|Year : 2022 | Volume
| Issue : 1 | Page : 30-34
Prevalence and risk factors of vulvar dermatoses: A hospital-based study
Ashwini Dattatray Mundhe1, Avinash Jadhav1, Kirti Deo1, Mahendra Singh Deora1, Rohini Gaikwad2, Rajendra C Shinde3
1 Department of Dermatology, Dr. D. Y. Patil Medical College and Hospital, Pune, Maharashtra, India
2 Aashay the Skin Clinic, Pune, Maharashtra, India
3 Department of Dermatology, MIMER Medical College and hospital, Pune, Maharashtra, India
|Date of Submission||08-Dec-2021|
|Date of Decision||16-Mar-2022|
|Date of Acceptance||08-Apr-2022|
|Date of Web Publication||07-Jun-2022|
Dr. Avinash Jadhav
Param, 129/1, Plot No. 7, Baner Balewadi Road, Baner, Pune - 411 045, Maharashtra
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: The overall prevalence of vulvar diseases in the literature is low because of underreporting and is often neglected; thus, its impact on a female's life is often underestimated. Objectives: This study is aimed to determine the prevalence of vulvar diseases and their associated risk factors in patients attending a tertiary care hospital. Materials and Methods: This is a descriptive, cross-sectional, and case–controlled study wherein all female patients attending the dermatology outpatient department (OPD) were screened for the signs and symptoms of vulvar dermatoses and were enrolled after obtaining informed consent and institutional ethics committee approval for 21 months. Out of them, 200 patients who consented and had signs and symptoms of vulvar diseases were selected as cases, and the same number of age-matched females were enrolled as controls with no signs and symptoms of vulvar dermatoses. Results: During the study period, 9431 females attended the dermatology OPD, of which the prevalence was 2.12% (200 patients). The most common infection was genital infection without sexually transmitted infection (57%) (tinea cruris [33.5%]), followed by inflammatory dermatoses (21%) (lichen sclerosus et atrophicus [6%]). The most common risk factor found statistically significant (P ≤ 0.005) were homemakers (49%) and the use of undergarments of mixed fabric (70.68%), followed by nonmenopausal females (63.15%). Conclusion: Our study findings indicated that the prevalence was low, which reflects the tip of an iceberg. Further clinical and population-based studies, a multidisciplinary approach including gynecological consult for diagnostic and therapeutic approach is needed for the optimal management of vulvar diseases.
Keywords: Prevalence, risk factors, vulvar diseases
|How to cite this article:|
Mundhe AD, Jadhav A, Deo K, Deora MS, Gaikwad R, Shinde RC. Prevalence and risk factors of vulvar dermatoses: A hospital-based study. Indian J Sex Transm Dis 2022;43:30-4
|How to cite this URL:|
Mundhe AD, Jadhav A, Deo K, Deora MS, Gaikwad R, Shinde RC. Prevalence and risk factors of vulvar dermatoses: A hospital-based study. Indian J Sex Transm Dis [serial online] 2022 [cited 2022 Nov 28];43:30-4. Available from: https://www.ijstd.org/text.asp?2022/43/1/30/346597
| Introduction|| |
The vulva has been referred to as “the forgotten pelvic organ.” Vulvar dermatoses are skin disorders that affect the vulva. They may be asymptomatic or may present with itching, burning, dyspareunia, pain, fissuring, sometimes bleeding after intercourse, and discomfort. Its anatomical and physiological characteristics create additional diagnostic and therapeutic difficulties. The study of vulvar diseases is emerging as a new branch of dermatology. Many women are not examined and are misdiagnosed with “thrush.” Self-treatment with topical medications (steroid abuse) may delay accurate diagnosis and increase the risk of secondary irritant reactions. When the problem is thought to be in the anogenital skin, referral to a dermatologist or a vulvar clinic is appropriate.
The skin disorders of the genitalia can be grouped into the following categories: (1) normal anatomical variants, (2) sexually transmitted infections (STIs) affect the genitals, (3) genital infections other than sexually transmitted diseases (STDs), (4) bullous dermatoses, (5) inflammatory conditions, (6) premalignant dermatoses, (7) malignant diseases of genitalia, and (8) others.
