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Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020 6
INTRODUCTION
A
topic dermatitis (AD) is a pruritic inflammatory
dermatosis with a genetic predisposition that
evolves by recurrent flare-ups affecting mainly
infants and small children.[1]
Worldwide, its prevalence
has doubled or tripled over the past 30 years.[2]
InAfrica,
the disease is increasingly reported.[3-5]
Although AD
is not lethal, it can result in significant morbidity and
societal cost.[6]
Thus, AD is now a real public health
problem. In Parakou, in the north of Benin, no data
on AD were known. The aim of this study was to
determine the epidemiological and clinical profile of
atopic dermatitis (AD) in children in Parakou, Benin.
A preliminary census of all cases of AD received in
the dermatology-venereology department at Borgou-
Alibori CHU in Parakou (Benin) since its creation
(from January 2009 to December 2017, i.e., 8 years)
concluded that the hospital incidence was 1.6%,[7]
and
led us to carry out the study in the general population.
MATERIALS AND METHODS
This was a transversal descriptive and analytical study that
took place from April 30 to July 28, 2018. It was conducted
in thirty neighborhoods/villages of the township of Parakou,
capital of the Department of Borgou in the Republic of
Benin. Children aged 0–15 years at the time of the survey
RESEARCH ARTICLE
Epidemio-clinical Profile of Atopic Dermatitis in
Children in General Population in Parakou (Benin)
Nadège Agbessi1
, Fabrice Akpadjan2
, Bérénice Dégboé2
, Gloria Nouhoumon1
,
Christiane Koudoukpo1
, Hugues Adegbidi2
, Félix Atadokpédé2
1
Department of Dermatology-Venereology, Faculty of Medicine of Parakou, University of Parakou, Benin,
2
Department of Dermatology-Venereology, Faculty of Health Sciences of Cotonou, University of Abomey-Calavi,
Benin
ABSTRACT
Introduction: The aim of this study was to determine the epidemiological and clinical profile of atopic dermatitis (AD)
in children in Parakou (Benin). Materials and Methods: This was a cross-sectional, descriptive, and analytical study
of children aged 0–15 years old, selected after a two-stage cluster survey carried out. The diagnosis of AD was laid the
basis of the criteria of the working group of the United Kingdom (UKWP). Data were analyzed with the Epi-info version
3.5.1. Results: A total of 157 children with AD were selected between 2160 (7.27%). Their mean age was 4.74 ± 4.33
years old. The sex ratio was 1.57 and the majority of children (80.25%) were doing their pushes regardless of the climatic
season. The predominant elemental lesions were erythema (91.97%), crusts, erosions (74.45%), and vesicles (40.88%).
Some children had at least two lesions. The most recognized minor signs of atopy were cutaneous xerosis (91.97%) and
Dennie-Morgan sign (76.64%). Lesions were predominant in the retroauricular folds (41.61%). The dominant clinical forms
were vulgar eczema (48.18%), lichenified forms (32.85%), and impetiginized forms (24.09%). According to the Scoring
Atopic Dermatitis (SCORAD), 67.15% had moderate AD. Conclusion: The frequency of AD in children in Parakou is not
negligible and the clinical manifestations are varied.
Key words: Epidemiology, Clinical, Atopic dermatitis, Children, Parakou
Address for correspondence: Fabrice Akpadjan, Department of Dermatology, Venereology, National Hospital and
University Centre of Cotonou, Faculty of Health Sciences, 09BP: 441 Cotonou, Benin
https://doi.org/10.33309/2639-8524.030102 www.asclepiusopen.com
© 2020 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.
Agbessi: Atopic dermatitis in children in Parakou (Benin)
 Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020
were included in the study, selected after a two-stage cluster
survey. The minimum sample size was determined using the
Schwartz formula. The diagnosis of AD was selected on the
basis of the UKWP diagnostic criteria:
An itchy skin condition (or parental report of scratching or
rubbing in a child)
Plus three or more of the following
1.	 History of involvement of the skin creases such as folds
of elbows, behind the knees, fronts of ankles, or around
the neck (including cheeks in children under 10).
