, Promising Treatment Modality for Riehl’s Melanosis. Lasers Surg. Med. 2021, 53, 640–646. [Google Scholar] [CrossRef] [PubMed]
  74. Zhuang, Y.; Huang, M.; Shen, J.; Wang, L.; Yang, L.; Jiang, A.; Yao, Z.; Yu, X. Comparison of the efficacy and safety between a low-fluence 1064-nm Q-switched neodymium-doped yttrium aluminum garnet laser and a conventional Q-switched 532-nm laser for the treatment of cafe-au-lait macules in 40 Chinese children: A prospective, randomized, parallel-controlled, evaluator-blinded trial. Lasers Med. Sci. 2022, 37, 279–286. [Google Scholar] [CrossRef] [PubMed]
  75. Al-Bakaa, M.K.; Al-Dhalimi, M.A.; Dube, P.; Khalaf, F.K. Evaluating the Roles of Different Types of Laser Therapy in Becker’s Nevus Treatment. J. Clin. Med. 2022, 11, 4230. [Google Scholar] [CrossRef]
  76. Cen, Q.; Zhu, J.; Zhou, L.; Yu, W.; Wu, X.; Liu, Y.; Ma, G.; Luo, L.; Lin, X. Comparison of the safety and efficacy of low fluence Q-switched 1064-nm and conventional Q-Switched 755-nm lasers in the treatment of café-au-lait macules: A prospective self-controlled trial. Lasers Surg. Med. 2022, 54, 1051–1059. [Google Scholar] [CrossRef]
  77. Kubicki, S.L.; Guo, E.L.; Richmond, H.; Friedman, P.M. Treatment of Nevus of Ota in Black patients with the 1064 nm QS or picosecond laser and nonablative fractional photothermolysis. Lasers Surg. Med. 2023, 55, 67–72. [Google Scholar] [CrossRef]
  78. Imagawa, K.; Kono, T.; Hanai, U.; Groff, W.F.; Komaba, C.; Tsunoda, Y.; Nemoto, H.; Akamatsu, T. Prospective comparison study of a 550 picosecond 755 nm laser vs a 50 ns 755 nm laser in the treatment of nevus of Ota. Lasers Med. Sci. 2023, 38, 55. [Google Scholar] [CrossRef]
  79. Alajlan, A.; Alsuwaidan, S. Efficacy of non-ablative 1927-nm fractional thulium fiber laser for the treatment of Becker’s nevus: Intra- and interobserver agreement study. Lasers Surg. Med. 2023, 55, 547–554. [Google Scholar] [CrossRef]
  80. Kim, Y.H.; Park, Y.J.; Baek, D.J.; Kwon, J.E.; Kang, H.Y. A novel treatment for Riehl’s melanosis targeting both dermal melanin and vessels. Photodermatol. Photoimmunol. Photomed. 2023, 39, 613–619. [Google Scholar] [CrossRef]
  81. Shin, J.-O.; Roh, D.; Shin, K.; Kim, H.-S.; Kim, B.-S.; Kim, M.-B.; Ko, H.-C. High-fluence 1064nm Q-switched Nd:YAG laser treatment for ectopic Mongolian spot. J. Dermatol. Treat. 2023, 34, 2255057. [Google Scholar] [CrossRef]
  82. Fernandez, J.K.; Guo, E.L.; Richmond, H.; Friedman, P.M. The 730 nm picosecond titanium sapphire laser for treatment of café-au-lait macules in all skin types. Lasers Surg. Med. 2024, 56, 257–262. [Google Scholar] [CrossRef] [PubMed]
  83. Swali, R.N.; Estupiñan, B.; Guo, E.L.; Richmond, H.; Friedman, P.M. Efficacy of 785-nm Picosecond Titanium Sapphire Laser for Treatment of Brown Nevus of Ota Lesions in FST II-V: A Retrospective Analysis. Dermatol. Surg. 2024, 50, 1046–1049. [Google Scholar] [CrossRef] [PubMed]
  84. Hur, H.; Baek, J.O.; Joo, J.S.; Jung, H.; Kim, Y.R.; Choi, S.J.; Shim, D.T. The treatment of infantile giant café au lait spot using golden parameter therapy with a high fluence 1064-nm Q-switched Nd: YAG laser. J. Dermatol. Treat. 2024, 35, 2390081. [Google Scholar] [CrossRef] [PubMed]
  85. Han, H.T.; Park, J.J.; Lee, J.S.; Lee, S.H. Nevus Spilus, Partial Unilateral Lentiginosis, and Linear and Whorled Nevoid Hypermelanosis: A Comparison of Clinical Features, Course, and Treatment Response. Acta Derm. Venereol. 2024, 104, adv40565. [Google Scholar] [CrossRef]
