ARTICLE
Auteur(s) : Elvir Cesko, Andreas Körber, Joachim Dissemond
Department of Dermatology, Venerology and Allergology,
University of Essen, Hufelandstr. 55, 45177 Essen, Germany
accepté le 1 Avril 2009
Acne inversa is a chronic, recurring, suppurative, acneiform
skin disease with inflammation of the follicular epithelium of the
sebaceous glands and the terminal hair follicle. It primarily
manifests in the intertriginous areas. Eccrine and apocrine sweat
glands are drawn into the inflammation process secondarily [1]. The
disease pattern was described first in 1839 by the French
physician, Velpeu, as a specific inflammatory process with
superficial abscess formation in the axilla, chest and perianal
areas. Due to the distribution, it was originally viewed as a
disease of the sweat glands. In 1956, Pillsbury and co-workers
coined the term “follicular occlusion triad” to describe the triad
of acne conglobata, hidradenitis suppurativa and perifolliculitis
capitis abscedens et suffodiens. In 1975, Plewig and Steger
incorporated a final symptom, the pilonidal sinus, to the clinical
picture of acne triad and changed the nomenclature to “acne tetrad”
[1]. After the follicular origin of the disease was confirmed in
further studies, Plewig and Steger introduced the term “acne
inversa” in 1989. Currently, this term has almost completely
replaced the term “hidradenitis suppurativa”, at least in the
German speaking countries [2].
An incidence of 0.3% to 4% in industrialized countries is
described for acne inversa [3]. The ratio of women to men is
reported to be 2-5:1 [1]. Men often develop acne inversa in the
perianal area and present a more severe degree than women, who are
often affected in the axilla [4]. The initial manifestation can be
observed from the age of 12 and is not age-restricted. Usually, the
disease manifests predominantly in young adults. Up to now, the
exact aetiology of acne inversa is unknown [5]. The association
with nicotine consumption has been discussed repeatedly [5, 6].
Scientific data concerning the negative effects of smoking exist,
especially for cardiovascular diseases and neoplasms. Although a
negative influence on psoriasis vulgaris, wound healing or skin
ageing have been described empirically, hardly any scientific
studies exist that confirm the development or exacerbation of
dermatological diseases through nicotine consumption. Therefore,
the aim of our study was to investigate influencing factors in a
group of 100 patients with acne inversa.
Methods and patients
Patients
In this study the files of 100 acne inversa patients, who were
treated on an inpatient basis in the University Clinic for
Dermatology, Venerology and Allergology, Essen, Germany in
2002-2006 were analysed retrospectively. All diagnoses were
confirmed by a histopathological analysis of a biopsy.
Collected parameters
The following parameters were analysed for as many patients as
possible: age, BMI, sex, weight, height, ethnic origin,
localisation of acne inversa, smoking quantity, smoking behaviour
(active smoker, former smoker, non-smoker), date of initial acne
inversa diagnosis.
The Body Mass Index (BMI) was determined as follows: The ratio
between the weight and height squared.
Statistical analysis
The programme Microsoft® Excel 2000 was used for the
statistical analysis. A value of p < 0.05 was assessed.
Results
Sex ratio
The examined patient group consisted of 51 women and 49 men. In so
far, no significantly higher proportion of women with acne inversa
could be determined.
Age
The average age of the patients examined was 37.8 years. When
differentiating between the sexes, the women had a lower average
age of 35.5 years, compared to the men of 40.1 years.
Localisation of acne inversa
In the case of 23 patients, the acne inversa was exclusively
axillary, 22 patients axillary and inguinal, 19 patients inguinal,
15 patients axillary, inguinal and genital, 7 patients gluteal and
genital and 2 patients nuchal. In the case of 5 patients, the
localisation could not be exactly specified. When considering the
sexes separately, the following scenario was shown. In the
51 female patients, the acne inversa was exclusively axillary
in 9 patients, axillary and inguinal in 11 cases,
inguinal in 13 cases, axillary, inguinal and genital in 11
cases, gluteal in 3 cases, nuchal in 1 case and not analyzable in 3
cases. In the 49 male patients, the acne inversa was
exclusively axillary in 14 patients, axillary and inguinal in 11
patients, genital in 7 cases, inguinal in 6 cases, both
axillary, inguinal and genital and also exclusively gluteal in
4 cases, nuchal in 1 case, and not evaluable in
2 cases (table 1).
Table 1 Localisation of the acne inversa
|
Localisation
|
Numbers
|
|
Men
|
Women
|
Total
|
|
Axillary
|
14
|
9
|
23
|
|
Axillary + inguinal
|
11
|
11
|
22
|
|
Inguinal
|
6
|
13
|
19
|
|
Axillary + inguinal + genital
|
4
|
11
|
15
|
|
Gluteal
|
4
|
3
|
7
|
|
Genital
|
7
|
0
|
7
|
|
Nuchal
|
1
|
1
|
2
|
|
No data
|
2
|
3
|
5
|
|
Total
|
49
|
51
|
100
|
Smoking behaviour
All in all, 87 patients indicated that they were currently active
smokers and 11 patients stated that they were former smokers. Thus,
98 (50 female, 48 male) of the 100 patients either smoke currently
or smoked regularly in the past. All smokers, included former
smokers, indicated that they smoked cigarettes primarily or
exclusively. Only 2 patients had a negative smoking history.
Smoking quantity and duration
With reference to the quantity of smoking, details of 81 patients
were available. These patients smoked an average of 22.5 cigarettes
a day. When differentiating between the sexes, the following
picture was revealed. The 41 women, for whom details of the
quantity of smoking were available, smoked an average of 20.8
cigarettes a day. The 40 male patients smoked an average of 24.1
cigarettes a day.
In 28 cases, details of the duration of nicotine consumption
were available. The average value was 19.1 years (2-40 years).
When differentiating between the sexes, the female patients
presented a lower value of 16.3 years (2-30 years), compared
to the 13 male patients, with a value of 22.4 years (10-40 years)
with regard to the duration of nicotine consumption.
Latent phase from the initiation of smoking
to the initial acne inversa diagnosis
In 18 cases complete particulars, with regards to the latent phase
from the initiation of smoking to the presentation of the first
acne inversa symptoms, were presented. Thus, the initial
presentation of acne inversa appeared after an average of 12.8
years (1-35 years) after the start of cigarette smoking. When
differentiating between the sexes, men showed a longer average
latent phase (n = 10) than women. Their latent phase is an average
of 15.6 years until the onset of acne inversa, whereas the women
showed an average of 9.3 years (n = 8). In 2 cases the diagnosis of
acne inversa was already manifest for a few years before the
beginning of cigarette smoking. In the case of the male patient,
the diagnosis was already manifest for 15 years and in the case of
the female patient for 8 years, so that cigarette smoking could not
have played a role in the presentation of the first acne inversa
symptoms.
Weight
The average patient weight was 88.5 kg (n = 88). When
differentiating between the sexes, the women showed a lower average
weight of 79.5 kg (n = 43), compared to the men, with an
average weight of 97.1 kg (n = 45).
BMI (Body-Mass-Index)
The average body mass index (BMI) of the examined patients was 28.6
(n = 88). When differentiating between the sexes, the women showed
a lower BMI of 27.8, compared to the men with 29.3 (table 2). Hence, a total of 51.1% of the patients
fell into the category overweight. Only 26.1% of the patients had a
normal weight. One female patient was underweight (table 3).
Table 2 Weight classification of the adults on the
basis of BMI according to WHO
|
Category
|
BMI
|
Risk of secondary disorders
|
|
Underweight
|
< 18.5
|
Low
|
|
Normal weight
|
18.5-24.9
|
Average
|
|
Overweight
|
≥ 25
|
|
|
Pre-obesity
|
25-29.9
|
Slightly raised
|
|
Obesity grade I
|
30-34.9
|
Raised
|
|
Obesity grade II
|
35-39.9
|
High
|
|
Obesity grade III
|
≥ 40
|
Very high
|
Table 3 Weight classification of the examined patients
on the basis of BMI (n = 88)
|
Category
|
Total
|
Male
|
Female
|
German population Male (2005)
|
German population Female (2005)
|
|
Underweight
|
1 (1.1%)
|
0
|
1
|
1%
|
4%
|
|
Normal weight
|
23 (26.1%)
|
11
|
12
|
|
|
|
Overweight
|
|
|
|
|
|
|
Pre-obesity
|
19 (21.6%)
|
10
|
9
|
|
|
|
Obesity grade I
|
32 (36.4%)
|
18
|
14
|
14%
|
13%
|
|
Obesity grade II
|
8 (9.1%)
|
3
|
5
|
|
|
|
Obesity grade III
|
5 (5.7%)
|
3
|
2
|
|
|
|
64 (72.7%)
|
34
|
30
|
|
|
|
Total
|
88 (100%)
|
45 (51.1%)
|
43 (48.9%)
|
|
|
Discussion
Already in 1989, Plewig and Steger described acne inversa
histopathomorphologically as a disease pattern which primarily
affects the hair follicles. It could be proven that a
hyperkeratosis of the folliclar infundibulum results in comedo
formation with subsequent superinfection and segmental rupture of
the follicular epithelium [2]. A granulomatic inflammation of
the connective tissue, with formation of cutaneous and subcutaneous
lumps, develops as a reaction to the foreign matter released. After
the rupture of the follicular epithelium, the disease advances
rapidly with development of abscesses, fistulas and consecutive
fibrosis. Eccrine and apocrine sweat glands are involved in a
secondary inflammation [1]. To date it is not clear which factors
lead to follicular occlusion. Neither obesity, nor other factors
discussed, such as chemical irritants, depilation, mechanical
irritants or shaving could be confirmed so far in bigger clinical
studies [7, 8]. Bacterial colonisation could also not be confirmed
up to now as a primary pathogenetically relevant factor. In fact,
the bacterial superinfection should rather be viewed as secondary
to the actual disease pattern.
Nicotine consumption has a negative influence on many skin
diseases [9]. Nicotine, with its damaging capacity, mainly attacks
the blood and vascular systems, the collagen metabolism and the
interactions on an immunological basis. In the context of wound
healing, and respectively, wound healing disturbances, for example,
altered rheological characteristics of the blood, an increased
vasoconstriction and vessel wall epithelium damages present
important factors in the development of the disease and its
progression [9]. The empirically described high incidence of
smokers amongst acne inversa patients suggests that nicotine
consumption could be a trigger for acne inversa [10]. The
combination of a reduced circulation of the inflamed tissue with a
reduced humoral and cellular immune reaction seems to be a relevant
precondition for the chronicity of the disease pattern [11]. In
vitro studies on the influence of nicotine on neutrophile
granulocytes have shown that the suppression of apoptosis by
nicotine leads to a prolonged survival of the neutrophile
granulocytes. Furthermore, their reactivity to chemotactic peptides
is increased, so that tissue inflammation is promoted [1].
In a study published in 1999, it was shown that 89.9% of 63 acne
inversa patients were smokers. In the control group chosen, there
were only 46% smokers [5]. In a study published in 1995 by
Breitkopf et al., similar results were shown, with 85% of 149
examined acne inversa patients being smokers. The results of our
study show similar results, although our smoker quota of 98% was
noticeably higher. In two cases the diagnosis of acne inversa was
already manifest a few years before the beginning of cigarette
smoking. So the proportion of smokers which is relevant for the
first manifestation of acne inversa is 96% (table 4). According to statistics of the Federal
Statistical Office of Germany from 2006, 73% of the adult
population in Germany is comprised of non-smokers. However, 19% of
these were former smokers [12]. The data collected in the context
of this study confirms the results published so far and shows that
the proportion of smokers amongst acne inversa patients is
significantly higher compared to the number of smokers in the
general population.