The incidence and prevalence of dermatoses affecting female genitalia and their etiopathogenesis are generally not well established. The prevalence is high in developing countries as compared to developed countries. Disease courses affecting other areas of the body are better characterized, but the environment of the vulva strongly affects the course of the disease.
The purpose of the study was to investigate the magnitude of the frequency of vulvar diseases, their clinical patterns, and the risk factors associated with the enrolled patients.
Aims and objectives
This study aimed to study the prevalence of vulvar dermatoses, the different clinical patterns, and its associated risk factors.
| Materials and Methods|| |
The present study was carried out at the dermatology outpatient department (OPD) in tertiary care hospital after obtaining Institutional Ethical Clearance. It is a descriptive, cross-sectional, and case–controlled study carried out for 21 months. Cases and age-matched controls visiting the OPD were enrolled during the study duration. All newly registered female patients were screened for vulvar dermatoses, out of which 200 patients with vulvar dermatoses were taken as cases after counseling, who have not taken any prior treatment and obtaining informed written consent. Patients with vulvar dermatoses taking treatment before the visit and patients not consenting were excluded from the study. An equal number of age-matched females without vulvar lesions or symptoms were selected as controls. Detailed clinical examination, laboratory investigations such as complete blood count, blood sugar level, urine routine and microscopy, Gram staining, and KOH mount of the patients were done according to the case study proforma. The risk factors such as marital status, occupation, use of undergarments and detergent, menopause, and menstrual history were ruled out, investigated, and treated wherever needed.
Data analysis was performed using the SPSS (Statistical Package for the Social Sciences) software version 17 of Windows. Data were expressed in descriptive statistics. The duration and diagnosis of the disease were calculated with number and percentage. The t-test was applied to find whether the difference of age between cases and controls was significant. The Chi-square test was applied to find the association of age, marital status, occupation, type of detergent, type of undergarments, menopause, and menstrual history between both groups. P ≤ 0.05 was accepted as the level statistically significant.
| Results|| |
The prevalence of vulvar dermatoses (200 cases) is 2.12% [Figure 1]. The mean age of cases is 30.94 standard deviation ± 14.29 years which is not significant (P > 0.05) [Table 1]. Married women, homemakers, use of mixed types of undergarments, and menopausal women were significantly at risk, but not significant with the use of detergent and menstrual history [Table 2]. Tinea cruris (67, 33.5%) is seen most frequently, followed by candidal vulvovaginitis (34, 17%) [Table 3]. There is a statistically significant (P < 0.05) association between vulvar dermatoses and age with the largely affected group of 16 and 30 years with genital infections other than STD (67 cases), followed by STDs (20 cases) [Table 4].
|Figure 1: (a) Lichen sclerosus et atrophicus (b) Herpes genitalis (c) Condyloma accuminata (d) Vitligo|
Click here to view
| Discussion|| |
Although there are several reports on the study of individual vulvar disorders in the literature, there is a paucity of studies that have systematically studied the prevalence, associations, and risk factors of vulvar dermatoses altogether. This study consists of a series of 200 cases of vulvar dermatoses out of 9431 female patients attending the OPD of a tertiary care center during the study period of 21 months.
The prevalence of vulvar diseases accounted for 2.12% of all dermatological disorders recorded among all the female patients [Figure 1]. It is comparable and similar to the findings of Pathak et al. reported 1.9%.
The mean age of the patients was 30.94 ± 14.29 years [Table 1] which is similar to the study by Gokdemir et al.
There is a significant association of vulvar dermatoses with age wherein the maximum number of patients were from the age group of 16–30 years (42.5%), followed by 31–45 years (25.5%) which is similar to the study by Pathak et al. This could be attributed to more sexual activity in these groups. The duration of lesions reported in maximum cases was <1 month (69%).
On analysis of the demographic data of the patients including marital status and occupation, the majority of the patients were married (69%), among which maximum cases were homemakers (49%), followed by students (28.5%) [Table 2]. This is comparable to the study by Pathak et al.
