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Original Contribution

Journal of Cosmetic Dermatology, 12, 204--209

Chemical peeling with trichloroacetic acid and lactic acid for


infraorbital dark circles
Charitomeni Vavouli, MD,1 Andreas Katsambas, MD, PhD,2 Stamatis Gregoriou, MD, PhD,3 Anca
Teodor, MD, PhD,4 Carmen Salavastru, MD, PhD,4 Adina Alexandru, MD, PhD,4 & George
Kontochristopoulos, MD, PhD1
1
2nd Dermatology Department, Andreas Sygros Hospital, Athens, Greece
2
Department of Dermatology, University of Athens, Andreas Sygros Hospital, Athens, Greece
3
Department of Dermatology, University of Athens, Attikon Hospital, Athens, Greece
4
Second Clinic of Dermatology, Colentina Hospital, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania

Summary Background Periorbital dark circles are relatively common, affecting individuals
regardless of age, sex, and race. Available treatment includes bleaching creams,
topical retinoid acid, chemical peels, laser therapy, autologous fat transplantation –
injectable fillers, surgery (blepharoplasty), and chemical peeling.
Objective To evaluate the efficacy of a combination of trichloroacetic TCA 3.75% and
lactic acid 15% on improving the periorbital hyperpigmentation.
Patients/Methods Thirty patients with periorbital dark circles and skin types II, III, or
IV were included in the study. Chemical peeling was performed every week for a
series of four treatments. The effect was photo-documented, and a patient’s and
physician’s global assessment was evaluated.
Results Almost all the patients showed significant esthetic improvement. Physicians
assessed a fair, good, or excellent improvement in 93.3% of the patients. Patient’s
global assessment rated a fair, good, or excellent response in 96.7% of the patients.
The procedure itself had only mild and temporary adverse effects, such as erythema,
edema, frosting, dryness, and telangiectasias. The effects of treatment remained for at
least 4–6 months in the majority of patients with appropriate sun protection.
Conclusion The combination of trichloroacetic TCA 3.75% and lactic acid 15%
showed encouraging results on improving periorbital hyperpigmentation.
Keywords: dark circles, infraorbital hyperpigmentation, chemical peeling, trichlo-
roacetic acid, lactic acid

a significant cosmetic concern especially for female


Introduction
patients.2 DC interfere with the face appearance, giving
Dark circles (DC) under the eyes are defined as bilat- the patient a tired, sad, or hung-over look.1 Hyper-
eral, round, homogenous pigment macules on the chromia of the orbital region can be subdivided into
infraorbital regions.1 The condition is relatively com- primary or idiopathic and secondary type which is
mon affecting individuals regardless of age, sex, and associated with systemic or local diseases of a known
race. It worsens with the aging process, and it can be cause.3 DC are caused by multiple etiologic factors that
include dermal melanin deposition (nevus of Ota),
Correspondence: S Gregoriou, 2nd Dermatology Department, Andreas familiar or ethnic tendency, specific anatomic formali-
Sygros Hospital, I. Dragoumi 5, Athens 16121, Greece. E-mail: ties, postinflammatory hyperpigmentation secondary to
stamgreg@yahoo.gr atopic or allergic contact dermatitis, periorbital edema,
Accepted for publication March 12, 2013 superficial location of vasculature and shadowing due

204 © 2013 Wiley Periodicals, Inc.


Chemical peeling for infraorbital dark circles . C Vavouli et al.