Obesity is defined as an increase in body fat exceeding normal
limits. The most common basis for calculation of the weight class
is the Body Mass Index (BMI). According to the WHO, overweight is
defined as BMI ≥ 25 kg/m2, obese as BMI ≥ 30
kg/m2 (table 2). The
prevalence of obesity (BMI ≥ 30 kg/m2) has been
continuously increasing in recent decades in Germany. In 1998
18.3-24.5% of the German population in the age group 18-79 years
showed a BMI of > 30. Added to this, 31.1-48.7% of the
population was already overweight with a BMI of between 25.0 and
29.9 [13]. Obesity is also often under discussion as an etiological
factor concerning the development of acne inversa [10]. In a study
carried out by Jemec, the weight of acne inversa patients was
compared to the corresponding ideal weight. No significant
differences were found [8]. In a study done by Werth and Williams,
45% of the 110 interviewed patients reported a worsening of the
disease due to heat and sweating, 16% reported a worsening caused
by tight-fitting clothing and friction and a third indicated a
worsening during the summer months [14]. In the group we examined,
more than a half had a BMI of > 30. 72.7% fall at least into the
category pre-obesity (table 3). Only
26.1% of the patients showed a normal weight (table 3). These results deviate significantly from
the average values of the adult German population and could
therefore be discussed as a further aetiologically potentially
relevant factor concerning acne inversa. Yet, it could also be
possible that the obesity could be secondarily promoted by the
inactivity that so often results from the acne inversa.
Table 4 Quota of smokers among acne inversa patients
(comparison of different studies)
|
Studies
|
Acne inversa patients
|
Quota of smokers
|
|
König et al. 1999
|
63
|
89.9%
|
|
Breitkopf et al. 1995
|
149
|
85%
|
|
Cesko et al. 2009
|
100
|
96%
|
Conclusion
The results of our retrospective study demonstrate that the
proportion of smokers and persons with obesity, in comparison with
the normal adult population, is significantly higher in 100 acne
inversa patients. These data, which were collected in a large group
of acne inversa patients, confirm the necessity of considering the
associated and potentially aetiopathologically relevant factors for
a long term, successful treatment of patients with acne inversa.
Acknowledgements
Conflict of interest: none. Financial support: none.
References
1 Stein A, Sebastian G. Acne inversa. Hautarzt 2003; 54:
173-87.
2 Plewig G, Steger M. Acne invesa. In: Marks R,
Plewig G, eds. Acne and related disorders. London: Martin
Dunitz, 1989: 345-57.
3 Brown TJ, Rosen T, Orengo IF. Hiddradenitis
suppurativa. South Med J 1998; 91: 1107-14.
4 Jemec GBE. The symptomatology of hidradenitis suppurativa
in women. Br J Dermatol 1988; 119: 345-50.
5 König A, Lehmann C, Rompel R, Happle R.
Cigarette smoking as a triggering factor of hidradenitis
suppuativa. Dermatology 1999; 198: 261-4.
6 Yu CC, Cook MG. Hidradenitis suppurativa: a disease
of follicular epithelium, rather than apocrine glands. Br J Dermato
1990; 122: 763-9.
7 Morgan WP, Leicester G. The role of depilation and
deodorants in hidradenitis suppurativa. Arch Dermatol 1982; 118:
101-2.
8 Jemec GBE. Body weight in hidradenitis suppurativa. In:
Marks R, Plewig G, eds. Acne and related disorders.
London: Martin Dunitz, 1989: 365-6.
9 Krug M, Wünsche A, Blum A. Tabakabhängigkeit
und die Folgen auf die Haut. Hautarzt 2004; 55: 301-16.
10 Jansen T, Altmeyer P, Plewig G. Acne inversa
(alias hidradenitis suppurativa). J Eur Acad Dermatol Venereol
2001; 15: 532-40.
11 Smith JB, Fenske NA. Cutaneous manifestations and
consequences of smoking. J Am Acad Dermatol 1996; 34: 717-32.
12 Statistisches Bundesamt Deutschland: Drei Viertel der
Bevölkerung in Deutschland sind Nichtraucher. Online Communication
2006; No. 249.
13 Bergmann KE, Mensink GB. Körpermaße und
Übergewicht. Gesundheitswesen 1999; 61: 115-20.
14 von der Werth JM, Williams HC. The natural history
of hidradenitis suppurativa. J Eur Acad Dermatol Venereol 2000; 14:
389-92.
|