Compartilhar
Informação da revista
Vol. 97. Núm. 3.
Páginas 307-314 (01 Maio 2022)
Compartilhar
Compartilhar
Baixar PDF
Mais opções do artigo
Visitas
...
Vol. 97. Núm. 3.
Páginas 307-314 (01 Maio 2022)
Original Article
Open Access
Sensitizing agents found in children and adolescents with recalcitrant atopic dermatitis: a cross-sectional study with a pediatric battery
Visitas
...
Cristiane Almeida Soares Cattania,b,
Autor para correspondência
crisalmeidacattani@gmail.com

Corresponding author.
, Kenselyn Oppermanna, Simone Perazzolia, Nathalia Hoffmann Guardaa, Paula Baréaa, Renan Rangel Bonamigob,c
a Sanitary Dermatology Outpatient Clinic, Secretaria da Saúde do Estado do Rio Grande do Sul, Porto Alegre, RS, Brazil
b Postgraduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil
c Faculty of Medicine, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil
Informação do artigo
Resume
Texto Completo
Bibliografia
Baixar PDF
Estatísticas
Tabelas (3)
Table 1. Brazilian pediatric battery – based on EAACI consensus.12,18
Table 2. Atopic dermatitis and patch tests: sample characteristics (n = 54) and associations.
Table 3. Allergen profile: positive tests in relation to sex and age groups.
Mostrar maisMostrar menos
Abstract
Background

Atopic dermatitis is the most common inflammatory skin disease in childhood and has an important impact on quality of life, especially severe cases or those that are recalcitrant to treatments. Sensitization to allergens with the potential for allergic contact dermatitis is a factor associated with cases of recalcitrant atopic dermatitis. Understanding the relationship between atopic dermatitis, allergens, and allergic contact dermatitis is essential. In Brazil, there are no studies on sensitization to allergens found in patch tests with pediatric batteries in patients with atopic dermatitis.

Objectives

To verify the main sensitizing agents, the prevalence of allergic contact dermatitis and the epidemiological and clinical profile of children and adolescents with atopic dermatitis.

Methods

Cross-sectional, prospective study in patients between 4 and 18 years of age, with recalcitrant atopic dermatitis, treated at the Sanitary Dermatology Outpatient Clinic (RS). All patients underwent patch tests with a battery of pediatric allergens.

Results

The prevalence of sensitization and allergic contact dermatitis in the evaluated patients was 37.07% (20/54) and 27.7% (15/54), respectively. The most frequent allergens were: nickel sulfate (16.7%), disperse blue (5.6%), and fragrance mix I (5.6%). Nickel was associated with the female sex (p = 0.019).

Study limitations

Sample size and selection, absence of a control group.

Conclusions

A proportion of patients with recalcitrant atopic dermatitis may be sensitized to different allergens and may even have developed allergic contact dermatitis. Recognizing this context is important in the prevention strategy and management of the disease.

Keywords:
Adolescent
Child
Dermatitis, allergic contact
Dermatitis, atopic
Patch tests
Texto Completo
Introduction

Atopic dermatitis (AD) and allergic contact dermatitis (ACD) are two of the most common inflammatory skin diseases in the pediatric population with a complex interrelationship.1,2

The prevalence of AD has increased significantly over the past thirty years, affecting between 15% and 30% of children in Western countries.3 Likewise, ACD is frequent in both the adult and pediatric populations, including reports even in children of younger ages.4,5 Recent studies have reported an increase in the prevalence of ACD in symptomatic children ranging from 27% to 95%, 6%.5–8

Given the skin barrier dysfunction that decreases the protection against environmental agents, irritative contact dermatitis (ICD) and allergic contact dermatitis (ACD) are significant problems among individuals with AD.5,9

Clinically, AD and ACD may be indistinguishable, and concomitant allergic reactions have been described as possible causes of recalcitrant or therapy-resistant atopic dermatitis.1,10,11

Although there are no evidence-based consensus guidelines for patch tests (PT) in children, it is a safe and useful tool for identifying skin sensitization.5,12

Most studies on the prevalence and clinical and epidemiological characteristics of ACD in children and adolescents with AD are retrospective and come from North American and European centers.1,2,5

In Brazil, there are few studies on ACD in the pediatric population, and all of them performed PT using the standard Brazilian batteries used in adults or batteries of cosmetics; to date, there are no records of studies that have used PT pediatric batteries in Brazil.7,13–15 It is worth emphasizing the importance of knowing the sensitizers in each country, given the variability of exposures and differences between regions of the world.

The present study aims to verify the sensitizers and the presence of ACD in children and adolescents with recalcitrant AD, in addition to their epidemiological and clinical profile, in a southern Brazilian sample that was submitted to a pediatric patch test battery series.