to skin laxity, tear trough depression, medications, affected region performed <6 months prior to the
systemic diseases, fatigue, smoking, excessive sun expo- beginning of the study. Other exclusion criteria were
sure, etc.1,2 Periorbital pigmentation in actuality can be pregnancy, nursing, allergy, hypersensitivity to the
a combination of the aforementioned factors.4 On the components, photosensitivity, and unrealistic expecta-
other hand, it has been suggested that cutaneous hyper- tion. Digital photographs were taken for every patient
chromia of the orbital region is not necessarily associ- at baseline and after the treatment. These photographs
ated with systemic diseases, as it also occurs in healthy were analyzed by three independent dermatologists.
individuals.5 Available treatments for DC include bleach- Before therapy, a severity index score was performed
ing creams,6–9 topical retinoid acid,10 chemical peels,11 for each patient. The intensity of periorbital hyperpig-
laser therapy,12–15 autologous fat transplantation – mentation was evaluated as mild, moderate, advanced,
injectable fillers,16–19 and surgery (blepharoplasty).20 or severe, based on the color of the orbital region as
None of the existing topical therapies for DC has been compared to the patient’s color according to the Fitzpa-
found to be entirely satisfactory. Chemical peeling is a trick scale (Table 1).
medical procedure which constitutes controlled skin Patient’s demographics and DC grading scale before
damage, promoting regeneration and rejuvenation of treatment are shown in Table 2. Seven subjects had
tissues. It can be classified into three basic categories mild, 11 had moderate, eight had advanced, and four
according to the histologic depth of injury, whether this had severe hyperpigmentation. The correlation of DC
is superficial (effecting the horny layer and the vital por- with some factors which worsen the degree of hyper-
tion of the epidermis down to the basal layer), medium chromia in patients appears in Table 3.
(which effects the papillary portion of the dermis), or Combination of peeling agents consisted of TCA in
deep (which can reach the reticular dermis).21 Chemical concentration 3.75% and LA 15%. It was performed
peels are widely used for depigmentation in combination using the basic guidelines for chemical peelings. A
with topical agents22,23 or as monotherapy. degreasing wipe moistened with an acidified hydro-
The study evaluates the efficacy and safety of a new alcoholic solution with citric acid was used to remove
superficial chemical peeling consisting of trichloroacetic any impurities and excess oil from the surface of the
acid (TCA) and lactic acid (LA) (Enerpeel EL, Tebitech- eyelids. The texture of the peel was in a gel formula-
General Topics Lungolago Zanardelli, 32—25087 Sal o tion. The device applicator was a rigid element cover
(BS) – Italy). This combination peel enhances the depth with a thin layer of spongy material which allowed the
without using high concentration of the agent. It does precise application of the gel, so as to reduce the risk
not have the potential adverse effects of scarring and of involuntary contact with the ocular conjunctiva to
permanent depigmentation. a minimum. The patients were also instructed to keep
their eyes closed during the application. They were
subjected to peeling every week for a series of four
Material and methods
treatments. Four layers of the peel were applied to each
Twenty-nine female and one male patient with an age infraorbital area in the same session. The first layer of
range 24–68 years (mean ~ 43) years with infraorbital the peel was applied starting from the area where
hyperpigmentation were included in the study. Patients
were all those presenting at the outpatient clinics of Table 1 DC classification according to the phototype
our hospital and willing to have their periorbital
hyperpigmentation treated during a one-month period. DC grading scale Subject’s phototype Color of the orbital region
All were adult Mediterranean patients with skin types
Mild II Golden
II, III, or IV. Thirteen patients reported a positive fam- III Fairly dark
ily history (43%). Eleven patients were not using sun- IV Dark
screen and 22 were not applying it on the periorbital Moderate II Fairly dark
region before the treatment. Two patients suffered also III Dark
IV Chocolate
from melasma. Prior consent was taken from each Advanced II Chocolate
patient after explanation of the procedure. A detailed III Very dark
history was taken, and in some cases, a clinical and IV Black
laboratory testing was performed. Individuals were Severe II Very dark
III Black
excluded from the study if they presented inflamma- IV Blue-black
tion, infectious, systemic diseases, or any other treat-
ment (dermabrasion, laser, radiation, surgery) on the DC, Dark circles.

© 2013 Wiley Periodicals, Inc. 205


Chemical peeling for infraorbital dark circles . C Vavouli et al.

Table 2 Patient’s demographics and DC grading scale before


(a)
treatment

No. of Gender/ DC grading scale


patients age(years) Phototype before treatment

1 F/24 III Moderate


2 F/30 II Moderate
3 F/33 II Mild
4 F/34 IV Moderate
5 F/35 II Moderate
6 F/36 II Mild
7 M/36 II Moderate
8 F/36 III Severe
9 F/37 III Moderate (b)
10 F/37 II Advanced
11 F/37 IV Moderate
12 F/39 II Moderate
13 F/39 II Advanced
14 F/39 III Moderate
15 F/39 III Severe
16 F/42 IV Advanced
17 F/42 IV Severe
18 F/44 III Mild
19 F/45 III Moderate
20 F/46 II Moderate
21 F/46 III Advanced Figure 1 Patient no 30. Infraorbital dark circles due to photoag-
22 F/47 III Mild ing. (a) Before treatment. (b) Improvement after peeling therapy.
23 F/49 III Mild
24 F/49 IV Advanced
25 F/50 III Advanced (a)
26 F/52 II Mild
27 F/54 II Mild
28 F/55 III Advanced
29 F/66 IV Severe
30 F/68 IV Advanced

DC, Dark circles.

Table 3 Factors worsening DC, incidence in the present study

No. of No. of
Adverse factors patients patients% (b)

Family history of DC 13 43
No use of sunscreen 11 36.7
No use of sunscreen on the eyelids 22 73.3
Smoking 10 33.3
Alcohol 8 26.6
No exercise 14 46.7

DC, Dark circles.

hyperpigmentation was more intense. The duration of


the 1st, 2nd, and penultimate layer ranged between 1 Figure 2 Patient no 13. (a) Before and (b) after peel. Marked
to 2 min and in the last layer, about 5 min. Total time improvement of dark circles.
for a single session was 8–11 min. The peel was neu-
tralized with a wipe moistened with 12% solution of All patients were instructed to avoid direct sunlight, to
arginine. Also, patients were advised to wash the apply a sunscreen (SPF 50+) before any sun exposure,
treated area with pure water after the neutralization. and to wear sunglasses (Figs 1–3).

206 © 2013 Wiley Periodicals, Inc.


Chemical peeling for infraorbital dark circles . C Vavouli et al.

Table 4 Results of TCA–LA peel for the treatment of DC


(a)

Poor Fair Good Excellent

Physician’s global assessments


No. of patients 2 11 12 5
No. of patients% 6.7 36.7 40.0 16.6
Patient’s global assessments
No. of patients 1 8 14 7
No. of patients% 3.3 26.7 46.7 23.3

DC, Dark circles; TCA, trichloroacetic acid; LA, lactic acid.

(b) Table 5 Patient’s satisfaction

Not satisfied Slightly satisfied Very satisfied

No. of patients 4 7 19
No. of patients% 13.3 23.3 63.3

Table 6 Patient’s global tolerance

Poor Fair Good Excellent

No. of patients None 7 9 14


Figure 3 Patient no 11. Mother (Fig. 1) and daughter with the No. of patients% 0.0 23.3 30.0 46.7
same problem of dark circles. (a) During the 2nd peel (b) After
2nd peel.
categories: very satisfied, slightly satisfied, and not satis-
fied. Patient’s satisfaction is shown in Table 5.
Results
Safety was assessed by evaluating tolerance and
Skin lightening was observed in most patients from the adverse events. Most patients (76.7%) described a good
first peel with further improvement thereafter (Figs. 1– to excellent tolerability (patient’s global tolerance;
3). Among the three observers who examined the pho- Table 6) with only some mild discomfort (tingling,
tographs of each patient before and after the treatment, itching, burning sensations, or pain) during the ther-
none of them classified the patients as “worse” after the apy. Other irritating reactions of the treatment were
treatment. Medical observers performed clinical assess- the presence of erythema in 26.6% of the individuals,
ments using the following grading scale: 0–25% edema (6.6%), frosting (10%), dryness (6.6%), and the
improvement (poor), 26–50% improvement (fair), revelation of pre-existing telangiectasias (10%).
51–75% improvement (good), 76–100% improvement (Table 7). The most common adverse effect was
(excellent). They indicated an excellent improvement in
16.6%, a good in 40,0%, a fair in 36.7% and a poor in Table 7 Adverse events during and after the treatment, incidence
in this study
6.6% of the cases. Furthermore, 23.3% of the patients
assessed the efficiency of the treatment as excellent, Adverse events No. of patients No. of patients%
46.7% as good, 26.7% as fair and 3.3% as poor. The
results of global assessment among physicians and Tingling 7 23.3
patients presented differences without statistical signifi- Itching 1 3.3
Burning 4 13.3
cance. Both the patient’s and physicians’ global assess-
Pain 2 6.6
ments after the treatment are demonstrated in Table 4. Erythema 8 26.0
Most patients (86.6%) were satisfied with the outcome. Dryness 2 6.6
They were interviewed about their level of satisfaction Edema 2 6.6
Frosting 3 10.0
with the clinical results after the treatment. The patient
Telangiectasias 3 10.0
was requested to estimate the clinical results (patient’s Postoperatively hyperpigmentation None 0.0
global assessment; Table 5) and select one of three

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Chemical peeling for infraorbital dark circles . C Vavouli et al.

redness followed by tingling sensations and burning. keratinocyte removal (thinning melanin), by inhibition
However, these were only temporary and did not of tyrosinase, and through thickening the epidermis
necessitate further treatment. The exfoliation was most and the dermis (less visible vasculare).
pronounced 24–48 h after the peel treatment. The Combination peels have many advantages: (i) They
three patients, who had presented frosting, were trea- allow us to exploit the different properties of each
ted with topical corticosteroids for a week. The other agent for optimal results, (ii) minimize the risk of com-
participants were not asked to use any other topical plications by using low concentration, (iii) accelerate
product before and after the sessions except sunscreen. tissue regeneration and the subsequent recovery time,
No hyper-or hypopigmentation or scarring was observed and (iv) broaden the range of applications of chemical
post-treatment. peeling methods.
With regard to complications that may appear dur-
ing, immediately after, or in the post phase, there does
Discussion
not seem to be a restrictive factor, probably, due to
There is no ideal treatment for DC. Little is published their transient nature.
in the literature regarding this subject. In the present Additionally, this chemical peel has the advantage of
study, 30 healthy individuals with DC under the eyes well-homogenizing effect, thus combining convenience
were treated with chemical peeling using a combina- and less expensive cost compared with other treat-
tion of two peeling agents (TCA, LA) at low concentra- ments, but the applications must be repeated after a
tions. According to the results of the study, this certain time interval. The effects of treatment lasted for
combined peel is probably effective in the reduction of at least 4–6 months in the majority of patients with
the pigmentation in DC. appropriate sun protection. Despite the many sessions,
TCA applied to the skin produces modifications in this treatment poses a reliable therapeutic method for
the epidermis and dispersion of melanin. It has been the treatment of DC that appears to be effective, safe,
used at different concentrations for superficial, med- and well tolerated, achieving patient and physician
ium, and deep chemical peeling. It produces coagula- satisfaction.
tion of skin proteins and destruction of the epidermis
and the upper dermis, followed by epidermal and der-
Acknowledgments
mal regeneration with new collagen deposition and
increase in epidermal and dermal volume. The depth of This work was supported by the European Commission
skin necrosis is directly proportional to the concentra- under the 7th Framework Programme 2007–2013
tion of the TCA. It is possible to reach the dermis using through the Sectoral Operational Programmes focus on
a low-concentration solution applied to an epidermis human resource development and human resources,
that has been more permeable. It may become a med- Contract no. 2007RO051PO001, Educational Program:
ium-depth peel depending on the number of layers POSDRU/63/3.2/5/318: International Training in
applied in the same session, the contact time, the num- Dermato-cosmetics for Romanian Medics.
ber of treatment sessions previously performed, the
time interval between one treatment session and
another, the patient’s genetic-ethnic characteristics,
References
phototype and skin type. Also, the skin of the infraor- 1 Freitag FM, Cestari TF. What causes dark circles under
bital eyelids is very thin (thickness of approximately the eyes? J Cosmet Dermatol 2007; 6: 211–5.
0.5 mm). 2 Roh MR, Chung KY. Infraorbital dark circles: definition,
LA is an alpha hydroxy acid (AHA), the mechanism causes, and treatment options. Dermatol Surg 2009; 35:
of action of which is similar to glycolic acid. It facili- 1163–71.
3 Cymbalista NC, Prado de Oliveira ZN. Treatment of idio-
tates dissociation of epidermal cells and promotes des-
pathic cutaneous hyperchromia of orbital region (ICHOR)
quamation, dispersion of melanin, and increase in the
with intense pulsed light. Dermatol Surg 2006; 32:
synthesis of collagen and glycosaminoglycans. In addi- 773–784.
tion, it has also been described as having a tyrosinase- 4 Elson ML, Nacht S. Treatment of periorbital hyperpigmen-
inhibiting action and has been used in the treatment tation with topical vitamin K/vitamin A. Cosmet Dermatol
of melasma.24,25 1999; 12: 32–4.
The skin-lightening effect and normalization of 5 Aguilera Diaz L. Pathology and genetics of bipalpebral
hyperpigmentation can, in part, be explained by the hyperpigmentation. Actas Dermosifiliogr 1971; 62:
removal of melanosomes as the results of induced 397–410.

208 © 2013 Wiley Periodicals, Inc.


Chemical peeling for infraorbital dark circles . C Vavouli et al.

6 Palumbo A, d‘Ischia M. Mechanism of inhibition of mela- 16 Roh MR, Kim TK, Chung KY. Treatment of infraorbital
nogenesis by hydroquinone. Biochim Biophys Acta 1991; dark circles by autologous fat transplantation: a pilot
1073: 85–90. study. B J Dermatol 2009; 160: 1022–5.
7 Prignano F, Ortonne JP, Buggiani G et al. Therapeutical 17 Lemperle G, Morhenn V, Charrier U. Human histology and
approaches in melasma. Dermatol Clin 2007; 25: persistence of various injectable filler substances for soft tis-
337–42. sue augmentation. Aesthet Plast Surg 2003; 27: 354–66.
8 Kligman AM, Willis J. A new formula for depigmenting 18 Stewart DB, Morganroth GS, Mooney MA et al. Manage-
human skin. Arch Dermatol 1975; 111: 40–8. ment of visible granulomas following periorbital injection
9 Rigopoulos D, Gregoriou S, Katsambas A. Hyperpigmen- of poly-L-lactic Acid. Opthal Plast Reconstr Surg 2007; 23:
tation and melasma. J Cosmet Dermatol. 2007; 6: 298–301.
195–202. 19 Kane MA. Treatment of tear trough deformity and lower
10 Romero C, Aberdam E, Larnier C et al. Retinoic acid as lid bowing with injectable hyaluronic acid. Aesthet Plast
modulator of UVB-induced melanocyte differentiation. Surg 2005; 29: 363–7.
Involvement of the melanogenic enzymes expression. 20 Barton FE Jr, Ha R, Awada M. Fat extrusion and septal
J Cell Sci 1994; 107: 1095–103. reset in patients with the tear trough triad; a critical
11 Zakopoulou N, Kontochristopoulos G. Superficial chemical appraisal. Plast Reconstr Surg 2004; 113: 2115–21.
peels. J Cosmet Dermatol 2006; 5: 246–53. 21 Khunger N. Standard guidelines of care for chemical
12 Momosawa A, Kurita M, Ozaki M et al. Combined therapy peels. Indian J Dermatol Venereol Leprol 2008; 74: S5–12.
using Q-switched ruby laser and bleaching treatment 22 Soloman MM, Ramadan SA, Bassiouny DA, Abdelmalek
with tretinoin and hydroquinone for periorbital skin M. Combined trichloroacetic acid peel and topical ascorbic
hyperpigmentationin Asians. Plast Reconstr Surg 2008; acid versus trichloroacetic acid peel alone in the treat-
121: 282–8. ment of melasma: a comparative study. J Cosmet Dermatol
13 Goldberg DJ. Full-face nonablative dermal remodeling 2007; 6: 89–94.
with a 1,320 nm Nd:YAG laser. Dermatol Surg 2000; 26: 23 Humphreys TR, Werth V, Dzubow L, Kligman A. Treat-
915–8. ment of photodamaged skin with trichloroacetic acid and
14 Khan MH, Sink RK, Manstein D et al. Intradermally topical tretinoin. J Am Acad Dermatol 1996; 34: 638–44.
focused infrared laser pulses: thermal effects at defined tis- 24 Usuki A, Ohashi A, Sato H et al. The inhibitory effect of
sue depths. Laser Surg Med 2005; 36: 270–80. glycolic acid and lactic acid on melanin synthesis in mel-
15 Manstein D, Herron GS, Sink RK et al. Fractional photo- anoma cells. Exp Dermatol 2003; 12: 43–50.
thermolysis: a new concept for cutaneous remodeling 25 Sharquie KE, AI-Tikreety MM, AI-Mashhadani SA. Lactic
using microscopic patterns of thermal injury. Lasers Surg acid as a new therapeutic peeling agent in melasma.
Med 2004; 34: 426–38. Dermatol Surg 2005; 31: 149–154.

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