eISSN: 2299-0046
ISSN: 1642-395X
Advances in Dermatology and Allergology/Postępy Dermatologii i Alergologii
Current issue Archive Manuscripts accepted About the journal Editorial board Journal's reviewers Abstracting and indexing Subscription Contact Instructions for authors
SCImago Journal & Country Rank
vol. 36
Original paper

How frequently does palmoplantar psoriasis affect the palms and/or soles? A systematic review and meta-analysis

Zorica Sojević Timotijević
Goran Trajković
Janko Jankovic
Milijana Relić
Dragica Đorić
Danica Vukićević
Goran Relić
Dragiša Rašić
Milan Filipović
Slavenka Janković

Department of Dermatology, Faculty of Medicine, University of Priština, Kosovska Mitrovica, Serbia
Institute of Medical Statistics and Informatics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Institute of Social Medicine, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Institute of Pathology, Faculty of Medicine, University of Priština, Kosovska Mitrovica, Serbia
Department of Gynecology, Faculty of Medicine, University of Priština, Kosovska Mitrovica, Serbia
Department of Internal Medicine, Faculty of Medicine, University of Priština, Kosovska Mitrovica, Serbia
Department of Surgery, Faculty of Medicine, University of Priština, Kosovska Mitrovica, Serbia
Institute of Epidemiology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia
Adv Dermatol Allergol 2019; XXXVI (5): 595-603
Online publish date: 2019/11/12
Article file
- How frequently.pdf  [0.20 MB]
Get citation
JabRef, Mendeley
Papers, Reference Manager, RefWorks, Zotero


Palmoplantar psoriasis (PPP) is a variant of psoriasis located on the palms and/or soles which often occurs along with psoriasis elsewhere on the body and less commonly may be the only skin manifestation [1, 2]. The prevalence of PPP in psoriasis patients varies between studies from 2.8% to 40.9% [3]. The lesions of PPP are typically bilaterally symmetrical, although unilateral involvement may be seen [3]. PPP can express many different morphologic patterns ranging from thick hyperkeratotic plaques to pustular lesions with a spectrum of overlapping of both [1, 4, 5]. Unlike chronic plaque psoriasis, PPP has a significant discordance between body surface area (BSA) involvement and impact on health-related quality of life (QoL) [1]. Even though PPP involves a small percentage of the BSA, patients with this condition are more likely to suffer from greater QoL impairment than those with moderate-to-severe plaque psoriasis [6], and have significantly higher impairment at work/hobbies [7]. According to Pettey et al. [8], the unique impact of PPP involvement beyond common plaque psoriasis is primarily physical with a greater physical dysfunction and physical discomfort. Only a few studies compared QoL between patients with PPP on the palms and the soles. In the study of American psoriasis patients, QoL was overall more impaired due to psoriasis on the palms than on the soles [9], while the opposite was true in the study of Serbian psoriasis patients [10].
Although PPP is a disabling variant of psoriasis and therapeutically challenging condition which is often recalcitrant to various topical and systematic therapy [11–13], its epidemiology is poorly defined.


The aim of this systematic review and meta-analysis was to estimate the prevalence of PPP for each single location (palms or soles or both) and to find out which one is the most prevalent. In addition, we were interested to know the gender more affected by the PPP and the most common morphological type of this condition.

Material and methods

The present systematic review and meta-analysis were conducted in accordance with Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [14].

Identification of studies

The MEDLINE (via PubMed), and Elsevier’s abstract and citation database SCOPUS were searched from inception to October 2017 by two independent investigators (Sojeviæ Timotijeviæ Z, Trajkoviæ G). The following search terms were used: psoriasis[ti] palmoplantar*[ti]. Searching was restricted to English and French language articles. There was no restriction on the type of psoriasis and patients age. We manually searched the references of all selected articles to identify other relevant studies.

Inclusion and exclusion criteria

Inclusion criteria of the selected studies were: (1) at least one sample of psoriatic patients designated as palmoplantar psoriasis; (2) published data on absolute frequency or proportion of number of patients with psoriasis involvement of (a) palms, (b) soles, and (c) both, or possibility to reconstruct such numbers based on the available data. The criterion for exclusion was the inability to find numbers or proportions of patients with PPP by single locations (palms, soles, or both).

Data extraction and analysis

While the titles and abstracts met the inclusion criteria, full-text articles were searched and screened independently by two investigators (Sojeviæ Timotijeviæ Z, Trajkoviæ G) to confirm eligibility and any disagreement was resolved by consensus or a third opinion (Jankoviæ S).
The following information was extracted: first author, year of publication, origin of the study, study design, study date, study population (sample size, percentage of men and women, mean age and/or age range of subjects), clinical type of psoriasis, PPP involvement of palms, soles, and both, involvement of the rest of the body, and baseline disease measures.
We used qualitative analysis to aggregate findings from selected studies and the random effects weighted analysis to obtain the pooled proportions with 95% confidence intervals (CI) of affected sites (palms, soles, and both), illustrated in a forest plot. The method of Barendregt and Doi [15] for meta-analysis of multiple categories was applied.


In total 293 relevant articles that fit our search strategy were identified. The procedure for identifying and selecting eligible studies is shown in Figure 1. After removal of duplicates (126 records), 167 articles remained for screening. A further 11 articles were excluded through abstract screening. Of 156 articles available for full-text reading, 132 articles were excluded according to exclusion criteria. Finally, a total of 24 articles that fulfilled criteria were included in our systematic review [1, 3, 12, 16–36]. Out of 24 studies, 21 were included in the meta-analysis, while three studies did not fulfil the inclusion criteria [1, 16, 25] since data on involvement of palms and/or soles could not be precisely extracted for all PPP cases.
The basic characteristics of all 24 studies included in the review are presented in Table 1. Seven studies were intervention studies; the remaining 17 were observational in design. The included studies were conducted in 13 different countries (8 studies were from India, 2 from the USA, 2 from Israel, 2 from Austria, 2 from Germany and one study from each of the following countries: Japan, Canada, Kuwait, France, England, Italy, and Turkey). One study was a joint study from Italy and Austria.
All listed studies comprised a total of 2083 patients with PPP. According to available data from 22 studies, more males (1072) than females (841) were affected by PPP. For 170 patients from two studies, gender data were not available. The statistically significant predominance of men was noted in nine studies, while the predominance of women was seen in two studies. Ages of patients ranged from 8 [26] up to 87 years [30], whereas the mean age ranged from 37.4 years [17] to 58.5 years [20]. With the exception of two studies [25, 31], all the remaining studies reported a clinical type/s of PPP as plaque/hyperkeratotic, pustular or mixed. The most common was the plaque/hyperkeratotic type.
In most studies (20) all three locations: palms, soles and both were affected by psoriasis, whereas in 4 remaining studies only two locations in each study were affected: palms and both palms and soles [18, 24], and soles and both palms and soles [28, 34]. Most studies (17) confirmed the involvement of the rest of the body, while data were not available in 7 studies.
To assess severity of PPP, different measures were used, such as involved palmoplantar surface area (PPSA), involved BSA outside the palmoplantar region, physician’s global assessment (PGA) score for extra-palmoplantar lesions, psoriasis area and severity index (PASI), modified palmoplantar (pustular) psoriasis area and severity index (m-PPPASI), severity index (SI), erythema, scaling and induration (ESI) score; and erythema, scaling, induration and fissuring (ESIF) score. In addition, two QoL instruments were used: dermatology life quality index (DLQI), and palmar-plantar QoL index (PPQoLI). For the body involvement with psoriasis, different cutoff levels were reported: four cutoff levels for the involvement of PPSA: ≥ 10% [19], ≥ 30% [26, 27], > 30% [23, 32], and ≥ 50% [1, 12]; and two cutoff levels for the involvement of BSA outside the palms and soles: ≤ 5% [21, 23, 26, 32], and ≤ 30% [3, 31]. PGA score for extra-palmoplantar lesions was used in three studies [19–21], and m-PPPASI was used in two studies [12, 19]. Most studies used more than one measure. Only six studies [3, 23–25, 35, 36] reported data on unilateral/bilateral distribution of lesions on palms and soles, with more frequent bilateral lesions.

Prevalence of PPP in all psoriasis patients

The prevalence of PPP as a part of a larger study on psoriasis was noted in six studies included in this analysis [1, 3, 12, 16, 17, 35]. It ranged from 10.1% [17] to 59% [35], and even to 76% [12] of all psoriasis patients.

Prevalence of PPP locations

Most studies (18) reported that the prevalence of PPP of both palms and soles was higher (ranging from 15% to 96%), than the prevalence of palmar or plantar single location (ranging from 0 to 50% and from 0 to 44%, respectively) (Table 1).
When considering the 21 studies included in the meta-analysis, the highest PPP prevalence was seen for both palms and soles involvement (59%; 95% CI: 47–67). The prevalence of each single location, i.e. of palms (21%; 95% CI: 13–30), and of soles (20%; 95% CI: 12–29) involvement was almost equal. Random effects pooling was used due to significant heterogeneity (Q = 298.38; p < 0.001, I2 = 93%). The proportions of PPP in individual studies and their weighted average by specific locations are shown in Figure 2.


The prevalence of PPP locations showed high variability between studies varying from 15% to 96% when considering both palms and soles, while the palms and soles involvement was seen from 0% to 50%, and from 0% to 44%, respectively.
The meta-analysis revealed that the prevalence of PPP of both palms and soles (59%) was almost three times higher than the prevalence of any single location of PPP, i.e. either palms (21%) or soles (20%) involvement. However, there was no statistically significant difference between palmar and plantar involvement (80% vs. 79%), which is in accordance with several studies from the West [37, 38]. In contrast, Indian authors reported that plantar involvement in their patients was twice more common than palmar involvement, and attributed this to the Indian custom of walking barefoot or wearing open slippers most of the time [3, 39].
There is a paucity of information about gender differences in psoriasis [40], especially in localized psoriasis variants such as PPP [41]. Our results suggest that more males than females were affected by PPP. This topic should deserve more attention in the future, with special focus on the practical implications that gender-specific characteristics may have on the prognosis and therapy of PPP [40].
According to the results of this review, ages of patients ranged from 8 to 87 years, which is in accordance with the previous finding that PPP affects individuals of all ages [41]. In the study by Chung et al. [6], patients with PPP were older than patients with plaque psoriasis with mean ages of 53.8 years vs. 48.7 years, respectively.
PPP can be seen in many different clinical forms [5]. It features hyperkeratotic, pustular, or mixed morphologies [41]. In this review, patients displayed predominantly plaque/hyperkeratotic palmoplantar lesions, followed by pustular lesions and their combination (plaque/pustular). Only in two studies [20, 34], pure palmoplantar pustulosis is recognised as a subtype of psoriasis, which is in agreement with other studies [42, 43]. The results of a study conducted by Brunasso et al. [21] suggest a close relationship between PPP and palmoplantar pustulosis and that the existing data concerning epidemiology, clinical presentation, genetics, histopathology and pathogenesis do not permit a clear distinction between these two entities. However, most genetic studies in last two decades have provided evidence that palmoplantar pustulosis is a disease distinct from psoriasis [44–49]. According to a recently published systematic review of palmoplantar pustulosis, there are no sufficient data to exclude this condition from the psoriasis group [50]. Future studies are needed to elucidate this still controversial issue.
PPP may exist separately or may be associated with psoriasis elsewhere on the body [5]. Almost 40% of the patients from 15 studies included in this review had an isolated form of PPP without lesions elsewhere. Kumar et al. [3] reported the highest percentage of the patients (almost 70%) with isolated PPP as a consequence of longer persistence/refractory nature of lesions at palms and/or soles.
There is no universally accepted definition of mild, moderate and severe PPP. It is well known that PPP severity appeared independent from the degree of BSA involvement [1] and that even mild psoriasis located on the palms and/or soles frequently needs more intensive therapy than does psoriasis elsewhere [4]. For the assessment of PPP severity, different traditional measures with different cutoff levels were used in the studies included in this review. However, the researchers agreed that the level of functional impairment should be taken into account, rather than relying on traditional measures [1, 4, 6]. Two assessment tools specifically tailored to patients with PPP were developed to help clinicians to measure the severity of PPP and response to treatment: m-PPPASI [19, 51] and PPQoLI [1].
The lesions of PPP are almost always bilaterally symmetrical, which was well illustrated in all studies with available data, with a high percentage of patients showing this pattern (100% in the studies by Wilkinson et al. [36], Hofer et al. [24], and Haseena et al. [23]; and between 79% and 96% in the studies by Khandpur and Sharma [25], Venkatesan et al. [35], and Kumar et al. [3].
This is the first systematic review and meta-analysis of the PPP prevalence according to the affected locations and basic epidemiological and morphological characteristics. However, the results of this review should be considered in light of some limitations. Our sample was not comprehensive. We focused in our literature search on the terms “palmoplantar” and “psoriasis”, and only papers written in English and French language were considered.


According to our results, even three fifths of all PPP patients had involvement of both palms and soles (59%), while two fifths of them had either the palm (21%) or sole (20%) involvement. Males were more affected by PPP than females. The data concerning the percentage of involved PPSA and BSA outside the PPSA, as well as data concerning unilateral/bilateral involvement of the palms and/or soles, were lacking in most studies. Also there is no consistency between studies in determining disease measures used as inclusion criteria, and their cutoff values. Future research should be performed to elucidate basic epidemiological characteristics of PPP and to assess which location of PPP (palms or soles) causes greater physical discomfort and functional disability which probably would be helpful for proper consideration of this debilitating and therapeutically challenging condition.


This work was supported by the Ministry of Education, Science and Technological Development of the Republic of Serbia (project No. 175025).

Conflict of interest

The authors declare no conflict of interest.


1. Farley E, Masrour S, McKey J, Menter A. Palmoplantar psoriasis: a phenotypical and clinical review with introduction of a new quality-of-life assessment tool. J Am Acad Dermatol 2009; 60: 1024-31.
2. Griffiths CE, Christophers E, Barker JN, et al. A classification of psoriasis vulgaris according to phenotype. Br J Dermatol 2007; 156: 258-62.
3. Kumar B, Saraswat A, Kaur I. Palmoplantar lesions in psoriasis: a study of 3065 patients. Acta Derm Venereol 2002; 82: 192-5.
4. Menter A, Griffiths CE. Current and future management of psoriasis. Lancet 2007; 370: 272-84.
5. Engin B, Aşkın Ö, Tüzün Y. Palmoplantar psoriasis. Clin Dermatol 2017; 35: 19-27.
6. Chung J, Callis Duffin K, Takeshita J, et al. Palmoplantar psoriasis is associated with greater impairment of health-related quality of life compared with moderate to severe plaque psoriasis. J Am Acad Dermatol 2014; 71: 623-32.
7. Sampogna F, Tabolli S, Abeni D. Living with psoriasis: prevalence of shame, anger, worry, and problems in daily activities and social life. Acta Derm Venereol 2012; 92: 299-303.
8. Pettey AA, Balkrishnan R, Rapp SR, et al. Patients with palmoplantar psoriasis have more physical disability and discomfort than patients with other forms of psoriasis: implications for clinical practice. J Am Acad Dermatol 2003; 49: 271-5.
9. Gottlieb A, Sullivan J, van Doorn M, et al. Secukinumab shows significant efficacy in palmoplantar psoriasis: results from GESTURE, a randomized controlled trial. J Am Acad Dermatol 2017; 76: 70-80.
10. Sojeviæ Timotijeviæ Z, Jankoviæ S, Trajkoviæ G, et al. Identification of psoriatic patients at risk of high quality of life impairment. J Dermatol 2013; 40: 797-804.
11. Rapp SR, Feldaman SR, Exum ML, et al. Psoriasis causes as much disability as other major medical disease. J Am Acad Dermatol 1999; 41: 401-7.
12. Janagond AB, Kanwar AJ, Handa S. Efficacy and safety of systemic methotrexate vs. acitretin in psoriasis patients with significant palmoplantar involvement: a prospective, randomized study. J Eur Acad Dermatol Venereol 2013; 27: e384-9.
13. Sezer E, Erbil AH, Kurumlu Z, et al. Comparison of the efficacy of local narrowband ultraviolet B (NB-UVB) phototherapy versus psoralen plus ultraviolet A (PUVA) paint for palmoplantar psoriasis. J Dermatol 2007; 34: 435-40.
14. Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 2009; 6: e1000097.
15. Barendregt JJ, Doi SA. Meta XL User Guide, version 5.3 [Computer software]. 2016. Available at https://epigear.com/index_files/metaxl.html (accessed 29 May 2018).
16. Adisen E, Tekin O, Gulekon A, Gürer MA. A retrospective analysis of treatment responses of palmoplantar psoriasis in 114 patients. J Eur Acad Dermatol Venereol 2009; 23: 814-9.
17. Al-Mutairi N, Abdalla TO, Nour TM. Resistant palmoplantar lesions in patients of psoriasis: evaluation of the causes and comparison of the frequency of delayed-type hypersensitivity in patients without palm and sole lesions. Med Princ Pract 2014; 23: 561-7.
18. Angelovska I, Mahler V. Occupational palmoplantar psoriasis: a clinical case series with consideration of the S1 guidelines on expert medical assessments of occupational psoriasis. J Dtsch Dermatol Ges 2014; 12: 697-708.
19. Bissonnette R, Poulin Y, Guenther L, et al. Treatment of palmoplantar psoriasis with infliximab: a randomized, double-blind placebo-controlled study. J Eur Acad Dermatol Venereol 2011; 25: 1402-8.
20. Brunasso AM, Massone C. Can we really separate palmoplantar pustulosis from psoriasis? J Eur Acad Dermatol Venereol 2010; 24: 619-21.
21. Brunasso AM, Puntoni M, Aberer W, et al. Clinical and epidemiological comparison of patients affected by palmoplantar plaque psoriasis and palmoplantar pustulosis: a case series study. Br J Dermatol 2013; 168: 1243-51.
22. Coleman WR, Lowe NJ, David M, Halder RM. Palmoplantar psoriasis: experience with 8-methoxypsoralen soaks plus ultraviolet A with the use of a high-output metal halide device. J Am Acad Dermatol 1989; 20: 1078-82.
23. Haseena K, George S, Riyaz N, et al. Methotrexate iontophoresis versus coal tar ointment in palmoplantar psoriasis: a pilot study. Indian J Dermatol Venereol Leprol 2017; 83: 569-73.
24. Hofer A, Fink-Puches R, Kerl H, et al. Paired comparison of bathwater versus oral delivery of 8-methoxypsoralen in psoralen plus ultraviolet: a therapy for chronic palmoplantar psoriasis. Photodermatol Photoimmunol Photomed 2006; 22: 1-5.
25. Khandpur S, Sharma VK. Comparison of clobetasol propionate cream plus coal tar vs. topical psoralen and solar ultraviolet A therapy in palmoplantar psoriasis. Clin Exp Dermatol 2011; 36: 613-6.
26. Kumar B, Kumar R, Kaur I. Coal tar therapy in palmoplantar psoriasis: old wine in an old bottle? Int J Dermatol 1997; 36: 309-12.
27. Kumar B, Sandhu K, Kaur I. Topical 0.25% methotrexate gel in a hydrogel base for palmoplantar psoriasis. J Dermatol 2004; 31: 798-80.
28. Lawrence CM, Marks J, Parker S, Shuster S. A comparison of PUVA-etretinate and PUVA-placebo for palmoplantar pustular psoriasis. Br J Dermatol 1984; 110: 221-6.
29. Lior S, Grigory K, Pnina S, et al. Therapeutic hotline. Alefacept in the treatment of hyperkeratotic palmoplantar psoriasis. Dermatol Ther 2010; 23: 556-60.
30. Lozinski A, Barzilai A, Pavlotsky F. Broad-band UVB versus paint PUVA for palmoplantar psoriasis treatment. J Dermatolog Treat 2016; 27: 221-3.
31. Nisticò SP, Saraceno R, Stefanescu S, Chimenti S. A 308-nm monochromatic excimer light in the treatment of palmoplantar psoriasis. J Eur Acad Dermatol Venereol 2006; 20: 523-6.
32. Ravi Kumar BC, Kaur I, Kumar B. Topical methotrexate therapy in palmoplantar psoriasis. Indian J Dermatol Venereol Leprol 1999; 65: 270-2.
33. Redon E, Bursztejn AC, Loos C, et al. A retrospective efficacy and safety study of UVB-TL01 phototherapy and PUVA therapy in palmoplantar psoriasis. Ann Dermatol Venereol 2010; 137: 597-603.
34. Tanaka N, Fujioka A, Tajima S, et al. Levels of proelafin peptides in the sera of the patients with generalized pustular psoriasis and pustulosis palmoplantaris. Acta Derm Venereol 2000; 80: 102-5.
35. Venkatesan A, Aravamudhan R, Perumal SK, et al. Palmoplantar psoriasis- ahead in the race – a prospective study from a tertiary health care centre in South India. J Clin Diagn Res 2015; 9: WC01-3.
36. Wilkinson JD, Ralfs IG, Harper JI, Black MM. Topical methoxsalen photochemotherapy in the treatment of palmoplantar pustulosis and psoriasis. Acta Derm Venereol 1979; Suppl 59: 193-8.
37. Molin L. Psoriasis. A study of the course and degree of severity, joint movements, socio-medical conditions, general morbidity and infuences of selection factors among previously hospitalized psoriatics. Acta Derm Venereol 1972; 53 Suppl 72: 1-25.
38. Farber EM, Nall ML. The natural history of psoriasis in 5,600 patients. Dermatologica 1974; 148: 1-18.
39. Kaur I, Handa S, Kumar B. Natural history of psoriasis: a study from the Indian subcontinent. J Dermatol 1997; 24: 230-4.
40. Colombo D, Cassano N, Bellia G, Vena GA. Gender medicine and psoriasis. World J Dermatol 2014; 3: 36-44.
41. Miceli A, Schmieder J. Palmoplantar psoriasis. StatPearls [Internet] Publishing LLC. 2017. Available at: https://www.ncbi.nlm.nih.gov/books/NBK448142/
42. Christophers E, Mrowietz U. Psoriasis. In: Braun Falco’s Dermatology. Burgdorf WHC, Plewig G, Wolff HH, Landthaler M (eds). Springer, New York 2009; 506-26.
43. Bissonnette R, Suárez-Fariñas M, Li X, et al. Based on molecular profiling of gene expression, palmoplantar pustulosis and palmoplantar pustular psoriasis are highly related diseases that appear to be distinct from psoriasis vulgaris. PLoS One 2016; 11: e0155215.
44. Asumalahti K, Ameen M, Suomela S, et al. Genetic analysis of PSORS1 distinguishes guttate psoriasis and palmoplantar pustulosis. J Invest Dermatol 2003; 120: 627-32.
45. Mossner R, Kingo K, Kleensang A, et al. Association of TNF-238 aand -308 promoter polymorphisms with psoriasis vulgaris and psoriatic arthritis but not with pustulosis palmoplantaris. J Invest Dermatol 2005; 124: 282-4.
46. de Waal AC, van de Kerkhof PC. Pustulosis palmoplantaris is a disease distinct from psoriasis. J Dermatolog Treat 2011; 22: 102-5.
47. Marsland AM, Chalmers RJ, Hollis S, et al. Interventions for chronic palmoplantar pustulosis. Cochrane Database Syst Rev 2006; 1: CD001433.
48. Ammoury A, El Sayed F, Dhaybi R, Bazex J. Palmoplantar pustulosis should not be considered as a variant of psoriasis. J Eur Acad Dermatol Venereol 2008; 22: 392-3.
49. Yamamoto T. Extra-palmoplantar lesions associated with palmoplantar pustulosis. J Eur Acad Dermatol Venereol 2009; 23: 1227-32.
50. Misiak-Galazka M, Wolska H, Rudnicka L. What do we know about palmoplantar pustulosis? J Eur Acad Dermatol Venereol 2017; 31: 38-44.
51. Brunasso AM, Salvini C, Massone C. Efalizumab for severe palmoplantar psoriasis: an open-label pilot trial in five patients. J Eur Acad Dermatol Venereol 2009; 23: 415-9.
Copyright: © 2019 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2020 Termedia Sp. z o.o. All rights reserved.
Developed by Bentus.
PayU - płatności internetowe