  86. Mhatre, M.A.; Malkud, S.; Mysore, V. Efficacy and safety of Q-switched Nd:YAG laser in the treatment of facial pigmentary lesions: A retrospective observational study. Iran. J. Dermatol. 2021, 24, 24–31. [Google Scholar] [CrossRef]
  87. Hamzah, M. The application of laser beam in various skin diseases. Med. J. Indones. 1995, 4, 105. [Google Scholar] [CrossRef]
  88. Sari, I.W.; Kurniawati, Y.; Diba, S. Comparison among Intense Pulsed Light, Alexandrite, and Long-Pulsed Neodymium-Doped Yttrium Aluminum Garnet 1064 Nm Lasers for Lower Leg Hair Removal: Case Series. Int. J. Trichology 2023, 15, 197–203. [Google Scholar] [CrossRef]
  89. Jaalouk, D.; Algarin, Y.A.; Pulumati, A.; Humeda, J.; Nouri, K. Lasers for the treatment of nail psoriasis: A systematic review. Int. J. Dermatol. 2024, 63, 1484–1494. [Google Scholar] [CrossRef]
  90. Guo, Z.-Z.; Wang, Z.-C.; Wang, D.; Ge, L.-L.; Li, Y.-H.; Gu, Y.-H.; Wang, W.; Wei, C.-J.; Gu, B.; Yao, M.; et al. Laser treatment for Cafe-au-lait Macules: A systematic review and meta-analysis. Eur. J. Med. Res. 2023, 28, 185. [Google Scholar] [CrossRef]
  91. Jha, S.K.; Mendez, M.D. Cafe Au Lait Macules. In StatPearls; StatPearls Publishing: Treasure Island, FL, USA, 2023. Available online: https://www.ncbi.nlm.nih.gov/books/NBK557492/ (accessed on 1 January 2025).
  92. Isedeh, P.; Kohli, I.; Al-Jamal, M.; Agbai, O.; Chaffins, M.; Devpura, S.; Mahan, M.; Vanderover, G.; Lim, H.; Matsui, M.; et al. An in vivo model for postinflammatory hyperpigmentation: An analysis of histological, spectroscopic, colorimetric and clinical traits. Br. J. Dermatol. 2016, 174, 862–868. [Google Scholar] [CrossRef]
  93. Prohaska, J.; Hohman, M.H. Laser Complications. In StatPearls; StatPearls Publishing: Treasure Island, FL, USA, 2023. Available online: https://www.ncbi.nlm.nih.gov/books/NBK532248/ (accessed on 1 January 2025).
  94. Agarwal, P.; Patel, B.C. Nevus of Ota and Ito. In StatPearls; StatPearls Publishing: Treasure Island, FL, USA, 2023. Available online: https://www.ncbi.nlm.nih.gov/books/NBK560574/ (accessed on 1 January 2025).
  95. Hori, Y.; Kawashima, M.; Oohara, K.; Kukita, A. Acquired, bilateral nevus of Ota-like macules. J. Am. Acad. Dermatol. 1984, 10, 961–964. [Google Scholar] [CrossRef] [PubMed]
  96. Trelles, M.A.; Mordon, S.; Svaasand, L.O.; Mellor, T.K.; Rigau, J.; Garcia, L. The origin and role of erythema after carbon dioxide laser resurfacing. A clinical and histological study. Dermatol. Surg. 1998, 24, 25–29. [Google Scholar] [CrossRef] [PubMed]
  97. Kaliyadan, F.; Ashique, K.T. Becker Melanosis. In StatPearls; StatPearls Publishing: Treasure Island, FL, USA, 2022. Available online: https://www.ncbi.nlm.nih.gov/books/NBK435999/ (accessed on 1 January 2025).
  98. Zhou, Y.J.; Zheng, D.L.; Hamblin, M.R.; Xu, Y.D.; Wen, X. An update on Becker’s nevus: Pathogenesis and treatment. Dermatol. Ther. 2022, 35, e15548. [Google Scholar] [CrossRef] [PubMed]
  99. Zhang, J.; Xu, Q.; Deng, D. Genetic and phenotypic diversities of nevus spilus phenotypes: Case series and a proposed diagnostic algorithm. Clin. Genet. 2023, 104, 593–597. [Google Scholar] [CrossRef]
Figure 1. PRISMA flowchart: outline of extracted data, presented as a PRISMA flowchart. * All records were reviewed by authors A.D.Z. and M.L. who cross-referenced selected articles to ensure data extraction was equivalent across individuals.