The majority of patients used detergent in the form of powder (52.5%) to wash the undergarments, which does not seem to contribute to vulvar dermatoses in our study [Table 2]. However, Pathak et al. have shown a significant association with the use of powder for washing undergarments. Washing of undergarments with hypoallergenic soaps is recommended as anything that is irritant can lead to itching, soreness of the skin, and irritation.
Mixed-type fabric undergarments (70.68%) are commonly used, followed by cotton fabric (48.09%) which was significantly associated in both cases and controls [Table 2] which contrasts with the study by Pathak et al. where nylon undergarments were a major contributing factor for vulvar dermatoses. The use of the mixed or polyester type of undergarments causes sweat, moisture, and humidity retention by trapping moisture and air between the skin and the fabric, creating a favorable environment for organisms such as bacteria and fungi to thrive which may result in urinary tract infection, bacterial, and fungal skin infections. Furthermore, tight undergarments can potentially cause slow blood circulation.
The correlation between menopause and vulvar dermatoses has not been explored. In this study, a statistically significant difference was observed between menopausal and nonmenopausal females [Table 2]. Menstruating females were found to have a significantly higher incidence due to improper hygiene practices, use of sanitary napkins for a long duration, and sexual activity. Menstrual irregularity was not found to be a significant contributing factor in causing vulvar dermatoses in our study which contrasts with the study by Pathak et al., where it was found significant. Family history was found to be contributory in our study. This could be due to poor hygiene, overcrowding, and sharing of towels and clothes among each other.
The most common causes of vulvar dermatoses were genital infections other than STD (57%) [Table 3] found in our study. These findings were similar to studies by Pathak et al. and Bauer et al., where fungal and bacterial infections were observed frequently.,
The most common infection in our study was tinea cruris (33.5%), followed by candidal vulvovaginitis (17%) which contrasts with the study by Buscemi et al. and Patel et al. where candidal vulvovaginitis (11.4%) was more prevalent. However, in the study by Sullivan et al., lichen sclerosus et atrophicus (LSetA) (26%) was the most common, followed by candidal vulvovaginitis (16%), while Puri et al. reported 31% of candidal vulvovaginitis.,,,
The second most common condition observed was bacterial infections wherein superficial folliculitis (4.5%) followed by deep folliculitis (1.5%) was seen in this study which was almost similar to the study by Pathak et al. (5.7%).
Among viral infections, varicella was seen in 0.5%, in contrast to Pathak et al., who reported 1.9% of the same.
STDs were reported in 27 (13.5%) cases, among which herpes genitalis (10, 5%) was found to be commonly, followed by molluscum contagiosum (84%), condyloma acuminata (5, 2.5%), chancroid (3, 1.5%), and phthiriasis pubis (1, 0.5%) among the cases in our study. Whereas in the study by Pathak et al., condyloma acuminata (7.6%) was seen commonly, followed by herpes genitalis (0.9%). Koutsky et al. reported 1% of sexually active females (age 15–49) with condyloma acuminata and 1.5% was reported by Fischer and Rogers., Molluscum contagiosum was reported by Fischer and Rogers in 0.7%, Singh et al. in 0.8% cases, and Priya et al. reported 5.7%.,, Phthiriasis pubis was reported by Bignell in 2% and Hart reported 1.1% in their studies.,
Among the inflammatory conditions, LSetA (6%) was more prevalent, followed by lichen simplex chronicus (LSC) (2.5%) which is almost similar to the study by Pathak et al. where LSetA (2.9%) and LSC (0.9%) were reported. This was in contrast with a study by Sullivan et al. wherein they reported LSetA in 26% of cases, Fischer and Rogers reported 17%, and Cheung et al. reported 21%.,,
Atrophic vulvovaginitis was observed in 2.5% of cases belonging to age groups 16–30 and 31–45 years compared to 1.9% in a previous study by Pathak et al., whereas it was observed in 40% of cases by Tobin and Harindra who has carried out the study in female aged 50 years and above.,
Vulvar psoriasis is a very rare inflammatory condition, and in this study, it was seen in four cases (2%) not exclusively on the vulva as other cutaneous areas were also involved. The study by Pathak et al. showed 1.9%, whereas similar results were reported by Fischer and Rogers showed 12%, Hammock and Barrett which showed 2%, Heller et al. showed 1.8%, and Fischer and Rogers showed 5%.,,,,
Exclusive vulvar lichen planus was seen in 3% of cases without dermatological involvement. Lewis et al. reported 51% of cases as a part of generalized lichen planus.
In this study, vitiligo was seen in 1.5%, whereas Pathak et al. reported 5.7% and Fischer and Rogers reported 0.7% cases.,
In this study, irritant contact dermatitis (ICD) was reported in 0.5% of cases, whereas a study by Singh et al. reported 1.6% of cases. Agents usually responsible for irritant dermatitis include cleansing agents, depilatory creams, disinfectants, sanitary napkins, latex condoms, perfumed products, deodorants, and medicaments. It usually occurs because of an impairment of the barrier function which may occur due to dampness and maceration secondary to a heavy vaginal discharge or increased contact with urine in an incontinent patient., ICD occurs more frequently than allergic contact dermatitis.
Among the bullous disorders pemphigus vulgaris and fixed drug eruptions, 1% each were seen in our study but not exclusively on the vulva as other cutaneous areas were also involved which is almost similar to the findings of Pathak et al. (0.9%). Furthermore, erythema multiforme was reported in 0.5% of cases.
Vulvar acrochordons were seen in 2% of cases, whereas Singh et al. reported in 1.6% and Priya et al. reported 2.8% cases and Puri and Puri reported in 5% of cases.,,
Finally, pruritus vulvae are a common symptom with a multifactorial origin which often significantly impairs the patient's quality of life, impacting sexual function, relationships, sleep, and self-esteem. In our study, pruritus vulvae not associated with any particular dermatoses were observed in 6.5% of the cases, which was in contrast to the previous study by Pathak et al. who reported 36.2% of the cases where psychological, social, behavioral, and sexual factors were seen to influence the prevalence of the condition. Other studies by Gokdemir et al. reported 26.5% of cases and Paek et al. reported 75%.,
Thus, this study indicates that infectious conditions predominate over inflammatory ones in developing countries such as India while the opposite is observed in developed countries. Hence also, age is an important determinant in the occurrence of various conditions. Younger females are more affected by infections and menopausal women present with inflammatory conditions. This can be mitigated by imparting sex education and good hygienical practices to high school girls. While we did not encounter any malignant conditions, but frequent screening of menopausal women should be undertaken because long-standing inflammatory conditions can predispose them to malignancy.
However, since pregnant females, females taking prior treatment and use of over-the-counter drugs, and those who have not consented were excluded large population-based studies are required to estimate the exact impact on the female population.
| Conclusion|| |
The prevalence of vulvar dermatoses in this study was 2.12% which only reflects the tip of an iceberg of the actual patients who suffer from similar problems. The most common vulvar dermatoses in this study were of infections in which the dermatophytosis was the most frequent to occur with the predominance of tinea cruris. Although the married population, homemakers, use of mixed fabric undergarments, menopause, and family history were found to be significant with an increased incidence of vulvar dermatoses, in reality, it is difficult to establish in such a small study.
Multidisciplinary specialty clinics including gynecological consultation should be made available for a diagnostic and therapeutic approach that will cover all the vulvar dermatoses. Increasing awareness among the female population and encouraging them to seek treatment for the diseases and avoid self-medication is of paramount importance.
Our study findings indicate that the known frequency of vulvar dermatoses represents only a small proportion of the actual affected population. Further clinical and large population-based research study is a need concerning the treatment, follow-up, and true prevalence of these diseases in the community.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Noller KL. Vulva: The forgotten pelvic organ. Obstet Gynecol 2004;104:913-4.
Thomas J. Genital dermatoses. In: Parimalam K, Sindhu RB, Dinesh KD, editors. Genital Dermatoses. 1st
ed. Jaypee Brothers Medical Publishers New Delhi; 2016. p. 6-215.
Pathak D, Agrawal S, Dhali TK. Prevalences of and risk factors for vulvar diseases in Nepal: A hospital-based study. Int J Dermatol 2011;50:161-7.
Gokdemir G, Baksu B, Baksu A, Davas I, Koslu A. Features of patients with vulvar dermatoses in dermatologic and gynecologic practice in Turkey: Is there a need for an interdisciplinary approach? J Obstet Gynaecol Res 2005;31:427-31.
Bauer A, Greif C, Vollandt R, Merker A, Elsner P. Vulval diseases need an interdisciplinary approach. Dermatology 1999;199:223-6.
Buscemi L, Arechavala A, Negroni R. Study of acute vulvovaginitis in sexually active adult women, with special reference to candidosis, in patients of the Francisco J. Muñiz Infectious Diseases Hospital. Rev Iberoam Micol 2004;21:177-81.
Patel V, Weiss HA, Mabey D, West B, D'Souza S, Patil V, et al
. The burden and determinants of reproductive tract infections in India: A population based study of women in Goa, India. Sex Transm Infect 2006;82:243-9.
Sullivan AK, Straughair GJ, Marwood RP, Staughton RC, Barton SE. A multidisciplinary vulva clinic: The role of genito-urinary medicine. J Eur Acad Dermatol Venereol 1999;13:36-40.
Puri KJ, Madan A, Bajaj K. Incidence of various causes of vaginal discharge among sexually active females in age group 20-40 years. Indian J Dermatol Venereol Leprol 2003;69:122-5.
] [Full text]
Koutsky LA, Galloway DA, Holmes KK. Epidemiology of genital human papillomavirus infection. Epidemiol Rev 1988;10:122-63.
Fischer G, Rogers M. Vulvar disease in children: A clinical audit of 130 cases. Pediatr Dermatol 2000;17:1-6.
Singh N, Thappa DM, Jaisankar TJ, Habeebullah S. Pattern of non-venereal dermatoses of female external genitalia in South India. Dermatol Online J 2008;14:1.
Priya BT, Muthupandian V, Alagar K, Kannan R. A retrospective study on the incidence of non-venereal genital dermatoses in patients attending STI clinic at a tertiary care center. Int J Res Dermatol 2017;3:254-60.
Bignell C. Lice and scabies. Medicine 2005;33:76-7.
Hart G. Factors associated with pediculosis pubis and scabies. Sex Transm Infect 1992;68:294-5.
Cheung ST, Gach JE, Lewis FM. A retrospective study of the referral patterns to a vulval clinic: Highlighting educational needs in this subspecialty. J Obstet Gynaecol 2006;26:435-7.
Tobin J, Harindra V. Atrophic vulvovaginitis in women aged 50 years and above, both current and non-users of hormone replacement therapy, attending a genitourinary medicine clinic. J Fam Plann Reprod Health Care 2002;28:135-6.
Hammock LA, Barrett TL. Inflammatory dermatoses of the vulva. J Cutan Pathol 2005;32:604-11.
Heller DS, Randolph P, Young A, Tancer ML, Fromer D. The cutaneous-vulvar clinic revisited: A 5-year experience of the Columbia Presbyterian Medical Center Cutaneous-Vulvar Service. Dermatology 1997;195:26-9.
Fischer GO. The commonest causes of symptomatic vulvar disease: A dermatologist's perspective. Australas J Dermatol 1996;37:12-8.
Lewis FM, Shah M, Harrington CI. Vulval involvement in lichen planus: A study of 37 women. Br J Dermatol 1996;135:89-91.
Garg T, Mittal S. Vesicobullous disorders of female genitalia. Indian J Sex Transm Dis AIDS 2012;33:1-8.
Britz MB, Maibach HI. Human cutaneous vulvar reactivity to irritants. Contact Dermatitis 1979;5:375-7.
Elsner P, Wilhelm D, Maibach HI. Multiple parameter assessment of vulvar irritant contact dermatitis. Contact Dermatitis 1990;23:20-6.
Schlosser BJ. Contact dermatitis of the vulva. Dermatol Clin 2010;28:697-706.
Puri N, Puri A. A study on non-venereal genital dermatoses in north India. Our Dermatol Online 2012;3:304-7.
Paek SC, Merritt DF, Mallory SB. Pruritus vulvae in prepubertal children. J Am Acad Dermatol 2001;44:795-802.
[Table 1], [Table 2], [Table 3], [Table 4]