2.	 A personal history of asthma or hay fever (or history of
atopic disease in a 1st
-degree relative in children under 4).
3.	 A history of a general dry skin in the last year.
4.	 Visible flexural eczema (or eczema involving the cheeks/
forehead and outer limbs in children under 4).
5.	 Onset under the age of 2 (not used if child is under 4).
Clinical and epidemiological data were collected using a pre-
established and pre-validated questionnaire in two villages
in the township of Tchaourou not included in this study. All
children were examined by a dermatologist. The data were
entered using Epi data 3.5.1 software and analyzed using Epi-
info version 3.5.1 software.
RESULTS
A total of 157 children with AD were diagnosed among 2160
interviewed and examined, a prevalence of 7.27% (95%
CI of 6.23–8.42). Their average age was 4.74 ± 4.33 years
with a sex ratio of 1.57 (96 males to 61 females). Most of
the children (80.25%) had relapses regardless of the climatic
season (dry or rainy).
Among the 157 children, the physical exam was abnormal in
137 children, that is, 87.26%, with four having generalized
pruritic dermatosis and 133 having localized pruritic
dermatosis [Figure 1]. Erythema (91.97%), and scabs and
erosions (74.45%) were the predominant primary lesions
[Table 1]. The minor signs of atopy noted in these 137
children were cutaneous xerosis (91.97%) and Dennie-
Morgan’s sign (76.64%). No white demography was noted
[Table 2].
Retro auricular groove was the predominant site (41.61%),
followed by the elbow fold (25.55%).
•	 Before the age of 2 years (n=46), the top 5 sites were
retroauricular groove (18.98%); forehead (13.14%);
cheeks (12.41%); elbow folds (10.22%); neck (8.76%);
arm (8.76%); and forearm (7.30%).
•	 After 2 years (n=91), the first 5 sites are the retroauricular
grooves (22.63%); the feet (17.52%); the elbow folds
(15.33%); the axillary regions (14.60%); and the
buttocks (13.87%).
Table 2: Different stigmas of atopy noticed
Minor signs (n=137) Number Percentage
White demography 0 0.00
Cheilitis 2 1.46
Ichthyosis 2 1.46
Achromians eczematides 3 2.19
Periorbital hyperpigmentation 4 2.92
None 4 2.92
Palmoplantar hyperlinearity 9 6.57
Low hair implantation 9 6.57
Simple follicular keratosis 25 18.25
Retroauricular cracks 50 36.50
Dennie-Morgan’s sign 105 76.64
Xerosis 126 91.97
Table 1: Different objectified elementary lesions
Elementary lesions (n =137) Number Percentage
Cracks 2 1.46
Pustules 8 5.84
Papules 12 8.76
Edema 13 9.49
Excoriations 18 13.14
Scales 23 16.79
Oozing vesicles 54 39.42
Non oozing vesicles 58 42.34
Scabs and erosions 102 74.45
Erythema 126 91.97
Figure 1: Localized dermatosis on the wrist and back of the
hand vesicles + erosions
Lichenification was the leading complication [Table 3]
(32.85%), followed by impetiginization (24.09%) [Figure 2].
Eczema vulgaris (48.18%) was the predominant clinical
Agbessi: Atopic dermatitis in children in Parakou (Benin)
Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020 8
form [Table 4], followed by lichenified (32.85%) and
impetiginized (24.09%) forms. According to the AD severity
score (SCORAD), 41 children (29.93%) had mild AD, 92
(67.15%) had moderate AD, and 4 (2.92%) had severe AD.
DISCUSSION
The main limitation of this study is inherent to the fact that
allergological tests are not carried out due to the lack of
access to reagents.
The prevalence of AD determined by our study is close to
that found in Marrakech in 2015.[8]
The one found in 2009
in Cotonou[4]
is lower than ours (5.5%). However, it is much
lower than those found in studies conducted in Yaoundé[9]
and
Togo.[10]
This variability in results could be explained by the
different methodologies adopted and the study populations.