Figure 1. PRISMA flowchart: outline of extracted data, presented as a PRISMA flowchart. * All records were reviewed by authors A.D.Z. and M.L. who cross-referenced selected articles to ensure data extraction was equivalent across individuals.
Jcm 14 03985 g001
Table 1. Efficacy of laser treatment in café-au-lait macules (CALMs): efficacy of laser treatment alongside FST distribution and side effect profile.
Table 1. Efficacy of laser treatment in café-au-lait macules (CALMs): efficacy of laser treatment alongside FST distribution and side effect profile.
LaserN (%)FSTN (%)
Nd:YAG17 (48.57%)I6 (17.14%)
Successful15 (88.23%)II9 (25.71%)
Not Successful2 (11.76%)III13 (37.14%)
Q-Switched Ruby6 (17.14)IV15 (42.86%)
Successful6 (100%)V4 (11.43%)
Not Successful0 (0%)VI2 (5.71%)
Alexandrite PicoWay6 (17.14%)FST not Documented18 (51.43%)
Successful5 (83.33%)Side EffectsN (%)
Not Successful1 (16.67%)Hyperpigmentation15 (42.86%)
Q-Switched Alexandrite5 (14.29%)Hypopigmentation12 (34.43%)
Successful5 (100%)Erythema9 (25.71%)
Not Successful0 (0%)Crusting7 (20%)
PDL3 (8.57%)Scaring5 (14.29%)
Successful3 (100%)Pain5 (14.29%)
Not Successful0 (0%)Blistering5 (14.29%)
IPL2 (5.71%)Edema5 (14.29%)
Successful1 (50%)Depigmentation2 (5.71%)
Not Successful1 (50%)Uneven pigmentation2 (5.71%)
Copper Vapor1 (2.86%)Textural Changes1 (2.86%)
Successful1 (100%)Textural Changes1 (2.86%)
Not Successful0 (0%)
Erbium:YAG1 (2.86%)
Successful1 (100%)
Not Successful0 (0%)
Monoline Argon1 (2.86%)
Successful1 (100%)
Not Successful0 (0%)
Fractional1 (2.86%)
Successful1 (100%)
Not Successful0 (0%)
Note: Laser treatment was classified as successful if the study reported statistically significant improvement or if more than 50% of treated patients demonstrated clinical improvement.
Table 2. Efficacy of laser treatment in nevus of Ota (NOA), acquired bilateral nevus of Ota-like macules (ABNOM), or Hori’s nevus: efficacy of laser treatment alongside FST distribution and side effect profile.
Table 2. Efficacy of laser treatment in nevus of Ota (NOA), acquired bilateral nevus of Ota-like macules (ABNOM), or Hori’s nevus: efficacy of laser treatment alongside FST distribution and side effect profile.
LaserN (%)FSTN (%)
Nd:YAG12 (41.14%)I2 (6.90%)
Successful11 (91.67%)II4 (13.79%)
Not Successful1 (8.33%)III11 (37.93%)
Q-Switched Ruby9 (31.03%)IV16 (55.17%)
Successful8 (88.89%)V10 (34.48%)
Not Successful1 (11.11%)VI4 (13.79%)
Alexandrite PicoWay7 (24.14%)FST not Documented13 (44.83%)
Successful6 (85.57%)Side EffectsN (%)
Not Successful1 (14.29%)Hyperpigmentation13 (44.83%)
Q-Switched Alex6 (20.69%)Erythema10 (34.48%)
Successful6 (100%)Hypopigmentation9 (31.03%)
Not Successful0 (0%)Pain7 (24.14%)
CO21 (3.45%)Edema6 (20.69%)
Successful1 (100%)Crusting6 (20.69%)
Not Successful0 (0%)Depigmentation3 (10.34%)
Argon1 (3.45%)Blistering3 (10.34%)
Successful1 (100%)Petechiae3 (10.34%)
Not Successful0 (0%)Superficial erosions2 (6.90%)
Punctate Hemorrhage2 (6.90%)
Note: Laser treatment was classified as successful if the study reported statistically significant improvement or if more than 50% of treated patients demonstrated clinical improvement.
Table 3. Efficacy of laser treatment in Becker’s nevus (BN): efficacy of laser treatment alongside FST distribution and side effect profile.
Table 3. Efficacy of laser treatment in Becker’s nevus (BN): efficacy of laser treatment alongside FST distribution and side effect profile.
