Professional Documents
Culture Documents
Efficacy and Safety of 532 NM and 1064 nm.19
Efficacy and Safety of 532 NM and 1064 nm.19
net/publication/233942012
CITATIONS READS
11 1,290
4 authors:
Some of the authors of this publication are also working on these related projects:
All content following this page was uploaded by Muhsin Al-Dhalimi on 17 May 2016.
BACKGROUND Frictional dermal melanosis over bony prominences (Lifa disease) is a common pigmentary
skin disorder in Iraqi patients. Q-switched lasers are the gold standard treatment of correcting pigmentation;
among them are the 532-nm and 1,064-nm lasers.
OBJECTIVE To evaluate the efficacy of these lasers in the treatment of hyperpigmentation due to Lifa disease.
PATIENTS AND METHODS A prospective, comparative, controlled, split-lesion clinical trial study was
designed. Nineteen female patients with clinical diagnosis of Lifa disease were enrolled. Each patient was
treated for 3 sessions at 2-week intervals. A 532-nm Q-switched Nd:YAG laser was used on the left side and
1,064-nm on the right side of each lesion. Both objective and subjective parameters were assessed 1 and 3
months after the last treatment session. Darkness score, photographic assessment and patient satisfaction,
and improvement of itch were recorded, respectively.
RESULTS Seventeen patients completed the study. The color score changes of both sides demonstrated that
although both lasers were effective in reducing the pigmentation, the 1,064-nm wavelength had a more sig-
nificant response. Similar results were obtained for the photographic evaluations and patient satisfaction
scores. These changes were sustained throughout the 3 month follow-up.
CONCLUSION Both lasers were effective in the treatment of pigmentation abnormalities caused by Lifa
disease. However, the efficacy was greater with the 1,064-nm wavelength.
*Department of Dermatology, Faculty of Medicine, University of Kufa, Kufa, Iraq; †Department of Dermatology, Al-Sadir
Medical City, Najaf Health Directorate, Najaf, Iraq
· · ·
© 2014 by the American Society for Dermatologic Surgery, Inc. Published by Lippincott Williams & Wilkins
ISSN: 1076-0512 Dermatol Surg 2015;41:136–141 DOI: 10.1097/DSS.0000000000000238
·
136
Copyright © American Society for Dermatologic Surgery. Unauthorized reproduction of this article is prohibited.
AL-DHALIMI ET AL
pigmentation reduction of macular amyloidosis examination was performed for each patient to iden-
patches,15 a disease with many similarities to Lifa tify the lesion site(s), color, pigmentation pattern,
disease.6 distribution, lesion symmetry, and skin phototype.
Wood’s light (Waldmann Medizintechnik, Berlin,
Melanin absorbs and localizes the high-intensity irra- Germany) examination was completed for all patients
diation from Q-switched Nd:YAG laser leading to to assess the depth of pigmentation.
a rapid heating of melanosomes, thereby creating
a sharp temperature gradient between the melano- The treatment procedure was fully described to each
somes and the surrounding structures. This gradient patient, and informed consent was obtained from all
leads to thermal expansion, leading to generation and participants. Furthermore, this study was approved by
propagation of acoustic waves, which damage the the Ethical Scientific Committee of Dermatology and
melanosome-laden cells, thus the mechanism of action Venereology of the Iraqi Board for Medical
of Q-switched Nd:YAG laser is based on photo- Specializations.
thermal and photomechanical effects, resulting in
pigmentation reduction of the treated area. Use of this Nineteen female patients, aged 20 to 48 years, with
ultrashort pulsed laser can theoretically eliminate or disease duration ranging between 2 and 27 years were
reduce melanin in the upper dermis as demonstrated included. A 532-nm Q-switched Nd:YAG laser was
by histopathologic analyses.5–11 used on the left side and 1,064-nm on the right side of
each lesion. Symmetrical regions of the back measur-
Based on this therapeutic success, this study was ing approximately 10 · 5 cm2 were treated. The
designed to evaluate the efficacy and safety of 532-nm parameters of the laser used in this study were chosen
and 1,064-nm Q-switched Nd:YAG laser treatment of according to personal experience with treatment of
hyperpigmentation due to Lifa disease. pigmented lesions on the trunk with Q-switched Nd:
YAG using the same laser system (Ultralight Q-
switched Nd:YAG laser; Quanta System SPA, Milan,
Patients and Methods
Italy). These parameters were modified to achieve the
This is a prospective, comparative, clinical study per- blanching or whitening of the treated area, which
formed at the Laser Research Unit, College of Medi- represent the desired immediate response to laser
cine, University of Kufa, between October 2011 and treatment. Thus, in this study, the left side was treated
December 2012. with a Q-switched Nd:YAG 532-nm laser with the
following parameters: spot size, 3 mm and fluence,
Nineteen patients who were clinically diagnosed with 2.5 J/cm2 at a repetition rate of 5 Hz. The right side
frictional dermal melanosis over bony prominences was treated with the same laser type of 1,064-nm
(Lifa disease) were enrolled in this study. These wavelength with the following parameters: spot size,
patients did not receive any systemic or topical treat- 3 mm and fluence, 9 J/cm2 at the same repetition rate.
ment in the preceding 6 months. Exclusion criteria No local anesthetic was used during laser therapy,
were the presence of chronic systemic disease, personal and patients were questioned regarding the level of
history of hypertrophic scar and keloid formation, pain from the 2 of laser treatments by a visual analog
melanoma or other skin cancer, immunosuppression, scale (VAS) (0: no pain to 10: intolerable pain). At the
pregnancy, and lactation. end of each session, the treated sites were observed,
and the early skin reactions to the laser treatment
A full medical history was taken from each patient were recorded. Each patient was treated for 3 sessions
including name, age, sex, lesion site(s), age of onset at 2-week intervals.
and duration, presence and degree of itching, history
of friction (duration and agent), history of topical All participants were instructed to avoid any rubbing
medication, and family history and history of any or friction of skin with a washing agent (Lifa). The
associated skin or systemic diseases. Careful physical patients were also asked to avoid additional therapy
Copyright © American Society for Dermatologic Surgery. Unauthorized reproduction of this article is prohibited.
LASER TREATMENT OF FRICTIONAL DERMAL MELANOSIS
Photographic Assessment Two patients were defaulted from the study after the
Color photographs for each patient were taken in the first treatment session for unknown reasons, and the
same place with fixed illumination and distance at the remaining 17 patients completed the study. The baseline
baseline, before and after each therapy session and at color score was 3 (dark brown) for all patients before
each follow-up visit using a Sony digital, high sensi- initial treatment. The left side of the back was treated
tivity, 9.1 mega pixel, DSC-HX1 still camera. The with Q-switched Nd:YAG laser (532 nm), changing the
digital photographs were blindly assessed by 2 inde- color score to 2 (brown) in 11 (64.7%) patients, to 1
pendent dermatologists for the degree of pigmentation (light brown) in 3 (17.6%) patients, and no change in 3
improvement using a VAS from 0 to 10 (0: no pig- (17.6%) patients. On the right side of the back, which
mentation to 10: severe black pigmentation) before was treated with 1,064-nm laser, the change of color
treatment and at the end of follow-up period. score to 2 (brown) was achieved in 5 (29.4%) patients
Copyright © American Society for Dermatologic Surgery. Unauthorized reproduction of this article is prohibited.
AL-DHALIMI ET AL
TABLE 1. Mean 6 SD of Color Score and VAS Before and After Treatment With 532-nm and 1,046-nm Laser
and to 1 (light brown) in 12 (70.6%) patients. These by computer view of their digital photographs by 2
color score changes were statistically significant (p < independent dermatologists before treatment and at
.001; Table 1). The change of color score after treat- the end of follow-up period (Table 1). The change in
ment with the 1,064-nm laser was significantly greater the VAS score from the baseline for the region treated
compared with the 532-nm laser treatment (p < .027) with the 1,064-nm laser was statistically more sig-
(Figures 1 and 2). The improvement that was estab- nificant than the 532-nm laser treatment (p < .001).
lished after the last treatment session for both sides in Furthermore, patients were more satisfied with the
each patient was sustained without any obvious relapse 1,064-nm laser treatment compared with 532-nm
throughout the 3 months follow-up period. laser treatment (p < .006; Table 2).
The VAS from 0 to 10 was used to assess the degree of The itching disappeared after the first treatment ses-
pigmentation of both treated regions for each patient sion for all patients, independent of treatment type.
Figure 1. Patient with Lifa disease. (A) Before treatment. (B) Figure 2. Patient with Lifa disease. (A) Before treatment. (B)
After treatment—L: treated with 532-nm laser; R: treated After treatment—L: treated with 532-nm laser; R: treated
with 1,064-nm laser. with 1,064-nm laser.
Copyright © American Society for Dermatologic Surgery. Unauthorized reproduction of this article is prohibited.
LASER TREATMENT OF FRICTIONAL DERMAL MELANOSIS
TABLE 2. Patients Satisfaction After Treatment With 532-nm and 1,064-nm Lasers
Surprisingly, itching even ceased on the untreated melanosis,20 although it may be associated with high
sites. This effect persisted throughout the treatment risk for postinflammatory hyperpigmentation. In
sessions and the follow-up period. Recurrence of a recent study, a full-strength lactic acid (92%, pH 3.5)
itching was reported in 3 patients after the second was used as a chemical peeling agent in the treatment
treatment session. After laser treatment, burning sen- of this entity and was shown to be an effective and safe
sation and erythema persisted for 2 to 3 days for all option for the treatment of Lifa disease.12
patients. Generally, at the time of therapy, patients
believed that 532-nm laser was more painful than the Lasers have revolutionized the treatment of many
1,064-nm laser at the time of therapy (mean 6 SD, dermatological conditions, such as pigmentary dis-
6.7 6 1.0 for 532 nm and 4.3 6 0.9 for the 1,064 nm orders.21 Several types of lasers were developed specif-
based on a 1–10 analogical scale). Urticarial lesions ically for the treatment of pigmented skin lesions.22 The
disappeared after few hours. Petechiae lesions per- Q-switched Nd:YAG laser (1,064 nm and 532 nm) has
sisted for 5 to 7 days and then disappeared without yielded promising results in the treatment of many
any sequel. Desquamation was persisting for 1 to epidermal and dermal pigmented lesions.15,23
2 days.
Based on the positive results, the authors aimed to test
the efficacy of this type of laser therapy for the treat-
Discussion
ment of Lifa disease in Iraq. Both color score and
Frictional dermal melanosis over bony prominences objective assessment of patches reveal a positive effect
(Lifa disease) was described in many countries, includ- for both wavelengths of laser treatment for improved
ing Iraq. It was an extremely disfiguring pigmentary pigmentation. The degree of response was significant
disease, especially among females.3–11 Generally, dermal for both wavelengths but was more effective for the
hyperpigmentation was resistant to many therapeutic regions treated with the longer wavelength laser
interventions.13 The treatment of Lifa disease was often (Figure 1). The improvement was sustained without
challenging, especially when the patient continues to any obvious relapse throughout the follow-up period.
experience friction and Lifa usage.5 This malady has no These response rates were also accompanied by
satisfactory topical bleaching or peeling treatment, strong patient satisfaction scores. Moreover, no side
although if the patient stops the use of the Lifa or gains effects were observed, and the pain created by lasers
weight, the melanosis may disappear spontaneously at the time of treatment was tolerable.
over long time.10 However, many patients seek treat-
ment of this chronic and disfiguring disease. Additionally, itching subsided after first treatment
session in all patients who experienced itching ini-
Topical steroid and etretinate treatment have positive tially. This was true for either treatment type. Sur-
ameliorating effects,17–19 although the condition soon prisingly, this response was recorded in untreated
relapses after the etretinate is discontinued.19 Derm- regions as well. The exact mechanism behind this
abrasion could be a useful approach in dermal specific response is unclear and may be related to
Copyright © American Society for Dermatologic Surgery. Unauthorized reproduction of this article is prohibited.
AL-DHALIMI ET AL
psychological aspects or release of certain anti- 9. Kang HE, Rhee SH, Kim YC, Lee ES, Friction melanosis and striae distensae
caused by stretch training on a bench press. J Dermatol 2005;32:765–6.
inflammatory cytokines. The efficacy and safety of
10. Prabhakara VG, Chandra S, Krupa DS. Frictional pigmentary
therapy were not affected by the age of patients, dermatoses: a clinical and histopathological study of 27 cases. Indian J
duration of disease, or skin phototype of patients. Dermatol Venereol Leprol 1997;63:99–100.
11. Sharquie KE, Al-Dhalimi MA, Noaimi AA, Al-Sultany HA. Lifa disease:
frictional dermal melanosis over bony prominences (clinicopathological
All results of this study support the use of the 1,064- study). J Chem Dermatol Sci Appl 2012;2:196–200.
nm wavelength over 532-nm wavelength. This may be 12. Sharquie KE, Al-Dhalimi MA, Noaimi AA, Al-Sultany HA. Lactic acid
explained by the fact that melanin pigments may reach as a new therapeutic peeling agent in the treatment of lifa disease
(frictional dermal melanosis). Indian J Dermatol 2012;57:444–8.
deeper layers of the dermis,11 and the 1,064-nm laser
13. Cayce KA, Feldman SR, McMichael AJ. Hyperpigmentation: a review
was more effective in the middle to deep dermal of common treatment options. J Drugs Dermatol 2004;3:668–73.
pigmentations of skin. This was supported by the 14. Briganti S, Camera E, Picado M. Chemical and instrumental approaches
general fact that the Q-switched Nd:YAG at 1,064- to treat hyperpigmentation. Pigment Cell Res 2003;16:101–10.
nm was best for treating darkly pigmented skin 15. Ostovari N, Mohtasham N, Shahidi Oadras M, Malekzad F. 532-nm
and 1064-nm Q-switched Nd:YAG laser therapy for reduction of
because of the lower risk of subsequent induction of pigmentation in macular amyloidosis patches. J Eur Acad Dermatol
pigmentary changes.24 In conclusion, the 1,064-nm Venereol 2008;22:442–6.
Q-switched Nd:YAG laser is a suitable and effective 16. Sharquie KE, Al-Tikreety MM, Al-Mashhadani SA. Lactic acid as a new
therapeutic peeling agent in melasma. Dermatol Surg 2005;31:149–54.
mode of therapy for treating dermal melanosis in
patients with Lifa disease. 17. Khoo BP, Tay YK, Goh CL. Calcipotriol ointment vs. betamethasone
7-valerateointment in the treatment of lichen amyloidosis. Int J
Dermatol 1999;38:539–41.
18. Jin AG, Por A, Wee LK, Kai CK, et al. Comparative study of
phototherapy (UVB) vs. photochemotherapy (PUVA) vs. topical steroids
References in the treatment of primary cutaneous lichen amyloidosis.
Photodermatol Photoimmunol Photomed 2001;17:42–3.
1. Kurita M, Kato H, Yoshimura K. A therapeutic strategy based on
histological assessment of hyper-pigmented skin lesions in Asians. J Plast 19. Aram H. Failure of etretinate (RO 10–9359) in lichen amyloidosis. Int J
Reconstr Aesthet Surg 2009;62:955–63. Dermatol 1998;25:206.
2. Fitzpatrick TB, Ortonne JP. Normal skin color and general 20. Wong CK, Li WM. Dermabrasion for lichen amyloidosis. Arch
considerations of pigmentary disorders. In: Freedberg IM, Eisen AZ, Dermatol 1982;118:302–4.
Wolf K, Austin KF, et al, editors. Fitzpatrick’s dermatology in
general medicine (6th Ed). New York: McGraw-Hill; 2003; pp. 21. Arora P, Sarkar R, Garg VK, Arya L. Lasers for treatment of melasma
819–25. and postinflammatory hyperpigmentation. J Cutan Aesthet Surg 2012;
5:93–103.
3. Al-Aboosi M, Abalkhail A, Kasiffi O, Al-Khatib A, et al. Frictional
melanosis: a clinical, histologic, and ultrastructural study in Jordanian 22. Anderson RR. Laser in dermatology: a critical update. J Dermatol 2000;
patients. Int J Dermatol 2004;43:261–4. 27:700–5.
4. Sharquie KE. Frictional dermal melanosis (lifa disease) over bony 23. Cencic B, Lukac M, Marincek M, Vizintin Z. High fluence, high beam
prominences. J Fac Med Baghdad 1993;35:83–7. quality Q switched Nd:YAG laser with optoflex delivery system for
treating benign pigmented lesions and tattoos. J LAHA 2010;2010:9–18.
5. Sharquie KE, Al-Dorky MK. Frictional dermal melanosis (lifa disease)
over bony prominences. J Dermatol 2001;28:12–5. 24. Alexiades-Armenakas MR, Dover JS, Arndt KA. Laser therapy. In:
Bolognia JL, Jorizzo JL, Rapini RP, (eds). Dermatology (2th ed). Saint
6. Siragusa M, Ferri R, Cavallari V, Schepis C. Friction melanosis, Louis, MO: Mosby Elsevier, 2008;2:2099–120.
frictional amyloidosis, macular amyloidosis, towel melanosis: many
names for the same clinical entity. Eur J Dermatol 2001;11:545–8.
7. Magana-Garcia M, Carrasco G, Herreva-Goepfert R, Pueblitz-Peredo S. Address correspondence and reprint requests to: Muhsin A.
Hyperpigmentation of the clavicular zone: a variant of friction
Al-Dhalimi, MD, Department of Dermatology, Faculty of
melanosis. Int J Dermatol 1989;28:119–22.
Medicine, University of Kufa, PO Box 21, Kufa Post Office,
8. Hidano A, Mizuguchi M, Higaki Y, Friction melanosis [in French]. Ann 12224, Najaf, Iraq, or e-mail: muhsin.aldhalimi@uokufa.
Dermatol Venereol 1984;111:1063–71. edu.iq
Copyright © American Society for Dermatologic Surgery. Unauthorized reproduction of this article is prohibited.
View publication stats