Author: Dr Ramez Barsoum, Resident Medical Officer, Princess Alexandra Hospital, Brisbane, QLD, Australia. DermNet Editor in Chief: Adjunct A/Prof Amanda Oakley, Dermatologist, Hamilton, New Zealand. Copy edited by Gus Mitchell/Maria McGivern. June 2019.
Skin of colour refers to non-white skin types, with a particular emphasis on Fitzpatrick skin phototypes V and VI. It is characterised by increased epidermalmelanin (a brown pigment), more widely distributed melanosomes (the melanin-containing granules within melanocytes), changing melanocyte response, and overactive fibroblasts.
Hyperpigmentation due to atopiceczema
Keloid scar
Discoid lupus erythematosus causing hypopigmentation and hyperpigmentation
How does skin of colour differ from white skin?
Since melanin absorbs and scatters the energy transmitted from ultraviolet radiation (UVR), persons with skin of colour experience less epidermal damage after exposure to UVR and show fewer signs of photoageing than people with lighter skin types [1,2].
Skin of colour almost always develops pigmentary changes when exposed to injury or inflammation (postinflammatory hyperpigmentation and postinflammatory hypopigmentation), whereas pigmentary changes are uncommon in white skin [3].
Melanin can act as a competitive chromophore (a coloured molecule that absorbs transmitted energy), which increases the risk of side effects after epidermal injury by a laser [4].
People with skin of colour have a higher prevalence of hypertrophic scarring and keloids after injury than those with white skin due to genetic factors associated with hyperactive fibroblasts [2,3].
What are the indications for laser therapy in skin of colour?
The medical indications for laser therapy are similar whatever the colour of the skin. However, women of colour often seek treatment for hyperpigmentation and uneven skin colour as these are common aesthetic concerns [2].
Its wavelength (1064 nm) is at the end of the absorption spectrum of melanin.
Nd:YAG laser results in sufficient thermal injury to dark coarse hairs and spares the epidermis [6].
It allows energy to be delivered slowly, resulting in heat dissipation and cooling, and minimising damage to the epidermis.
The use of the alexandrite laser (wavelength of 755 nm) has not been extensively studied in skin of colour. It has been reported to cause blistering in patients with Fitzpatrick skin types V and VI [7].
Use of a diode laser (wavelength 800 nm) has been reported to be mainly safe with low rates of complications, including the occurrence of transient blistering and pigment alteration [8].
Non-ablative Nd:YAG laser has fewer side effects compared to ablative laser resurfacing and produces comparable results.
Tattoo removal
Few studies on the removal of tattoos in skin of colour have been reported. Charcoal-based blue/black religious tattoos in Ethiopian patients with skin types V and VI have been removed using a Q-switchedNd:YAG [10]. In this study, almost half of the patients developed mild postinflammatory hyperpigmentation lasting between 2 and 4 months.
Removal of tattoos in skin of colour can be difficult and unpredictable because of the epidermal melanin, which absorbs the transmitted energy and prevents it from reaching the ink in the dermis.
What can help improve the outcomes of laser therapy in skin of colour?
Cooling
Cooling is used to protect the epidermis from thermal burn [11].
Contact cooling, which relies on conduction, can be active (eg, through the use of sapphire laser windows or copper tips) or passive (eg, through the use of ice cubes).
Non-contact cooling uses cold air convection or cryo-cooling.
Technique
Epidermal injury should be monitored carefully in skin of colour.
A Nd:YAG laser with a long wavelength and wider pulse times is often the most suitable device for use in skin of colour.
A test pulse or pulses can be used to check the immediate effects of the laser on the skin.
Multiple, short sessions can also help reduce epidermal damage compared to single or longer sessions [12].
Education
Patient expectations should be realistic, and they should be informed about the risk of complications and side effects associated with laser therapies [2].
References
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Grimes PE. Skin and hair cosmetic issues in women of color. Dermatol Clin 2000; 18: 659–65. DOI: 10.1016/s0733-8635(05)70217-5. PubMed
Szabo G, Gerald AB, Patnak MA, Fitzpatrick TB. Racial differences in the fate of melanosomes in human epidermis. Nature 1969; 222: 1081–2. DOI: 10.1038/2221081a0. PubMed
Kushikata N, Negishi K, Tezuka Y, Takeuchi K, Wakamatsu S. Non-ablative skin tightening with radiofrequency in Asian skin. Lasers Surg Med 2005; 36: 92–7. DOI: 10.1002/ism.20136. PubMed
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Grevelink JM, Duke D, van Leeuwen RL, Gonzalez E, DeCoste SD, Anderson RR. Laser treatment of tattoos in darkly pigmented patients: efficacy and side effects. J Am Acad Dermatol 1996; 34: 653–6. DOI: 10.1016/s0190-9622(96)80068-5. PubMed
Chiu CH, Chan HH, Ho WS, Yeung CK, Nelson JS. Prospective study of pulsed dye laser in conjunction with cryogen spray cooling for treatment of port wine stains in Chinese patients. Dermatol Surg 2003; 29: 909–15. DOI: 10.1046/j.1524-4725.2003.29255.x. PubMed
Adrian RM, Shay KP. 800 nanometer diode laser hair removal in African American patients: a clinical and histologic study. J Cutan Laser Ther 2000; 2: 183–90. DOI: 10.1080/146288300750163754. PubMed