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Dermal morphological changes following salicylic acid peeling and microdermabrasion

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Background: Microdermabrasion and chemical peeling are popular, inexpensive, and safe methods for treatment of some skin disorders and to rejuvenate skin. Objectives: To study the alterations of the dermal connective tissue following salicylic acid peeling and microdermabrasion. Methods: Twenty patients were participated in our study. All participants underwent facial salicylic acid 30% peel or microdermabrasion (10 cases in each group) weekly for 6 weeks. Punch biopsies were obtained from the clinically normal skin of the right postauricular region 1 week before treatment (control group). Other punch skin biopsies were obtained 1 week after the end of the treatments from the left postauricular area. This region was treated in a similar way to the adjacent lesional skin (treated group). We used routine histological techniques (H&E stain), special stains (Masson trichrome and orcein stains), and image analyzer to study the alterations of the dermal connective tissues. Results: Our study demonstrates variations in the morphological changes between the control and the treated groups, and between chemical peels and microdermabrasion. Both salicylic acid 30% and microdermabrasion were associated with thickened epidermal layer, shallow dermal papillae, dense collagen, and elastic fibers. There was a significant increase among those treated sites vs control regarding epidermal thickness and collagen thickness. Also, there was a highly statistically significant increase among those treated with salicylic acid vs microdermabrasion regarding the epidermal, collagen, and elastin thickness. Conclusions: Both methods stimulate the repair process. The mechanisms underlying these variations are open for further investigations.
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Chapter
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Chemical peeling is a popular, relatively inexpensive, and generally safe method for treatment of some skin disorders and to refresh and rejuvenate skin. This article focuses on chemical peels and their use in routine clinical practice. Chemical peels are classified by the depth of action into superficial, medium, and deep peels. The depth of the peel is correlated with clinical changes, with the greatest change achieved by deep peels. However, the depth is also associated with longer healing times and the potential for complications. A wide variety of peels are available, utilizing various topical agents and concentrations, including a recent salicylic acid derivative, beta-lipohydroxy acid, which has properties that may expand the clinical use of peels. Superficial peels, penetrating only the epidermis, can be used to enhance treatment for a variety of conditions, including acne, melasma, dyschromias, photodamage, and actinic keratoses. Medium-depth peels, penetrating to the papillary dermis, may be used for dyschromia, multiple solar keratoses, superficial scars, and pigmentary disorders. Deep peels, affecting reticular dermis, may be used for severe photoaging, deep wrinkles, or scars. Peels can be combined with other in-office facial resurfacing techniques to optimize outcomes and enhance patient satisfaction and allow clinicians to tailor the treatment to individual patient needs. Successful outcomes are based on a careful patient selection as well as appropriate use of specific peeling agents. Used properly, the chemical peel has the potential to fill an important therapeutic need in the dermatologist's and plastic surgeon's armamentarium.
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To analyze the onset and extent of the dermatological changes associated with microdermabrasion. Eleven volunteers, aged 31-62 years old, underwent a series of six aluminum oxide microdermabrasion facial treatments spaced over 7 to 10-day intervals. White light photography and digital ultraviolet fluorescent photography and skin biopsies were obtained prior to the study, after three treatments, and after six treatments. A 90-day no-treatment period ensured, after which biopsies and photographs were taken. Clinical improvements in dyschromia, actinic changes and fine rhytides were observed after six treatments. Compared with the controls, the treated areas demonstrated the following histological changes: epidermal thickening with basal cell hyperplasia and mitotic activity; flattening and widening of the rete pegs; papillary dermal thickening with deposition of collagen and elastic fibers; and perivascular inflammation in the dermis. After the no-treatment period some of the clinical and histologic changes persisted although they were less than those present immediately after the last treatment. Serial ultraviolet photography following microdermabrasion treatments revealed changes in the skin's pigmentation pattern that correlated clinically with improvements in dyschromia. Clinical and histological changes are most likely secondary to a mechanism resembling a reparative process. The persistent changes after a period of no-treatment suggests that some of the changes could be permanent. Clinicians can use this data to better determine the optimal interval frequency and treatment intervals with microdermabrasion.