Materials and methods

This is a prospective, cross-sectional study carried out with patch tests in patients with recalcitrant atopic dermatitis, aged between 4 and 18 years, treated at the Sanitary Dermatology Outpatient Clinic, Porto Alegre, State of Rio Grande do Sul (Brazil), between February 2019 and March 2020.

This study was approved by the Research Ethics Committees of the Health Secretariat of the State of Rio Grande do Sul and Universidade Federal de Ciências da Saúde de Porto Alegre (Counsels number 3,091,016 and 3,084,699, respectively). Only patients whose parents/legal guardians signed the consent form were evaluated. Anamnesis and physical examination were performed at the first consultation.

The selected patients were those diagnosed with atopic dermatitis, following the modified criteria of Hanifin and Rajka,16 and those who had a history of recalcitrant dermatitis (or dermatitis that recurred soon after discontinuation of topical treatment) and, therefore, had a clinical suspicion of allergic contact dermatitis.10–12 Patients using corticosteroids or topical immunomodulators within the last seven days, systemic immunosuppressants or corticosteroids within the last 30 days, those exposed to ultraviolet radiation 15 days before the test, those who had dermatitis at the test site, history of anaphylaxis, psychiatric disorders or pregnancy were excluded.12

The variables collected were: age, sex, age at onset and duration of dermatitis, presence of other associated atopic diseases, and family history of atopic diseases. Moreover, the following were evaluated: skin phototype, the topography of dermatitis, and AD severity through the Eczema Area and Severity Index (EASI) by body region (face and cervical region, upper limbs, lower limbs, and trunk), which can vary from 0% to 100%; Intensity of each lesion (erythema, edema or papules, excoriation and lichenification), on a scale of 0 to 3. The sum of the points classifies the disease as very mild (0.1 to 1); mild (1.1 to 7); moderate (7.1 to 20); severe (21.1 to 50); or very severe 50.1 to 72).17

PTs were performed using a modified pediatric battery, based on the consensus of the European Academy of Allergology and Clinical Immunology (EAACI) Task Force on Allergic Contact Dermatitis in Children on recommendations for patch testing with a battery of major allergens in the pediatric group.12 The battery was developed by the company IPI -ASAC BrasilR and adapted according to the availability of the products in Brazil. It consists of 20 substances, including allergens and mixtures (Table 1).18 Some substances are present in the Brazilian standard battery,19 but others do not exist regionally, such as bufexamac (an anti-inflammatory agent) and Tixocortol pivalate (group A corticosteroid), which were removed. This was replaced by hydrocortisone (same group A). One component of the Compositae mixture was also excluded due to lack of the raw material. The allergens were inserted into 8-mm chambers in Alergo Chamber containers (NeoflexR).

Table 1.

Brazilian pediatric battery – based on EAACI consensus.12,18

Substance  Concentration. (%)  Vehicle 
1- Hydrocortisone acetate  25.0  Vaseline 
2- Lanolin  30.0  Vaseline 
3- Disperse blue  1.0  Vaseline 
4- Potassium bichromate  0.5  Vaseline 
5- Budesonide  0.1  Vaseline 
6- P-tert-butylphenol formaldehyde resin  1.0  Vaseline 
7- Colophony  20.0  Vaseline 
8- Compositae mix  1.9  Vaseline 
9- Fragrance mix II  14.0  Vaseline 
10- Mercaptobenzothiazole  2.0  Vaseline 
11- Lyral  5.0  Vaseline 
12- Mercapto mix  2.0  Vaseline 
13- Methylchloroisothiazolinone/Methylisothiazolinone  1.0  Water 
14- Methyldibromo glutaronitrile  1.0  Vaseline 
15- Neomycin  20.0  Vaseline 
16- P-phenylenediamine  0.5  Vaseline 
17- Fragrance mix I  7.0  Vaseline 
18- Sesquiterpene Lactone Mix  0.1  Vaseline 
19- Nickel sulfate  5.0  Vaseline 
20- Tiuram mix  1.0  Vaseline 

The procedures were performed according to the recommendations of the International Contact Dermatitis Group (ICDRG).12 The containers were applied to the dorsal area of the patients and removed within 48 hours. The readings were performed at 48 hours and at 96 hours, both by the same dermatologists. Tests with reactions classified as +, ++ or +++ were considered positive. Only the results of the 96 -h readings were included in the statistical analysis. Patients with ACD were considered to be those who tested positive within 96 hours with currently relevant allergens (exposure to allergens that explained the clinical picture at the time). Those with no current relevance were classified as sensitized but not having ACD.

Data analysis was performed using the SPSS software, version 25. The chi-square test or Fisher’s test were used for categorical variables. For continuous variables, the Mann-Whitney test was used. Values ​​of p < 0.05 were considered statistically significant.

Results

Fifty-four patients with AD were evaluated. Using the World Health Organization classification,7 the sample was divided into two age groups: children (4 to 9 years old) and adolescents (10 to 18 years old), of which 31 (57.4%) were children and 23 (42.6%) were adolescents (Table 2). The female sex predominated with 35 patients (64.8%), as well as phototypes III and IV, with 15 (27.8%) and 21 (38.9%) patients, respectively. The mean age of AD onset was 2.63 years (SD = 2.7), with a median of 1.5 years. The mean duration of AD was 6.57 years (SD = 4.2) with a median of 5 years.

Table 2.

Atopic dermatitis and patch tests: sample characteristics (n = 54) and associations.

Variables  Category(n)  Negative tests (n)  Positive tests n (%)  Statistical test  p-value 
SexMale (19)  17  2 (10.5)     
Female (35)  22  13 (37.1)  χ2=3.123  0.077 
Age group4–9 y (31)  20  11 (35.5)     
10–18 y (23)  19  4 (17.5)  χ2=1.347  0.246 
PhototypeI (2)  1 (50)     
II (4)     
III (15)  11  4 (26.6)     
IV (21)  14  7 (33.3)  χ2=5.46  0.361 
V (11)  2 (18.2)     
VI (1)  1 (100)     
Personal atopyaYes (45)  32  13 (28.8)  Fisher  1.0 
No (9)  2 (22.2)     
Familial atopyYes (35)  23  12 (34.2)  χ2=1.279  0.258 
No (19)  16  3 (15.8)     
EASI scoreMild (19)  14  5 (26.3)     
Moderate (25)  18  7 (28)  χ2= 0.544  0.901 
Severe (9)  3 (33)     
Very severe (1)     
Site of dermatitisFace/Cervical area (34)  26  8 (23.5)  χ2= 0.826  0.363 
UL (46)  35  11 (23.9)  Fisher  0.197 
Trunk (37)  25  12 (32.4)  Fisher  0.338 
LL (52)  39  13 (25)  Fisher  0.073 
Duration of AD (years)Mean  7,3  4.5  MW-U= 1540.007
SD  4,2  3.6 
Median  3.2     
Age at AD onset (years)Mean  2,7  2.3  MW-U =2740.720
SD  2,8  2.5 
Median     

y, years; UL, Upper Limbs; LL, Lower Limbs; SD, Standard Deviation; χ2,Chi-square; MW-U, Mann-Whitney.

a

Other atopic diseases (in addition to AD).

Other atopic diseases were present in 45 patients (83.3%), and there was a family history of atopy in 35 patients (64.8%).

Regarding AD severity, most patients had mild and moderate EASI (35.2% and 46.3%, respectively). Nine (16.7%) had severe disease, and there was only one with very severe AD. The most affected body areas were: lower limbs (96.3%), upper limbs (85.2%), trunk (68.5%), face and cervical area (63%). Dermatitis affected three or more areas in 42 patients (78%).

Twenty 96 -h positive reactions were recorded in the 54 tested patients, that is a sensitization rate of 37.07% was found (20/54). The relevance index was 75%; that is, in 15 patients the current exposure to the sensitizer accounted for the current clinical picture. Therefore, the prevalence of ACD in the present sample was 27.7% (15/54; Tables 2 and 3).

Table 3.

Allergen profile: positive tests in relation to sex and age groups.

Allergens  PPT  p-value  4–9 y  10–18 y  p-value  Clinical relevance 
  n = 20 (%)  n = 19 (%)  n = 35 (%)    n = 31 (%)  n = 23 (%)     
Nickel sulfate  9 (16.7)  9 (25.7)  0.019  7 (22.6)  2 (8.7)  0.273  Yes 
Disperse blue  3 (5.6)  2 (10.5)  1 (2.8)  0.280  3 (9.7)  0.253  Yes 
FM I  3 (5.6)  3 (8.6)  0.544  2 (6.4)  1 (4.3)  1.000  Yes 
Neomycin  2 (3.7)  2 (5.7)  0.535  2 (6.4)  0.502  Yes 
Formaldehyde  1 (1.9)  1 (2.8)  1.000  1 (3.2)  1.000  No 
FM II  1 (1.9)  1 (2.8)  1.000  1 (4.3)  0.426  Yes 
MCI/MI  1 (1.9)  1 (2.8)  1.000  1 (3.2)  1.000  No 

PPT, Number of Positive Patch Tests; M, Male; F, Female; y, years; FMI, Fragrance Mix I; FM II; Fragrance mix II; MCI/MI, Methylchloroisothiazolinone/Methylisothiazolinone.

OBS: Other battery allergens, all of them with negative results: Tiuram mix, Colophony, Mercaptobenzothiazole, Sesquiterpene Lactone Mix, Lyral, P-tert-butylphenol formaldehyde resin, Potassium bichromate, Lanoline alcohol, - P-phenylenediamine, Composite mix, Hydrocortisone acetate, Budesonide, Methyldibromo glutaronitrile.

It was verified that 11 of the 31 children (35.5%) and 4 of the 23 adolescents (17.4%) had positive tests, but this difference did not reach statistical significance (p = 0.107). Similarly, the statistical tests did not show greater sensitization associated with the following variables: phototype, personal or family history of atopy, age at AD onset, location, and severity of the disease. The female sex showed a statistical trend towards more positive tests (p = 0.077). A shorter duration of AD (mean = 4.5 years; SD = 3.60 [median 3.2 years]) was associated with a higher frequency of positive tests when compared with a longer duration of AD (mean = 7.3 years, SD = 4.25 [median 6 years]), with p = 0.007 (Table 2).

The allergens with the highest frequency of sensitization were: nickel sulfate (16.7%), disperse blue (5.6%), and fragrance mix I (5.6%). The overall profile of the allergens is shown in the table (Table 3). No allergens were associated with a specific age group; however, an association was demonstrated between nickel sensitization and the female sex (p = 0.19; Table 3).

The “angry back syndrome” was detected in one child. Irritant reactions appeared in 11 patients (20.4%), 10 of which were children (between 4 and 9 years old). Fragrances and nickel were the most common irritating substances among children. There were no adolescents with occupational exposure and only one, aged 16 years, showed an irritative reaction (to fragrance mix II).

Discussion

The relationship between AD and ACD is yet to be fully understood.1,5,20

The Pediatric Contact Dermatitis Registry (PCDR), which contains data from the largest number of pediatric PTs in the US, reported that among 49% of children referred with AD, 42% also had ACD.2

Overall, most authors have not found significant differences in the prevalence of ACD between atopic and non-atopic children and adolescents.2,4,8,13,15,21–23 However, many of the published studies have shown controversial results regarding the subject. Sensitization rates varied considerably, as well as the study design in relation to sample size and characteristics, diagnostic criteria for AD, PT methodology, and allergens used. Additionally, a selection bias may have occurred in most studies because children without AD were more often referred for testing due to suspected ACD, whereas those with AD may have been referred because of AD recurrence.1 Few authors have published the PT results and the profile of children and adolescents with AD.2,3,6,14,24–35

Regardless of the fact that children with AD have an increased risk of sensitization in comparison to others, ACD can coexist in up to 30% of children with AD, according to recent publications.1,2,11

The batteries used in pediatric PT studies show geographic variations in allergen selection, but most are from North America and Europe.1,5,7 This is the first Brazilian study to assess the prevalence and profile of ACD in children and adolescents with AD through PT with a pediatric battery. In this sample, the prevalence of ACD was 27.7%, coinciding with the latest reviews of the international literature, in which the prevalence ranged from 20% to 44% in this group.1,5,7 Other Brazilian authors found a similar prevalence to the present one, in non-extensive, regionalized samples, but using the tests of the Brazilian standard battery (30 substances), not with a pediatric battery.13–15

Some studies have found a high rate of tests with irritant (false-positive) reactions in AD patients, probably due to a lower irritability threshold in a defective skin barrier.5,9,14,36 In the present study, irritative reactions also appeared, in 20.4% of children, mainly to nickel and fragrances, in the younger age group. However, although false-positive reactions are frequent in AD patients, weak positive reactions may occur and should be considered true positive ones, especially in patients with AD exacerbation.20 Moreover, many patients also had relevant weak positive reactions, as in a Brazilian pediatric study that reported 84.2% of relevant positive PTs with 1+ intensity reactions.15

In the present study, 57.4% of the sample were children between 4 and 9 years of age, and although it is not significant, more positive results were found in this younger age group. This finding is in accordance with other authors reports of high sensitization rates in children from younger age groups.2,4,31 On the other hand, as allergen exposure increases with age, more cases of ACD were reported in the group of adolescents in several studies.7,13,15 Additionally, in relation to age, significant differences are described with some allergens.7 A large US study reported that younger children were more sensitized to ingredients in personal hygiene products, while sensitization to disperse blue and gold was more common in older children.26

In the present sample, the age of AD onset in children with positive PTs did not differ statistically from those with negative PTs, in line with the findings of Labadie et al.31 Likewise, the present study found no association between phototype and more positive PTs (p = 0.361). Few studies have included this variable, and one has suggested that ethnic and cultural trends, such as body piercing, could influence the incidence of ACD.26

Similar to several studies, the present investigation also observed a higher number of referred female patients (64.8%) and a greater tendency towards positive PTs (p = 0.077).2,13,15,21,26

In the present study, a shorter duration of AD (median 3.2 years) was associated with more positive tests than a longer duration. This may be due to the predominance of referred younger children (57.4% of those aged between 4 and 9 years). The largest North American pediatric study also found more positive PTs in those with dermatitis of shorter duration.26

The association between the presence of other atopic diseases or family history and greater sensitization was not observed in the present sample. Other studies did not report any significant differences between atopy and age groups with positive PTs.7,8,25

Most of the patients in the present study had AD lesions in more than two body regions, as in the study by Rodrigues et al.15 Other authors have also reported more diffuse (spread) dermatitis among the tested children.2,7

Significant associations have been described between AD, ACD, and hand eczema in adolescents.1,9,35

In the present study, as there were more patients with mild to moderate AD, there was no possible correlation between higher disease severity and greater allergic sensitization. Similarly, Ozceker et al. did not find more ACD in children with severe AD.27 However, other authors have reported an association between more positive PTs and more severe disease.3,32,34

In fact, some studies have suggested that the sensitization threshold would be inversely related to AD severity. A lower positivity in PT reactions in patients with severe AD could be explained by the increase in T helper 2 (Th2) cells, as opposed to the deviation of Th1 cells from the immune system, traditionally observed in ACD.9,10,30

Allergen sensitization profile

The results of studies on the prevalence of ACD and the frequency of sensitizing allergens in children and adolescents with AD showed variations according to the selected sample, exposure time, type, and amount of tested substances.5,7,37

It is important to emphasize that there are differences in the allergen selection of the PT batteries used in pediatric studies worldwide;7 however, the most frequently applied are those of the North American Contact Dermatitis Group (NACDG)21 and the Pediatric Contact Dermatitis Registry (PCDR).26 Many studies in Europe have used standard or regional batteries according to the European Surveillance System on Contact Allergies (ESSCA).38,39

Recently, based on a consensus survey, the American Contact Dermatitis Society proposed a pediatric battery for children aged 6 to 18 years.39,40

However, these proposed batteries are not specifically targeted at children with AD. The allergen sensitization profile seems to be different in this population.3,5,11,23

In the present study, all AD patients were tested with a pediatric battery, following the recommendations of the EAACI,12 but adapted to the Brazilian reality (substitution of three substances). The allergens with the highest sensitization rates, in order of frequency, were: nickel sulfate, disperse blue, fragrance mix I, and neomycin.

A recent US publication on ACD in children highlighted the main allergens in those with AD: nickel, fragrance mix I, Balsam of Peru, bacitracin, lanolin, formaldehyde, and neomycin.2

Teo et al. (2019), in an extensive review of studies comparing ACD in individuals without AD and with AD, highlighted the ten most common allergens in the latter: nickel, fragrance mix I, methylisothiazolinone (MI), cobalt, colophony, neomycin, p-phenylenediamine (PPD) thiuram mix, balsam of Peru, and sodium metabisulfite.37 Three of these allergens (nickel, fragrances and neomycin) were also the most frequently found in the present study.

Patients with AD may be at increased risk of sensitization due to a defective barrier and frequent use of topical products (skincare and medications).2,9,2,37 Additionally, a large multicenter study (comprising 11 European countries) suggested that children with recalcitrant AD should also be tested for metals, disperse dyes, and Compositae.38

As found in several publications, in the present study, nickel was also the most sensitizing allergen5,14,26,28,29,31 and the most frequently associated with the female sex (p = 0.019).8,11,13,31,33 Nickel sensitization has been related to the habit of ear piercing. Toys, clothing (zippers, buttons, etc.), electronic equipment (tablets and cell phones) are continuous sources of nickel release.8,11

Disperse blue dye was the second most frequent allergen in the present study. Disperse dyes, present in brightly colored clothes and in some children's cosmetics, are potential allergens in children.6,12 Although such substances are not part of the Brazilian standard battery, their importance in children with AD has been mentioned in recent studies.22,25,26

Emollients are the main skincare products used in the treatment of AD. Contact dermatitis to fragrances and preservatives contained in these emollients may play a role in aggravating the disease.1,3,11,12 Fragrance mix I and II were found, in order of frequency, as the third and fifth allergens, respectively, in the present study. Fragrances are among the main substances present in toys and other scented products aimed at children, even in those labeled “fragrance-free”, which may contain related ingredients.26

Neomycin, the fourth most frequent allergen in the present study, is an antibiotic that is widely present in topical preparations and medications and has long been among the top allergens in children.11,21,25

Individuals with AD may be more sensitized to preservatives.37 Sensitization to methylchloroisothiazolinone, methylisothiazolinone, and the MCI/MI association present in cosmetics, cleaning and hygiene products has been increasing in recent studies.8,28 Formaldehyde and formaldehyde releasers are also common preservatives in everyday products11 and are among the top five allergens in a large pediatric AD study.2 However, in the present study, only one patient showed sensitization to formaldehyde and one to the MCI/MI association.

Although several authors have mentioned allergy to topical corticosteroids, mainly in patients with treatment-resistant AD, the present sample did not show positive tests to less potent corticosteroids (group A) present in the pediatric battery. Some studies attribute this negative result to the fact that patients with the recalcitrant disease more frequently use the higher potency corticosteroids (groups B and D).10

Considering that certain allergens seem to show specific patterns according to age,7,21,26 some authors suggest the use of PTs with different batteries aimed at children and adolescents:28 reduced batteries in children (due to smaller body surface area)4,6,25,29 and extended batteries in adolescents (greater exposure, including occupational).28,40

However, the authors agree on the difficulty of designing a battery of ideal substances to be used in the screening of the pediatric population and recommend the use of regional and substance-customized batteries from products used by the patients based on exposure history and clinical relevance.5,28,39,40

The strength of this study is that it is the first one in Brazil (to the best of our knowledge) to perform patch tests in children with AD using a pediatric battery to assess the prevalence, sensitizer, and ACD profile in this vulnerable group. The main limitations of this research could be the sample size, lack of a control group to be tested with the Brazilian standard battery to compare with other studies, and the fact that these patients came from a public health service (socioeconomic influences on exposure to certain allergens ). As this is a study that opens up the discussion on the use of pediatric batteries in recalcitrant atopic dermatitis, the cross-sectional design is the design that corresponds to the objectives.

Conclusions

ACD can coexist and play a role in the worsening of AD. Almost one-third of children and adolescents with AD in a southern Brazilian sample attended in the public health system were diagnosed with ACD, using a pediatric patch test battery. The most important allergens in this population were nickel sulfate, disperse blue, fragrances, and neomycin. Future multicenter studies with larger samples, control groups, and standardized methodologies are required.

The present study adds information about sensitizers in children and adolescents with recalcitrant AD.

Financial support

None declared.

Authors’ contributions

Cristiane Almeida Soares Cattani: Statistical analysis; approval of the final version of the manuscript; design and planning of the study; drafting and editing of the manuscript; collection, analysis, and interpretation of data; effective participation in research orientation; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases; critical review of the literature; critical review of the manuscript.

Renan Rangel Bonamigo: Statistical analysis; approval of the final version of the manuscript; design and planning of the study; drafting and editing of the manuscript; collection, analysis, and interpretation of data; effective participation in research orientation; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases; critical review of the literature; critical review of the manuscript.

Kenselyn Oppermann: Approval of the final version of the manuscript; collection, analysis, and interpretation of data; effective participation in research orientation; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases; critical review of the literature.

Simone Perazzoli: Approval of the final version of the manuscript; collection, analysis, and interpretation of data; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases; critical review of the literature.

Nathalia Hoffmann Guarda: Approval of the final version of the manuscript; collection, analysis, and interpretation of data; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases; critical review of the literature.

Paula Baréa: Approval of the final version of the manuscript; collection, analysis, and interpretation of data; intellectual participation in the propaedeutic and/or therapeutic conduct of the studied cases; critical review of the literature.

Conflicts of interest

None declared.

Acknowledgments

The authors would like to thank IPI-ASAC Brasil for donating the pediatric battery of tests used in this study.

References
[1]
A.B. Simonsen, J.D. Johansen, M. Deleuran, C.G. Mortz, M. Sommerlund.
Contact allergy in children with atopic dermatitis: a systematic review.
Br J Dermatol, 177 (2017), pp. 395-405
[2]
S.E. Jacob, M. McGowan, N.B. Silverberg, J.L. Pelletier, L. Fonacier, N. Mousdicas, et al.
Pediatric Contact Dermatitis Registry Data on Contact Allergy in Children With Atopic Dermatitis.
JAMA Dermatol, 153 (2017), pp. 765-770
[3]
A.B. Simonsen, J.D. Johansen, M. Deleuran, C.G. Mortz, L. Skov, M. Sommerlund.
Children with atopic dermatitis may have unacknowledged contact allergies contributing to their skin symptoms.
J Eur Acad Dermatol Venereol, 32 (2018), pp. 428-436
[4]
A.B. Fortina, I. Romano, A. Peserico, L.F. Eichenfield.
Contact sensitization in very young children.
J Am Acad Dermatol., 65 (2011), pp. 772-779
[5]
J. Borok, C. Matiz, A. Goldenberg, S.E. Jacob.
Contact Dermatitis in Atopic Dermatitis Children-Past, Present, and Future.
Clin Rev in Allergy Immunol, 56 (2019), pp. 86-98
[6]
S.E. Jacob, A. Yang, E. Herro, C. Zhang.
Contact allergens in a pediatric population: association with atopic dermatitis and comparison with other north american referral centers.
J Clin Aesthet Dermatol, 3 (2010), pp. 29-35
[7]
D.F. Rodrigues, E.M.A. Goulart.
Patch-test results in children and adolescents: systematic review of a 15-year period.
An Bras Dermatol, 91 (2016), pp. 64-72
[8]
Y. Zafrir, A. Trattner, E. Hodak, O. Eldar, M. Lapidoth, D.B. Amitai.
Patch testing in Israeli children with suspected allergic contact dermatitis: A retrospective study and literature review.
Pediatr Dermatol, 35 (2018), pp. 76-86
[9]
J.P. Thyssen, J.P. McFadden, I. Kimber.
The multiple factors affecting the association between atopic dermatitis and contact sensitization.
Allergy, 69 (2014), pp. 28-36
[10]
M. Boonstra, T. Rustemeyer, M.A. Middelkamp-Hup.
Both children and adult patients with difficult-to-treat atopic dermatitis have high prevalences of concomitant allergic contact dermatitis and are frequently polysensitized.
J Eur Acad Dermatol Venereol, 32 (2018), pp. 1554-1561
[11]
H. Neale, A.C. Garza-Mayers, I. Tam, J. Yu.
Pediatric allergic contact dermatitis. Part I: Clinical features and common contact allergens in children.
J Am Acad Dermatol, 84 (2021), pp. 235-244
[12]
F.B.W. Spek, U. Darsow, C.G. Mortz, D. Orton, M. Worm, A. Muraro, et al.
EAACI position paper for practical patch testing in allergic contact dermatitis in children.
Pediatr Allergy Immunol, 26 (2015), pp. 598-606
[13]
I. Duarte, R. Lazzarini, C.M. Kobata.
Contact Dermatitis in Adolescents.
Am J Contact Dermat, 14 (2003), pp. 200-202
[14]
C.M. Kobata.
Testes de contato em crianças com eczema. Rio de Janeiro. Dissertação [Mestrado em Dermatologia] - USP.
(2010),
[15]
D.F. Rodrigues, E.M.A. Goulart.
Patch test results in children and adolescents. Study from the Santa Casa de Belo Horizonte Dermatology Clinic, Brazil, from 2003 to 2010.
An Bras Dermatol, 90 (2015), pp. 671-683
[16]
L.F. Eichenfield, J.M. Hanifin, T.A. Luger, S.R. Stevens, H.B. Pride.
Consensus conference on pediatric atopic dermatitis.
J Am Acad Dermatol, 49 (2003), pp. 1088-1095
[17]
Y.A. Leshem, T. Hajar, J.M. Hanifin, E.L. Simpson.
What the Eczema Area and Severity Index score tells us about the severity of atopic dermatitis: an interpretability study.
Br J Dermatol, 172 (2015), pp. 1353-1357
[18]
ipi.brasil.com [Internet]. Brasil: IPI ASAC Brasil; c2020 [cited 2021 Jan 10]. Available from: https://ipibrasil.com.br/teste-de-contato-patch-test/.
[19]
I.A.G. Duarte, G.M. Tanaka, N.M. Suzuki, R. Lazzarini, A.S.A. Lopes, B.M.F. Volpini, et al.
Patch test standard series recommended by the Brazilian Contact Dermatitis Study Group during the 2006-2011 period.
An Bras Dermatol, 88 (2013), pp. 1015-1018
[20]
J.L. Owen, P.P. Vakharia, J.I. Silverberg.
The Role and Diagnosis of Allergic Contact Dermatitis in Patients with Atopic Dermatitis.
Am J Clin Dermatol, 19 (2018), pp. 293-302
[21]
K.A. Zug, A.K. Pham, D.V. Belsito, J.G. Dekoven, V.A. DeLeo, J.F. Fowley Jr., et al.
Patch testing in children from 2005 to 2012: results from the North American contact dermatitis group.
Dermatitis, 25 (2014), pp. 345-355
[22]
A.B. Fortina, E. Fontana, A. Peserico.
Contact Sensitization in Children: A Retrospective Study of 2,614 Children from a Single Center.
Pediatr Dermatol, 33 (2016), pp. 399-404
[23]
S. Lubbes, T. Rustemeyer, J.H.S. Smitt, M.L. Schuttelaar, M.A. Middelkamp-Hup.
Contact sensitization in Dutch children and adolescents with and without atopic dermatitis – a retrospective analysis.
Contact Dermatitis, 76 (2017), pp. 151-159
[24]
A. Akan, M. Toyran, E. Vezir, D. Azkur, A. Kaya, M. Erkoçoğlu, et al.
The patterns and clinical relevance of contact allergen sensitization in a pediatric population with atopic dermatitis.
Turk J Med Sci, 45 (2015), pp. 1207-1213
[25]
M. Ascha, M. Irfan, J. Bena, J.S. Taylor, A. Sood.
Pediatric patch testing: A 10-year retrospective study.
Ann Allergy Asthma Immunol, 117 (2016), pp. 661-667
[26]
A. Goldenberg, N. Mousdicas, N. Silverberg, D. Powell, J.L. Pelletier, J.I. Silverberg, et al.
Pediatric Contact Dermatitis Registry Inaugural Case Data.
Dermatitis, 27 (2016), pp. 293-302
[27]
D. Ozceker, F. Haslak, F. Dilek, S. Sipahi, E. Yucel, N. Guler, et al.
Contact sensitization in children with atopic dermatitis.
Allergol Immunopathol (Madr), 47 (2019), pp. 47-51
[28]
W. Francuzik, J. Geier, S. Schubert, M. Worm.
A case-control analysis of skin contact allergy in children and adolescents.
Pediatr Allergy Immunol, 30 (2019), pp. 632-637
[29]
C. Felmingham, R. Davenport, H. Bala, A. Palmer, R. Nixon.
Allergic contact dermatitis in children and proposal for an Australian Paediatric Baseline Series.
Australas J Dermatol, 61 (2020), pp. 33-38
[30]
M. Uehara, T. Sawai.
A Longitudinal Study of Contact Sensitivity in Patients With Atopic Dermatitis.
Arch Dermatol, 125 (1989), pp. 366-368
[31]
F. Giordano-Labadie, F. Rancé, F. Pellegrin, J. Bazex, G. Dutau, H.P. Schwarze.
Frequency of contact allergy in children with atopic dermatitis: results of a prospective study of 137 cases.
Contact Dermatitis, 40 (1999), pp. 192-195
[32]
C. Mailhol, V. Lauwers-Cances, F. Rancé, C. Paul, F. Giordano-Labadie.
Prevalence and risk factors for allergic contact dermatitis to topical treatment in atopic dermatitis: a study in 641 children.
[33]
E. Czarnobilska, K. Obtulowicz, W. Dyga, R. Spiewak.
The most important contact sensitizers in Polish children and adolescents with atopy and chronic recurrent eczema as detected with the extended European Baseline Series.
Pediatr Allergy Immunol, 22 (2011), pp. 252-256
[34]
E.M. Herro, C. Matiz, K. Sullivan, C. Hamann, S.E. Jacob.
Frequency of contact allergens in pediatric patients with atopic dermatitis.
J Clin Aesthet Dermatol, 4 (2011), pp. 39-41
[35]
M. Isaksson, S. Olhardt, J. Rådehed, Å. Svensson.
Children with atopic dermatitis should always be patch-tested if they have hand or foot dermatitis.
Acta Derm Venereol, 95 (2015), pp. 583-586
[36]
P.A. Klas, G. Corey, F.J. Storrs, S.C. Chan, J.M. Hanifin.
Allergic and irritant patch test reactions and atopic disease.
Contact Dermatitis, 34 (1996), pp. 121-124
[37]
Y. Teo, J.P. McFadden, I.R. White, M. Lynch, P. Banerjee.
Allergic contact dermatitis in atopic individuals: Results of a 30-year retrospective study.
Contact Dermatitis, 81 (2019), pp. 409-416
[38]
A.B. Fortina, S.M. Cooper, R. Spiewak, E. Fontana, A. Schnuch, W. Uter.
Patch test results in children and adolescents across Europe. Analysis of the ESSCA Network 2002-2010.
Pediatr Allergy Immunol, 26 (2015), pp. 446-455
[39]
J. Yu, A.R. Atwater, B. Brod, J.K. Chen, S.S. Chisolm, D.E. Cohen, et al.
Pediatric Baseline Patch Test Series: Pediatric Contact Dermatitis Workgroup.
Dermatitis, 29 (2018), pp. 206-212
[40]
J.M. Tran, A.R. Atwater, M. Reeder.
Patch testing in children: not just little adults.
Cutis., 104 (2019), pp. 288-290

Study conducted at the Sanitary Dermatology Outpatient Clinic, Porto Alegre, RS, Brazil.

Copyright © 2022. Sociedade Brasileira de Dermatologia
Idiomas
Anais Brasileiros de Dermatologia (Portuguese)

Receba a nossa Newsletter

Opções de artigo
Ferramentas
en pt
Cookies policy Política de cookies
To improve our services and products, we use "cookies" (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here. Utilizamos cookies próprios e de terceiros para melhorar nossos serviços e mostrar publicidade relacionada às suas preferências, analisando seus hábitos de navegação. Se continuar a navegar, consideramos que aceita o seu uso. Você pode alterar a configuração ou obter mais informações aqui.