The average age of children with AD (4.74 ± 4.33 years) was
similar to that found in Lomé in 2015[10]
and Marrakech in
2015.[8]
However, it is different from that found in Cotonou in
2009,[4]
who reported an average age of 247.2 months (20.6
years). This difference could be related to the choice of age
groups in the conduct of epidemiological studies on AD.
Male predominance was noted in the present study as well
as in the Maghreb and Moroccan series.[8,11]
In contrast, the
studies in Cameroon,[9]
Togo (Lome),[10]
and Cotonou (Benin)
noted female predominance. This significant difference with
the results of these three studies could be related to the action
of certain factors considered to protect or promote atopic risk
influenced by gender as suggested by Hagendorens et al.[12]
A total of 61.15% of children began the disease before the
age of 2 years. An onset before the age of 2 years in all
sick children (100%) was also noticed in Marrakech.[8]
In
Cotonou, on the other hand, in 2009, only 25.7% of patients
started the AD before the age of two.[4]
Erythema (91.97%) and scabs and erosions (74.45%) were the
predominant basic lesions. These results are similar to those
found in Cotonou in 2009[4]
as concerns xerosis (90%) and
scabs and erosions (67.65%). However, erythema was present
in only 50% of their patients. Furthermore, the presence of
erythema was noted in 78.6% of patients in Marrakech in
2015,[8]
but scabs and erosions were less frequent in their
context (35.7%). This proportion of erythema found by the
present study compared to the study conducted in Cotonou
calls into question the difficulty of assessing (in defect or
excess) erythema on black skin.
The site of lesions varied according to age in our study.
Before the age of 2 years, the predominant site was the
retroauricular groove, followed by the forehead and cheeks.
The same observation was made in Marrakech in 2015.[8]
On the other hand, Atadokpédé et al.[4]
found that the limbs
were the predominant site at this age. After 2 years, the
predominant site was the retroauricular groove, followed by
the feet and elbow folds. In Marrakech in 2015, Baino et al.[8]
found 100% localization in the cheeks at this age.
CONCLUSION
This study allowed us to observe that AD is a reality among
children in Parakou in the north of Benin and that it should
not be neglected. Contrary to the study carried out in the south
Table 4: Clinical forms
Clinical forms (n=137) Number Percentage
Nummular eczema 0 0.00
Juvenile dermatitis plantar 0 0.00
Nipple eczema 0 0.00
Prurigo of Besnier 1 0.73
Atopic cheilitis 2 1.46
Erythrodermal eczema 4 2.92
Dysidrosic eczema 4 2.92
Impetiginized eczema 33 24.09
Lichenified eczema 45 32.85
Eczema vulgar 66 48.18
Table 3: Various complications observed
Complications (C) (n=137) Number Percentage
Growth retardation 0 0.00
Ophthalmology 0 0.00
Psychic impact 1 0.73
Contact dermatitis 2 1.46
Impetiginization 33 24.09
Lichenification 45 32.85
Figure 2: Lichenified and impetiginized eczema
Agbessi: Atopic dermatitis in children in Parakou (Benin)
9 Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020
of Benin (in Cotonou in 2009) in the hospital population, this
one had the merit of taking stock of the situation of AD in
the general pediatric population. A better knowledge of the
manifestations of AD would help physicians in general and
pediatricians in particular to better manage it. The majority
of these children do not come to the dermatologist’s office as
a first-line treatment; especially in our sub-Saharan African
countries where access to specialized care is still a luxury for
the most vulnerable populations.
REFERENCES
1.	 Dammak A, Guillet G. Atopic dermatitis in children. J Pediatr
Child Care 2011;24:84-102.
2.	 Catteau B. Atopic dermatitis: Epidemiology and current
clinical data. Rev Fr Allergol Immunol Clin 2002;42:373-7.
3.	 Kobangué L, Piamalé G, Bureau JJ, Sépou A. Epidemiological
and clinical aspects of atopic dermatitis at the National Hospital
and University Centre of Bangui. Ann Dermatol Venereol
2007;134 Suppl 1:S98.
4.	 Atadokpédé F, Adégbidi H, Koudoukpo C, Agbessi N,
Yedomon H, do-Ango-Padonou F, et al. Atopic dermatitis in
Cotonou, Benin: Clinical and therapeutic aspects. Dakar Med
2012;57:1-7.