LaserN (%)FSTN (%)
Nd:YAG5 (25%)I1 (5%)
Successful5 (100%)II4 (20%)
Not Successful0 (0%)III9 (45%)
IPL4 (20%)IV10 (50%
Successful3 (75%)V4 (20%)
Not Successful1 (25%)VI1 (5%)
Q-Switched Alex3 (15%)FST not Documented9 (45%)
Successful1 (33.33%)Side EffectsN (%)
Not Successful2 (66.67%)Hyperpigmentation9 (45%)
Erbium:YAG3 (15%)Erythema9 (45%)
Successful3 (100%)Hypopigmentation7 (35%)
Not Successful0 (0%)Crusting4 (20%)
Q-Switched Ruby2 (10%)Scaring4 (20%)
Successful2 (100%)Blistering4 (20%)
Not Successful0 (0%)Pain3 (15%)
Long Pulse Alex2 (10%)Edema3 (15%)
Successful1 (50%)Textural changes3 (15%)
Not Successful1 (50%)Folliculitis1 (5%)
Alexandrite PicoWay2 (10%)Depigmentation1 (5%)
Successful2 (100)Uneven pigmentation1 (5%)
Not Successful0 (0%)
Thulium1 (5%)
Successful1 (100%)
Not Successful0 (0%)
Argon1 (5%)
Successful0 (0%)
Not Successful1 (100%)
Monoline Argon1 (5%)
Successful1 (100%)
Not Successful0 (0%)
Fractional1 (5%)
Successful1 (100%)
Not Successful0 (0%)
Note: Laser treatment was classified as successful if the study reported statistically significant improvement or if more than 50% of treated patients demonstrated clinical improvement.
Table 4. Efficacy of laser treatment in nevus spilus (NS): efficacy of laser treatment alongside FST distribution and side effect profile.
Table 4. Efficacy of laser treatment in nevus spilus (NS): efficacy of laser treatment alongside FST distribution and side effect profile.
LaserN (%)FSTN (%)
Nd:YAG5 (41.67%)I2 (16.67%)
Successful3 (60%)II3 (25%)
Not Successful2 (40%)III4 (33.33%)
Pico Alex3 (25%)IV4 (33.33%)
Successful3 (100%)V1 (8.33%)
Not Successful0 (0%)VI0 (0%)
Monoline Argon2 (16.67%)FST not Documented7 (58.33%)
Successful2 (100%)Side EffectsN (%)
Not Successful0 (0%)Hyperpigmentation5 (41.67%)
Q-Switched Ruby2 (16.67%)Hypopigmentation4 (33.33%)
Successful1 (50%)Erythema4 (33.33%)
Not Successful1 (50%)Pain4 (33.33%)
IPL2 (16.67%)Blistering3 (25%)
Successful2 (100%)Crusting3 (25%)
Not Successful0 (0%)Scaring2 (16.67%)
CO22 (16.67%)Depigmentation1 (8.33%)
Successful2 (100%)Uneven pigmentation1 (8.33%)
Not Successful0 (0%)Edema1 (8.33%)
Argon1 (8.33%)
Successful1 (100%)
Not Successful0 (0%)
Q-Switched Alex1 (8.33%)
Successful1 (100%)
Not Successful0 (0%)
Note: Laser treatment was classified as successful if the study reported statistically significant improvement or if more than 50% of treated patients demonstrated clinical improvement.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Zhang, A.D.; Clovie, J.; Lazar, M.; Vashi, N.A. Treatment of Benign Pigmented Lesions Using Lasers: A Scoping Review. J. Clin. Med. 2025, 14, 3985. https://doi.org/10.3390/jcm14113985

AMA Style

Zhang AD, Clovie J, Lazar M, Vashi NA. Treatment of Benign Pigmented Lesions Using Lasers: A Scoping Review. Journal of Clinical Medicine. 2025; 14(11):3985. https://doi.org/10.3390/jcm14113985

Chicago/Turabian Style

Zhang, Aurore D., Janelle Clovie, Michelle Lazar, and Neelam A. Vashi. 2025. "Treatment of Benign Pigmented Lesions Using Lasers: A Scoping Review" Journal of Clinical Medicine 14, no. 11: 3985. https://doi.org/10.3390/jcm14113985

APA Style

Zhang, A. D., Clovie, J., Lazar, M., & Vashi, N. A. (2025). Treatment of Benign Pigmented Lesions Using Lasers: A Scoping Review. Journal of Clinical Medicine, 14(11), 3985. https://doi.org/10.3390/jcm14113985

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop