Common Benign Chronic Vulvar Disorders

Nancy E. Ringel, MD
Cheryl Iglesia, MD

American Family Physician. 2020;102(9):550-557.

Author disclosure: No relevant financial affiliations.

Patient information: See related handout on genitourinary syndrome of menopause, written by the authors of this article.

Common benign chronic vulvar conditions include genitourinary syndrome of menopause (formerly called vulvovaginal atrophy), lichen sclerosus, lichen planus, lichen simplex chronicus, and vulvodynia. Genitourinary syndrome of menopause results from the hypoestrogenic state that leads to atrophy of normal vulvar and vaginal tissues. It is typically treated with lubricants, moisturizers, and intravaginal estrogen. Lichen sclerosus is an inflammatory condition characterized by intense vulvar itching. It is treated with topical steroids or, in some cases, topical calcineurin inhibitors. Patients with lichen sclerosus are at risk of vulvar squamous cell carcinoma and should be monitored closely for malignancy. Lichen planus is an inflammatory autoimmune disorder that can affect the vulva and vagina in addition to other skin and mucosal surfaces. The first-line treatment is topical steroids, and significant scarring can occur if left untreated. Lichen simplex chronicus manifests as persistent itching and scratching of the vulvar skin that leads to thickened epithelium. Breaking the itch-scratch cycle, often with topical steroids, is the key to treatment. Vulvodynia is a common vulvar pain disorder and is a diagnosis of exclusion. A multimodal treatment approach typically includes vulvar hygiene, physical therapy, psychosocial interventions, and antineuropathy medications.

Benign chronic vulvar conditions are regularly treated in primary care settings.1 This review discusses several of the most common of these conditions.2

SORT: KEY RECOMMENDATIONS FOR PRACTICE

A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, go to https://www.aafp.org/afpsort.

Genitourinary Syndrome of Menopause

Genitourinary syndrome of menopause (GSM), formerly called vulvovaginal atrophy, is a constellation of symptoms associated with changes in vulvar and lower urinary tract anatomy due to menopause-related decreases in levels of estrogen and other hormones. Vaginal dryness and other GSM symptoms are thought to occur in approximately 50% of individuals within three years after the onset of menopause.3

PRESENTATION

Symptoms of GSM include vaginal or vulvar dryness, burning, itching, dyspareunia, bleeding, vaginal discharge, urinary urgency, and recurrent urinary tract infections. These symptoms are not often reported to physicians,4 so proactive questioning should be used to elicit whether they are present (e.g., “Do you have any questions about sex you would like to discuss today?” “Have you noticed any symptoms like vaginal pain or burning recently?”).

Although patients with GSM are by definition postmenopausal, anyone experiencing a hypoestrogenic state may have symptoms of GSM, including those who are breastfeeding, who have central (hypothalamic) amenorrhea, or who are taking medications with antiestrogenic effects (e.g., raloxifene [Evista], tamoxifen, and other selective estrogen receptor modulators; gonadotropin-releasing hormone agonists; aromatase inhibitors).

DIAGNOSIS

On examination, the vulvar epithelium of patients with GSM is typically thin, pale, and/or erythematous. Other signs include loss of vaginal rugae, introital narrowing, decreased tissue elasticity, urethral caruncle, and mucosal prolapse; resorption of the labia minora also may be apparent5 (Figure 1). Diagnosis can be made clinically based on physical examination findings alone. If litmus paper is available, the vaginal pH in untreated postmenopausal patients will be greater than 4.5. A biopsy is not required.

FIGURE 1.

Absent rugae, decreased tissue elasticity, loss of vulvar architecture, and phymosis of the clitoral hood characterize genitourinary syndrome of menopause.

TREATMENT

First-line treatment for GSM involves avoidance of irritants, the use of vaginal moisturizers one to three times per week, and the use of vaginal lubricants during intercourse. However, these measures are often insufficient to resolve symptoms. If further treatment is needed, low-dose intravaginal estrogen therapy is preferred.68 Vaginal estrogen is available in the form of creams, vaginal tablets, or a vaginal ring; all are acceptable for the treatment of GSM8 (Table 1). Local estrogen administration is safe, effective, and proven to improve symptoms of atrophy and to prevent development of recurrent urinary tract infections.6,7

TABLE 1. Vaginal Estrogen Preparations and Recommended Dosing

PreparationCommon formulationsDosing
Vaginal creams
Conjugated estrogen (Premarin)0.625 mg per 1 g of creamApply 0.5 to 2 g of cream intravaginally once per day for 21 days, then stop for seven days or apply 0.5 g intravaginally twice per week (generally start with 0.5-g dose)
Estradiol (Estrace)100 mcg per 1 g of creamApply 0.5 to 4 g of cream intravaginally once per day for two weeks, then reduce to 0.5 g twice per week
Vaginal tablet
Estradiol (Imvexxy, Vagifem, Yuvafem)Vagifem and Yuvafem: 10 mcg per tablet
Imvexxy: 4 or 10 mcg per tablet
Insert tablet into vagina once per day for two weeks, then reduce to twice per week
Vaginal ring
Estradiol (Estring)2-mg ring, released as 7.5 mcg per day over 90 daysInsert ring into vagina; replace every 90 days

Although vaginal estrogen has minimal systemic absorption; does not increase the risk of breast cancer, endometrial cancer, or venous thromboembolism9,10; and does not require concurrent use of progesterone for patients with an intact uterus, patients and physicians still may wish to avoid estrogen. This is often the case with patients who have a history of hormone-sensitive cancer, and it is good practice to consult the patient's oncologist before prescribing any hormonal medication for patients who have had breast cancer.

Alternatives to vaginal estrogen include intravaginal prasterone (Intrarosa), a synthetic form of dehydroepiandrosterone that is approved by the U.S. Food and Drug Administration (FDA) for the treatment of dyspareunia in postmenopausal patients. Prasterone also may be considered for treatment of other GSM symptoms, including moderate to severe vulvovaginal atrophy.11 Ospemifene (Osphena), an oral selective estrogen receptor modulator that is FDA-approved for the treatment of moderate to severe dyspareunia, is also effective for the treatment of vaginal dryness.12

Fractional carbon-dioxide laser therapy creates microabrasions that stimulate blood flow and thicken vaginal tissue. Small studies indicate that it is as effective as vaginal estrogen in treating symptoms of GSM.1316 However, patients should be cautioned that long-term risks of this procedure are not known, and that they should seek treatment only from physicians experienced with this procedure.

Lichen Sclerosus

Lichen sclerosus is a chronic inflammatory dermatitis that typically occurs in the vulvar and anogenital regions. It is associated with autoimmune diseases and hypoestrogenic states such as prepuberty and postmenopause.17,18 The prevalence is estimated to be 1.7%, with an incidence of 14 to 22 cases per 100,000 person-years.1921

PRESENTATION

Patients with lichen sclerosus often experience severe pruritus and dyspareunia. They occasionally report burning, dysuria, or anal discomfort.18

DIAGNOSIS

Lichen sclerosis is characterized by epithelial thinning and inflammation with white, thin plaques on the vulvar skin18 (Figure 222); these plaques commonly occur in a figure-eight configuration involving the perineum and perianal region. Loss of vulvar architecture can occur in advanced disease, in which the labia minora regress and the clitoris becomes scarred or buried beneath the clitoral hood (clitoral phimosis).

FIGURE 2.

Epithelial thinning in lichen sclerosus leads to a “cigarette paper” appearance of the vulva.

Reprinted with permission from O'Connell TX, Nathan LS, Satmary WA, et al. Non-neoplastic epithelial disorders of the vulva. Am Fam Physician. 2008;77(3):322.

The workup for suspected lichen sclerosus involves ruling out other causes of symptoms, including infections. Because patients with lichen sclerosus are at risk of squamous cell carcinoma, a definitive diagnosis should be made with vulvar biopsy.20

TREATMENT

Patients with lichen sclerosus should be treated with a high-potency steroid ointment to alleviate symptoms, prevent architectural damage, and reverse histologic changes.2326 Ointments are generally preferred over creams because of their barrier effects and reduced irritation. Clobetasol 0.05% ointment (Temovate) is most commonly used. It should be applied twice per day until active lesions have regressed (usually about one to two months). After regression, clobetasol can be tapered to one or two times per week for an additional two months, or the patient can be switched to a moderate-potency steroid such as betamethasone 0.1% ointment or other vulvar soothing cream.23

The goal of steroid therapy is to control symptoms and manifestations of disease while using the lowest possible dosage. However, multiple or long courses of topical steroids may be required for patients with lichen sclerosus. Although there are concerns that long-term topical steroid use may cause skin atrophy or irritation and lead to skin breakdown, evidence suggests that there are minimal adverse effects with prolonged or continued use.24 Follow-up visits should occur at least every six months to ensure disease stability. Biopsy should be repeated if worsening or changing lesions are noted, because there is a 4% to 5% risk of vulvar squamous cell carcinoma developing in lichen sclerosus lesions.20,25

If topical steroids are not effective, twice-daily application of a topical calcineurin inhibitor, such as pimecrolimus (Elidel) 1% cream, is an effective alternative.27 Intralesional injections with triamcinolone acetonide (no more than 40 mg across the entire vulva), oral or topical retinoids, oral cyclosporine (Sandimmune), oral methotrexate, oral hydroxyurea (Hydrea), phototherapy, fractional CO2 laser therapy, and mixed methylene blue injections are other options to consider.26,2832

Lichen Planus

Lichen planus is a T cell–mediated inflammatory autoimmune condition affecting the skin and mucosal surfaces.33,34 Its prevalence is estimated at less than 1%, and it most commonly develops between the ages of 40 and 60 years.35

PRESENTATION

Lichen planus can affect any skin or mucosal surface. It often affects more than one part of the body, and many patients with oral manifestations also have genital involvement.36 Common vulvar symptoms include pain, burning, and scarring.

DIAGNOSIS

Physical examination may reveal well-demarcated, bright-red vestibular patches, a hyperkeratotic border, or a net-like plaque known as Wickham striae35 (Figure 322 ). Vulvar architecture may regress, and the vagina is typically affected when there is vulvar involvement.35 The workup involves ruling out other causes, but a definitive diagnosis should be made with biopsy.37

FIGURE 3.

Extensive lichen planus of the vulva with Wickham striae visible at the periphery.

Reprinted with permission from O'Connell TX, Nathan LS, Satmary WA, et al. Non-neoplastic epithelial disorders of the vulva. Am Fam Physician. 2008;77(3):323.

TREATMENT

First-line therapy for lichen planus is similar to that for lichen sclerosus, with twice-daily applications of high-dose steroid ointment (clobetasol 0.05%). Symptoms typically diminish with treatment but rarely resolve completely, often waxing and waning over time.35 The goal of treatment should be to improve symptoms and limit scarring, because eroded surfaces can adhere and lead to synechiae that gradually close the vaginal space. For this reason, intravaginal suppositories of hydrocortisone acetate, 25 mg, are recommended as a symptomatic treatment and to prevent scarring,38 and dilators coated in corticosteroid ointment can be considered for short-term use.

Topical calcineurin inhibitors can be considered for steroid-refractory cases, although frequent recurrence has been reported with this treatment.39,40 Other treatments such as systemic corticosteroids, immune modulators, antifungals, antimetabolites, methotrexate, and oral retinoids have been tried with varied, though often unsuccessful, results.2,41

Lichen Simplex Chronicus

Lichen simplex chronicus (LSC) is a secondary skin disorder that involves lichenification of the vulvar skin due to chronic pruritus and excoriation. LSC is a localized atopic dermatitis in about 65% to 75% of cases and is often associated with allergic conditions such as asthma, hay fever, and eczema.2 Its prevalence is estimated at approximately 0.5%, and it is more common in people older than 60 years and in those with anxiety disorders.42

PRESENTATION AND DIAGNOSIS

The hallmark symptom of LSC is intense pruritus that often disturbs sleep.2 Skin changes are noted on physical examination, including thick leathery skin, pigmentation changes, plaque formation, and excoriations from excessive scratching (Figure 4).22

FIGURE 4.

Thickened, leathery skin in lichen simplex chronicus of the vulva.

Reprinted with permission from O'Connell TX, Nathan LS, Satmary WA, et al. Non-neoplastic epithelial disorders of the vulva. Am Fam Physician. 2008;77(3):324.

TREATMENT

The first step in the treatment of LSC is to consider whether an underlying infection (e.g., candidiasis) or disease (e.g., lichen sclerosus, lichen planus) is causing the intense itching; if so, that condition should be treated first. Avoidance of irritants such as harsh soaps, rough clothing, excessive washing, and daily wear of sanitary pads is also important.

If no underlying condition is identified, the key to therapy is breaking the itch-scratch cycle.2 The use of topical corticosteroids is thought to be the most effective treatment. Moderate-potency formulations (e.g., triamcinolone 0.1% ointment applied twice per day) can be used; a two- to four-week course of a high-potency steroid is another option.43,44 Treatment options for nocturnal itching include the anticholinergics hydroxyzine (starting at a dosage of 25 mg each night) and amitriptyline (25 to 50 mg nightly). These medications should generally be avoided in older adults because of their potential adverse cognitive effects. Systemic corticosteroids or calcineurin inhibitors can be considered for severe refractory cases.43

Vulvodynia

Vulvodynia is vulvar pain without an identifiable cause that persists for at least three months.45 Causes of vulvar pain that should be ruled out include infections (e.g., herpes simplex virus, candidiasis), trauma, neoplasia (e.g., Paget disease, vulvar intraepithelial neoplasia, squamous cell carcinoma), iatrogenic causes (e.g., radiation, chemotherapy, prior surgery), or any of the previously discussed conditions. Although the cause of pain in vulvodynia is not known, it is thought to begin after an inciting event that leads to inflammation and subsequent remodeling of nerve fibers that alters the pain response.45

Vulvodynia can occur alone or in association with another vulvar disorder. Potential comorbidities include interstitial cystitis, fibromyalgia, irritable bowel syndrome, pelvic myofascial pain, psychosocial conditions, and sexual dysfunction.46

PRESENTATION

Pain associated with vulvodynia varies and can be localized, generalized, or mixed; spontaneous or provoked; and intermittent, persistent, constant, immediate, or delayed. The condition is classified as primary (symptoms have always been present) or secondary (symptoms develop after a period of normal function). Vulvodynia is the most common cause of dyspareunia in premenopausal patients.47 Its prevalence is estimated at 12%, but only an estimated one-half of affected individuals seek treatment, and most are incorrectly diagnosed when they do.47

DIAGNOSIS

Diagnosis is based on clinical evaluation after other causes of pain have been ruled out. Physical examination should incorporate pressure point testing using a cotton swab in a circumferential fashion along the vulvar vestibule, which will elicit pain with even light touch in a patient with vulvodynia (Figure 5). Specific neuropathies (e.g., pudendal, ilioinguinal, genitofemoral) should be ruled out.

FIGURE 5.

Pressure point testing for vulvodynia. A cotton swab is used to gently apply pressure at points around the vestibule (similar to a clock face) to determine the location of pain. A positive result is the patient reporting pain or feeling a sharp touch.

TREATMENT

Treatment of vulvodynia begins with simple changes in vulvar hygiene (e.g., avoiding tight clothing, use of mild soaps), stress reduction, pelvic floor physical therapy, and psychosocial interventions such as cognitive behavior therapy or mindfulness-based stress reduction.48 In addition to these physical and psychosocial treatments, a multimodal approach to therapy may include oral medications that alter nerve conduction (e.g., antidepressants, anticonvulsants) and the use of vaginal dilators.48 Topical medications (e.g., lidocaine ointment, estrogen and/or testosterone cream) are not recommended because they have not been proven superior to placebo.49 Vestibulectomy may be necessary in severe cases of localized vulvodynia; when it is performed, patients report improvement in symptoms.48,50

Vulvar Manifestations of Systemic Illness

Dermatologic and systemic conditions such as psoriasis, eczema, and Crohn disease can have vulvar manifestations. Although these conditions are less common causes of vulvar symptoms, they should remain in the differential diagnosis unless another diagnosis is confirmed. Biopsy can rule in or rule out these other conditions and is recommended if the diagnosis is uncertain.43 Table 2 provides a recommended approach to performing vulvar biopsies.

TABLE 2. Tips for Vulvar Biopsy

Use of local anesthetic, such as 2 mL of 1% lidocaine, is recommended before biopsy. Onset of anesthesia is usually two to five minutes after injection.
Punch biopsies are preferred when lesion depth is relevant (e.g., for dermatoses); 3- to 5-mm punch biopsies are usually sufficient.
Hyperpigmented lesions should be biopsied at the thickest portion of the lesion.
Ulcerative lesions should be biopsied at the edge of the lesion bordering normal tissue.
A stitch of fine 3-0 absorbable suture can be used after the biopsy is completed.

This article updates a previous article on this topic by O'Connell, et al.22

Data Sources: A PubMed search was completed in Clinical Queries using the key terms vulvar disorders, vulvar dermatoses, benign vulvar conditions, vulvar pathology, lichen sclerosus, lichen planus, lichen simplex chronicus, genitourinary syndrome of menopause, vulvodynia, vulvar pruritus, and vulvar pain. The search included meta-analyses, randomized controlled trials, clinical trials, and reviews. Also searched were the Cochrane database and the Agency for Healthcare Research and Quality Effective Healthcare Reports. Search dates: September 2, 2019; October 18, 2019; and May 23, 2020.

The authors thank Emory Buck, MD, for research assistance for this article.

NANCY E. RINGEL, MD, is a clinical fellow in the Division of Female Pelvic Medicine and Reconstructive Surgery at Medstar Health, Washington, D.C., and an instructor in the Department of Obstetrics and Gynecology at Georgetown University School of Medicine, Washington, D.C.

CHERYL IGLESIA, MD, is director of the Division of Female Pelvic Medicine and Reconstructive Surgery at Medstar Health and a professor in the Department of Obstetrics and Gynecology and the Department of Urology at Georgetown University School of Medicine.

Published online July 24, 2020.

Address correspondence to Nancy E. Ringel, MD, Georgetown University School of Medicine, 110 Irving St. NW, Ste. 5B-45, Washington, DC 20010. Reprints are not available from the authors.

Author disclosure: No relevant financial affiliations.

  1. 1.Nunns D, Mandal D. The chronically symptomatic vulva: prevalence in primary health care. Genitourin Med. 1996;72(5):343-344.
  2. 2.ACOG practice bulletin no. 93: diagnosis and management of vulvar skin disorders. Obstet Gynecol. 2008;111(5):1243-1253.
  3. 3.Parish SJ, Nappi RE, Krychman ML, et al. Impact of vulvovaginal health on postmenopausal women: a review of surveys on symptoms of vulvovaginal atrophy. Int J Womens Health. 2013;5:437-447.
  4. 4.Krychman M, Graham S, Bernick B, et al. The Women's EMPOWER survey: women's knowledge and awareness of treatment options for vulvar and vaginal atrophy remains inadequate. J Sex Med. 2017;14(3):425-433.
  5. 5.Portman DJ, Gass ML Vulvovaginal Atrophy Terminology Consensus Conference Panel. Genitourinary syndrome of menopause: new terminology for vulvovaginal atrophy from the International Society for the Study of Women's Sexual Health and the North American Menopause Society. Menopause. 2014;21(10):1063-1068.
  6. 6.Rahn DD, Carberry C, Sanses TV, et al.; Society of Gynecologic Surgeons Systematic Review Group. Vaginal estrogen for genitourinary syndrome of menopause: a systematic review. Obstet Gynecol. 2014;124(6):1147-1156.
  7. 7.Ferrante KL, Wasenda EJ, Jung CE, et al. Vaginal estrogen for the prevention of recurrent urinary tract infection in postmenopausal women: a randomized clinical trial [published online June 19, 2019]. Female Pelvic Med Reconstr Surg. Accessed March 27, 2020. https://journals.lww.com/jpelvicsurgery/Abstract/9000/Vaginal_Estrogen_for_the_Prevention_of_Recurrent.99478.aspx
  8. 8.Lethaby A, Ayeleke RO, Roberts H. Local oestrogen for vaginal atrophy in postmenopausal women. Cochrane Database Syst Rev. 2016(8):CD001500.
  9. 9.Crandall CJ, Hovey KM, Andrews CA, et al. Breast cancer, endometrial cancer, and cardiovascular events in participants who used vaginal estrogen in the Women's Health Initiative Observational Study. Menopause. 2018;25(1):11-20.
  10. 10.Chambers LM, Herrmann A, Michener CM, et al. Vaginal estrogen use for genitourinary symptoms in women with a history of uterine, cervical, or ovarian carcinoma. Int J Gynecol Cancer. 2020;30(4):515-524.
  11. 11.Labrie F, Archer DF, Martel C, et al. Combined data of intravaginal prasterone against vulvovaginal atrophy of menopause. Menopause. 2017;24(11):1246-1256.
  12. 12.Archer DF, Goldstein SR, Simon JA, et al. Efficacy and safety of ospemifene in postmenopausal women with moderate-to-severe vaginal dryness: a phase 3, randomized, double-blind, placebo-controlled, multicenter trial. Menopause. 2019;26(6):611-621.
  13. 13.Paraiso MFR, Ferrando CA, Sokol ER, et al. A randomized clinical trial comparing vaginal laser therapy to vaginal estrogen therapy in women with genitourinary syndrome of menopause: the VeLVET trial. Menopause. 2020;27(1):50-56.
  14. 14.Sokol ER, Karram MM. Use of a novel fractional CO2 laser for the treatment of genitourinary syndrome of menopause: 1-year outcomes. Menopause. 2017;24(7):810-814.
  15. 15.Filippini M, Luvero D, Salvatore S, et al. Efficacy of fractional CO2 laser treatment in postmenopausal women with genitourinary syndrome: a multicenter study. Menopause. 2020;27(1):43-49.
  16. 16.Knight C, Logan V, Fenlon D. A systematic review of laser therapy for vulvovaginal atrophy/genitourinary syndrome of menopause in breast cancer survivors. Ecancermedicalscience. 2019;13:988.
  17. 17.Kreuter A, Kryvosheyeva Y, Terras S, et al. Association of autoimmune diseases with lichen sclerosus in 532 male and female patients. Acta Derm Venereol. 2013;93(2):238-241.
  18. 18.Virgili A, Borghi A, Toni G, et al. Prospective clinical and epidemiologic study of vulvar lichen sclerosus: analysis of prevalence and severity of clinical features, together with historical and demographic associations. Dermatology. 2014;228(2):145-151.
  19. 19.Goldstein AT, Marinoff SC, Christopher K, et al. Prevalence of vulvar lichen sclerosus in a general gynecology practice. J Reprod Med. 2005;50(7):477-480.
  20. 20.Bleeker MC, Visser PJ, Overbeek LI, et al. Lichen sclerosus: incidence and risk of vulvar squamous cell carcinoma. Cancer Epidemiol Biomarkers Prev. 2016;25(8):1224-1230.
  21. 21.Halonen P, Jakobsson M, Heikinheimo O, et al. Incidence of lichen sclerosus and subsequent causes of death: a nationwide Finnish register study. BJOG. 2020;127(7):814-819.
  22. 22.O'Connell TX, Nathan LS, Satmary WA, et al. Non-neoplastic epithelial disorders of the vulva. Am Fam Physician. 2008;77(3):321-326. Accessed March 27, 2020. https://www.aafp.org/afp/2008/0201/p321.html
  23. 23.Ference JD, Last AR. Choosing topical corticosteroids. Am Fam Physician. 2009;79(2):135-140. Accessed March 27, 2020. https://www.aafp.org/afp/2009/0115/p135.html
  24. 24.Dalziel KL, Wojnarowska F. Long-term control of vulval lichen sclerosus after treatment with a potent topical steroid cream. J Reprod Med. 1993;38(1):25-27.
  25. 25.Lee A, Bradford J, Fischer G. Long-term management of adult vulvar lichen sclerosus: a prospective cohort study of 507 women. JAMA Dermatol. 2015;151(10):1061-1067.
  26. 26.Kirtschig G, Becker K, Günthert A, et al. Evidence-based (S3) guideline on (anogenital) lichen sclerosus. J Eur Acad Dermatol Venereol. 2015;29(10):e1-e43.
  27. 27.Chi CC, Kirtschig G, Baldo M, et al. Topical interventions for genital lichen sclerosus. Cochrane Database Syst Rev. 2011(12):CD008240.
  28. 28.Ventolini G, Swenson KM, Galloway ML. Lichen sclerosus: a 5-year follow-up after topical, subdermal, or combined therapy. J Low Genit Tract Dis. 2012;16(3):271-274.
  29. 29.Li Z, Wang Y, Wang J, et al. Evaluation of the efficacy of 5-aminolevulinic acid photodynamic therapy for the treatment of vulvar lichen sclerosus. Photodiagnosis Photodyn Ther. 2020;29:101596.
  30. 30.Balchander D, Nyirjesy P. Fractionated CO2 laser as therapy in recalcitrant lichen sclerosus. J Low Genit Tract Dis. 2020;24(2):225-228.
  31. 31.Pagano T, Conforti A, Buonfantino C, et al. Effect of rescue fractional microablative CO2 laser on symptoms and sexual dysfunction in women affected by vulvar lichen sclerosus resistant to long-term use of topic corticosteroid: a prospective longitudinal study. Menopause. 2020;27(4):418-422.
  32. 32.Li Y, Shi J, Tan W, et al. Prospective observational study of the efficacy of mixed methylene blue compound injection for treatment of vulvar non-neoplastic epithelial disorders. Int J Gynaecol Obstet. 2020;148(2):157-161.
  33. 33.Cooper SM, Ali I, Baldo M, et al. The association of lichen sclerosus and erosive lichen planus of the vulva with autoimmune disease: a case-control study. Arch Dermatol. 2008;144(11):1432-1435.
  34. 34.Baldo M, Bailey A, Bhogal B, et al. T cells reactive with the NC16A domain of BP180 are present in vulval lichen sclerosus and lichen planus. J Eur Acad Dermatol Venereol. 2010;24(2):186-190.
  35. 35.Kennedy CM, Galask RP. Erosive vulvar lichen planus: retrospective review of characteristics and outcomes in 113 patients seen in a vulvar specialty clinic. J Reprod Med. 2007;52(1):43-47.
  36. 36.Belfiore P, Di Fede O, Cabibi D, et al. Prevalence of vulval lichen planus in a cohort of women with oral lichen planus: an interdisciplinary study. Br J Dermatol. 2006;155(5):994-998.
  37. 37.Day T, Wilkinson E, Rowan D, et al.; ISSVD Difficult Pathologic Diagnoses Committee. Clinicopathologic diagnostic criteria for vulvar lichen planus. J Low Genit Tract Dis. 2020;24(3):317-329.
  38. 38.Anderson M, Kutzner S, Kaufman RH. Treatment of vulvovaginal lichen planus with vaginal hydrocortisone suppositories. Obstet Gynecol. 2002;100(2):359-362.
  39. 39.Byrd JA, Davis MD, Rogers RS. Recalcitrant symptomatic vulvar lichen planus: response to topical tacrolimus. Arch Dermatol. 2004;140(6):715-720.
  40. 40.Lonsdale-Eccles AA, Velangi S. Topical pimecrolimus in the treatment of genital lichen planus: a prospective case series. Br J Dermatol. 2005;153(2):390-394.
  41. 41.Cline A, Cuellar-Barboza A, Jorizzo JL, et al. Methotrexate for the treatment of recalcitrant erosive lichen planus of the vulva. JAMA Dermatol. 2020;156(2):215-217.
  42. 42.Liao YH, Lin CC, Tsai PP, et al. Increased risk of lichen simplex chronicus in people with anxiety disorder: a nationwide population-based retrospective cohort study. Br J Dermatol. 2014;170(4):890-894.
  43. 43.van der Meijden WI, Boffa MJ, Ter Harmsel WA, et al. 2016 European guideline for the management of vulval conditions. J Eur Acad Dermatol Venereol. 2017;31(6):925-941.
  44. 44.Juarez MC, Kwatra SG. A systematic review of evidence based treatments for lichen simplex chronicus [published online March 6, 2020]. J Dermatolog Treat. Accessed May 29, 2020. https://www.tandfonline.com/doi/full/10.1080/09546634.2019.1708856
  45. 45.Bornstein J, Goldstein AT, Stockdale CK, et al.; Consensus Vulvar Pain Terminology Committee of the International Society for the Study of Vulvovaginal Disease (ISSVD), the International Society for the Study of Women's Sexual Health (ISSWSH), and the International Pelvic Pain Society (IPPS).. 2015 ISSVD, ISSWSH and IPPS consensus terminology and classification of persistent vulvar pain and vulvodynia. Obstet Gynecol. 2016;127(4):745-751.
  46. 46.Lamvu G, Nguyen RH, Burrows LJ, et al. The Evidence-Based Vulvodynia Assessment Project: a national registry for the study of vulvodynia. J Reprod Med. 2015;60(5–6):223-235.
  47. 47.Reed BD, Harlow SD, Sen A, et al. Prevalence and demographic characteristics of vulvodynia in a population-based sample. Am J Obstet Gynecol. 2012;206(2):170.e1-9.
  48. 48.Lamvu G, Alappattu M, Witzeman K, et al. Patterns in vulvodynia treatments and 6-month outcomes for women enrolled in the National Vulvodynia Registry–an exploratory prospective study. J Sex Med. 2018;15(5):705-715.
  49. 49.Miranda Varella Pereira G, Soriano Marcolino M, Silveira Nogueira Reis Z, et al. A systematic review of drug treatment of vulvodynia: evidence of a strong placebo effect. BJOG. 2018;125(10):1216-1224.
  50. 50.Das D, Davidson ERW, Walters M, et al. Patient-centered outcomes after modified vestibulectomy. Obstet Gynecol. 2020;135(1):113-121.

Copyright © 2026 by the American Academy of Family Physicians.

This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. See permissions for copyright questions and/or permission requests.