5.	 Nnoruka EN. Current epidemiology of atopic dermatitis in
South-Eastern Nigeria. Int J Dermatol 2004 43:739-44.
6.	 Yu SH, Attarian H, Zee P, Silverberg JI. Burden of sleep
and fatigue in US adults with atopic dermatitis. Dermatitis
2016;27:50-8.
7.	 Koudoukpo C, Akpadjan F, Agbessi N, Dégboé B,
Nouhoumon G, Adégbidi H, et al. Epidemiological aspects
of atopic dermatitis in Borgou-Alibori Teaching Hospital of
Parakou (Benin). Health Sci Dis 2019;20:94-7.
8.	 BainoA, Hocar O,Akhdari N,Amal S. Prevalence and clinical-
epidemiological profile of dermatitis atopic in Morocco. Ann
Dermatol Venereol 2016;143 Suppl 1:S43-4.
9.	 Djénabou A. Atopic eczema in adolescents in Yaoundé,
Cameroon. Rev Fr Allergol 2017;57:265-83.
10.	 Técléssou JN, Mouhari-Toure A, Akakpo S, Bayaki S,
Boukari OB, Gnassingbe W, et al. Risk factors and allergic
manifestations associated with atopic dermatitis in Lomé
(Togo): A multicenter study of 476 children aged 0-15 years.
Méd Santé Trop 2016;26:88-91.
11.	 Baghou S, Bensaad D, Taieb A, Ammar-Khodja A. Prevalence
and clinical profile of atopic dermatitis in Algeria. Ann
Dermatol Venereol 2012;139:140.
12.	 Hagendorens MM, Bridts CH, Lauwers K. Perinatal risk
factors for sensitization, atopic dermatitis and wheezing
during the first year of life (PIPO study). Clin Exp Allergy
2005;35:733-40.
How to cite this article: Agbessi N, Akpadjan F,
Dégboé B, Nouhoumon G, Koudoukpo C, Adegbidi H,
Atadokpédé F. Epidemio-clinical Profile of Atopic
Dermatitis in Children in General Population in Parakou
(Benin). Clinic Res Dermatol 2020;3(1):6-9.

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Epidemio-clinical Profile of Atopic Dermatitis in Children in General Population in Parakou (Benin)

  • 1. Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020 6 INTRODUCTION A topic dermatitis (AD) is a pruritic inflammatory dermatosis with a genetic predisposition that evolves by recurrent flare-ups affecting mainly infants and small children.[1] Worldwide, its prevalence has doubled or tripled over the past 30 years.[2] InAfrica, the disease is increasingly reported.[3-5] Although AD is not lethal, it can result in significant morbidity and societal cost.[6] Thus, AD is now a real public health problem. In Parakou, in the north of Benin, no data on AD were known. The aim of this study was to determine the epidemiological and clinical profile of atopic dermatitis (AD) in children in Parakou, Benin. A preliminary census of all cases of AD received in the dermatology-venereology department at Borgou- Alibori CHU in Parakou (Benin) since its creation (from January 2009 to December 2017, i.e., 8 years) concluded that the hospital incidence was 1.6%,[7] and led us to carry out the study in the general population. MATERIALS AND METHODS This was a transversal descriptive and analytical study that took place from April 30 to July 28, 2018. It was conducted in thirty neighborhoods/villages of the township of Parakou, capital of the Department of Borgou in the Republic of Benin. Children aged 0–15 years at the time of the survey RESEARCH ARTICLE Epidemio-clinical Profile of Atopic Dermatitis in Children in General Population in Parakou (Benin) Nadège Agbessi1 , Fabrice Akpadjan2 , Bérénice Dégboé2 , Gloria Nouhoumon1 , Christiane Koudoukpo1 , Hugues Adegbidi2 , Félix Atadokpédé2 1 Department of Dermatology-Venereology, Faculty of Medicine of Parakou, University of Parakou, Benin, 2 Department of Dermatology-Venereology, Faculty of Health Sciences of Cotonou, University of Abomey-Calavi, Benin ABSTRACT Introduction: The aim of this study was to determine the epidemiological and clinical profile of atopic dermatitis (AD) in children in Parakou (Benin). Materials and Methods: This was a cross-sectional, descriptive, and analytical study of children aged 0–15 years old, selected after a two-stage cluster survey carried out. The diagnosis of AD was laid the basis of the criteria of the working group of the United Kingdom (UKWP). Data were analyzed with the Epi-info version 3.5.1. Results: A total of 157 children with AD were selected between 2160 (7.27%). Their mean age was 4.74 ± 4.33 years old. The sex ratio was 1.57 and the majority of children (80.25%) were doing their pushes regardless of the climatic season. The predominant elemental lesions were erythema (91.97%), crusts, erosions (74.45%), and vesicles (40.88%). Some children had at least two lesions. The most recognized minor signs of atopy were cutaneous xerosis (91.97%) and Dennie-Morgan sign (76.64%). Lesions were predominant in the retroauricular folds (41.61%). The dominant clinical forms were vulgar eczema (48.18%), lichenified forms (32.85%), and impetiginized forms (24.09%). According to the Scoring Atopic Dermatitis (SCORAD), 67.15% had moderate AD. Conclusion: The frequency of AD in children in Parakou is not negligible and the clinical manifestations are varied. Key words: Epidemiology, Clinical, Atopic dermatitis, Children, Parakou Address for correspondence: Fabrice Akpadjan, Department of Dermatology, Venereology, National Hospital and University Centre of Cotonou, Faculty of Health Sciences, 09BP: 441 Cotonou, Benin https://doi.org/10.33309/2639-8524.030102 www.asclepiusopen.com © 2020 The Author(s). This open access article is distributed under a Creative Commons Attribution (CC-BY) 4.0 license.
  • 2. Agbessi: Atopic dermatitis in children in Parakou (Benin) Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020 were included in the study, selected after a two-stage cluster survey. The minimum sample size was determined using the Schwartz formula. The diagnosis of AD was selected on the basis of the UKWP diagnostic criteria: An itchy skin condition (or parental report of scratching or rubbing in a child) Plus three or more of the following 1. History of involvement of the skin creases such as folds of elbows, behind the knees, fronts of ankles, or around the neck (including cheeks in children under 10). 2. A personal history of asthma or hay fever (or history of atopic disease in a 1st -degree relative in children under 4). 3. A history of a general dry skin in the last year. 4. Visible flexural eczema (or eczema involving the cheeks/ forehead and outer limbs in children under 4). 5. Onset under the age of 2 (not used if child is under 4). Clinical and epidemiological data were collected using a pre- established and pre-validated questionnaire in two villages in the township of Tchaourou not included in this study. All children were examined by a dermatologist. The data were entered using Epi data 3.5.1 software and analyzed using Epi- info version 3.5.1 software. RESULTS A total of 157 children with AD were diagnosed among 2160 interviewed and examined, a prevalence of 7.27% (95% CI of 6.23–8.42). Their average age was 4.74 ± 4.33 years with a sex ratio of 1.57 (96 males to 61 females). Most of the children (80.25%) had relapses regardless of the climatic season (dry or rainy). Among the 157 children, the physical exam was abnormal in 137 children, that is, 87.26%, with four having generalized pruritic dermatosis and 133 having localized pruritic dermatosis [Figure 1]. Erythema (91.97%), and scabs and erosions (74.45%) were the predominant primary lesions [Table 1]. The minor signs of atopy noted in these 137 children were cutaneous xerosis (91.97%) and Dennie- Morgan’s sign (76.64%). No white demography was noted [Table 2]. Retro auricular groove was the predominant site (41.61%), followed by the elbow fold (25.55%). • Before the age of 2 years (n=46), the top 5 sites were retroauricular groove (18.98%); forehead (13.14%); cheeks (12.41%); elbow folds (10.22%); neck (8.76%); arm (8.76%); and forearm (7.30%). • After 2 years (n=91), the first 5 sites are the retroauricular grooves (22.63%); the feet (17.52%); the elbow folds (15.33%); the axillary regions (14.60%); and the buttocks (13.87%). Table 2: Different stigmas of atopy noticed Minor signs (n=137) Number Percentage White demography 0 0.00 Cheilitis 2 1.46 Ichthyosis 2 1.46 Achromians eczematides 3 2.19 Periorbital hyperpigmentation 4 2.92 None 4 2.92 Palmoplantar hyperlinearity 9 6.57 Low hair implantation 9 6.57 Simple follicular keratosis 25 18.25 Retroauricular cracks 50 36.50 Dennie-Morgan’s sign 105 76.64 Xerosis 126 91.97 Table 1: Different objectified elementary lesions Elementary lesions (n =137) Number Percentage Cracks 2 1.46 Pustules 8 5.84 Papules 12 8.76 Edema 13 9.49 Excoriations 18 13.14 Scales 23 16.79 Oozing vesicles 54 39.42 Non oozing vesicles 58 42.34 Scabs and erosions 102 74.45 Erythema 126 91.97 Figure 1: Localized dermatosis on the wrist and back of the hand vesicles + erosions Lichenification was the leading complication [Table 3] (32.85%), followed by impetiginization (24.09%) [Figure 2]. Eczema vulgaris (48.18%) was the predominant clinical
  • 3. Agbessi: Atopic dermatitis in children in Parakou (Benin) Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020 8 form [Table 4], followed by lichenified (32.85%) and impetiginized (24.09%) forms. According to the AD severity score (SCORAD), 41 children (29.93%) had mild AD, 92 (67.15%) had moderate AD, and 4 (2.92%) had severe AD. DISCUSSION The main limitation of this study is inherent to the fact that allergological tests are not carried out due to the lack of access to reagents. The prevalence of AD determined by our study is close to that found in Marrakech in 2015.[8] The one found in 2009 in Cotonou[4] is lower than ours (5.5%). However, it is much lower than those found in studies conducted in Yaoundé[9] and Togo.[10] This variability in results could be explained by the different methodologies adopted and the study populations. The average age of children with AD (4.74 ± 4.33 years) was similar to that found in Lomé in 2015[10] and Marrakech in 2015.[8] However, it is different from that found in Cotonou in 2009,[4] who reported an average age of 247.2 months (20.6 years). This difference could be related to the choice of age groups in the conduct of epidemiological studies on AD. Male predominance was noted in the present study as well as in the Maghreb and Moroccan series.[8,11] In contrast, the studies in Cameroon,[9] Togo (Lome),[10] and Cotonou (Benin) noted female predominance. This significant difference with the results of these three studies could be related to the action of certain factors considered to protect or promote atopic risk influenced by gender as suggested by Hagendorens et al.[12] A total of 61.15% of children began the disease before the age of 2 years. An onset before the age of 2 years in all sick children (100%) was also noticed in Marrakech.[8] In Cotonou, on the other hand, in 2009, only 25.7% of patients started the AD before the age of two.[4] Erythema (91.97%) and scabs and erosions (74.45%) were the predominant basic lesions. These results are similar to those found in Cotonou in 2009[4] as concerns xerosis (90%) and scabs and erosions (67.65%). However, erythema was present in only 50% of their patients. Furthermore, the presence of erythema was noted in 78.6% of patients in Marrakech in 2015,[8] but scabs and erosions were less frequent in their context (35.7%). This proportion of erythema found by the present study compared to the study conducted in Cotonou calls into question the difficulty of assessing (in defect or excess) erythema on black skin. The site of lesions varied according to age in our study. Before the age of 2 years, the predominant site was the retroauricular groove, followed by the forehead and cheeks. The same observation was made in Marrakech in 2015.[8] On the other hand, Atadokpédé et al.[4] found that the limbs were the predominant site at this age. After 2 years, the predominant site was the retroauricular groove, followed by the feet and elbow folds. In Marrakech in 2015, Baino et al.[8] found 100% localization in the cheeks at this age. CONCLUSION This study allowed us to observe that AD is a reality among children in Parakou in the north of Benin and that it should not be neglected. Contrary to the study carried out in the south Table 4: Clinical forms Clinical forms (n=137) Number Percentage Nummular eczema 0 0.00 Juvenile dermatitis plantar 0 0.00 Nipple eczema 0 0.00 Prurigo of Besnier 1 0.73 Atopic cheilitis 2 1.46 Erythrodermal eczema 4 2.92 Dysidrosic eczema 4 2.92 Impetiginized eczema 33 24.09 Lichenified eczema 45 32.85 Eczema vulgar 66 48.18 Table 3: Various complications observed Complications (C) (n=137) Number Percentage Growth retardation 0 0.00 Ophthalmology 0 0.00 Psychic impact 1 0.73 Contact dermatitis 2 1.46 Impetiginization 33 24.09 Lichenification 45 32.85 Figure 2: Lichenified and impetiginized eczema
  • 4. Agbessi: Atopic dermatitis in children in Parakou (Benin) 9 Clinical Research in Dermatology  •  Vol 3  •  Issue 1  •  2020 of Benin (in Cotonou in 2009) in the hospital population, this one had the merit of taking stock of the situation of AD in the general pediatric population. A better knowledge of the manifestations of AD would help physicians in general and pediatricians in particular to better manage it. The majority of these children do not come to the dermatologist’s office as a first-line treatment; especially in our sub-Saharan African countries where access to specialized care is still a luxury for the most vulnerable populations. REFERENCES 1. Dammak A, Guillet G. Atopic dermatitis in children. J Pediatr Child Care 2011;24:84-102. 2. Catteau B. Atopic dermatitis: Epidemiology and current clinical data. Rev Fr Allergol Immunol Clin 2002;42:373-7. 3. Kobangué L, Piamalé G, Bureau JJ, Sépou A. Epidemiological and clinical aspects of atopic dermatitis at the National Hospital and University Centre of Bangui. Ann Dermatol Venereol 2007;134 Suppl 1:S98. 4. Atadokpédé F, Adégbidi H, Koudoukpo C, Agbessi N, Yedomon H, do-Ango-Padonou F, et al. Atopic dermatitis in Cotonou, Benin: Clinical and therapeutic aspects. Dakar Med 2012;57:1-7. 5. Nnoruka EN. Current epidemiology of atopic dermatitis in South-Eastern Nigeria. Int J Dermatol 2004 43:739-44. 6. Yu SH, Attarian H, Zee P, Silverberg JI. Burden of sleep and fatigue in US adults with atopic dermatitis. Dermatitis 2016;27:50-8. 7. Koudoukpo C, Akpadjan F, Agbessi N, Dégboé B, Nouhoumon G, Adégbidi H, et al. Epidemiological aspects of atopic dermatitis in Borgou-Alibori Teaching Hospital of Parakou (Benin). Health Sci Dis 2019;20:94-7. 8. BainoA, Hocar O,Akhdari N,Amal S. Prevalence and clinical- epidemiological profile of dermatitis atopic in Morocco. Ann Dermatol Venereol 2016;143 Suppl 1:S43-4. 9. Djénabou A. Atopic eczema in adolescents in Yaoundé, Cameroon. Rev Fr Allergol 2017;57:265-83. 10. Técléssou JN, Mouhari-Toure A, Akakpo S, Bayaki S, Boukari OB, Gnassingbe W, et al. Risk factors and allergic manifestations associated with atopic dermatitis in Lomé (Togo): A multicenter study of 476 children aged 0-15 years. Méd Santé Trop 2016;26:88-91. 11. Baghou S, Bensaad D, Taieb A, Ammar-Khodja A. Prevalence and clinical profile of atopic dermatitis in Algeria. Ann Dermatol Venereol 2012;139:140. 12. Hagendorens MM, Bridts CH, Lauwers K. Perinatal risk factors for sensitization, atopic dermatitis and wheezing during the first year of life (PIPO study). Clin Exp Allergy 2005;35:733-40. How to cite this article: Agbessi N, Akpadjan F, Dégboé B, Nouhoumon G, Koudoukpo C, Adegbidi H, Atadokpédé F. Epidemio-clinical Profile of Atopic Dermatitis in Children in General Population in Parakou (Benin). Clinic Res Dermatol 2020;3(1):6-9.