Pruritus vulvae


Evidence Levels: A Double-blind study B Clinical trial ≥ 20 subjects C Clinical trial < 20 subjects D Series ≥ 5 subjects E Anecdotal case reports

Pruritus vulvae is the external sensation of itching that results in a need to scratch or rub the vulva. Although pruritus vulvae is a common complaint, the etiopathogenesis remains poorly understood. Primary findings are representative of underlying disease processes and may include macular or papular erythema, dyspigmentation, edema, vesicles, and bullae. Secondary findings include atrophy, lichenification, erosions, fissures, excoriations/scarring, and pigmentary changes; scale is rarely seen due to the inherently moist environment. Vaginal discharge is not necessarily associated and may reflect the normal underlying physiologic state. Pruritus vulvae may be primary (essential), secondary, or multifactorial. Regardless of etiology, longstanding pruritus vulvae may result in lichen simplex chronicus. Primary pruritus vulvae is the condition in which no etiology can be identified and will be the focus of this chapter.

Management Strategy

Pruritus vulvae describes a symptom that may be psychologically distressing, socially embarrassing, and detrimental to sexual health and function. Identifying all etiologies is critical to management. Secondary pruritus vulvae may be caused by anatomic alteration, infection/infestation, inflammatory dermatosis, neoplasm, systemic disease, or neurologic dysfunction ( Table 207.1 ). The role of radiculopathies or pudendal nerve entrapment as a cause of vulvar pruritus is increasingly recognized. Furthermore, vulvar pain (vulvodynia) may be difficult to distinguish from vulvar pruritus and is often comorbid. It should be noted that diabetes mellitus, an increasingly common diagnosis worldwide, may contribute to vulvar pruritus through various pathogeneses, including frequent/persistent candidiasis, neuropathic pain, autonomic dysfunction, and primary pruritus. In the absence of any secondary cause of pruritus, the condition is considered primary until proven otherwise.

Table 207.1
Differential diagnosis of pruritus vulvae
Anatomic alterations

  • Fox–Fordyce disease (apocrine duct occlusion)

  • Low-estrogen states

    • Prepuberty

    • Postpartum/lactation

    • Peri- and postmenopause

Infections and infestations

  • Bacterial

    • Group A β-hemolytic streptococcus

    • Group B β-hemolytic streptococcus

    • Staphylococcus aureus

    • Chlamydia trachomatis

    • Erythrasma

    • Gardnerella vaginalis

    • Neisseria gonorrhoeae

    • Mycobacterium tuberculosis

  • Fungal

    • Candida albicans

    • Candida glabrata (non-albicans candidiasis)

    • Tinea cruris

  • Infestation

    • Enterobius vermicularis (pinworm)

    • Phthirus pubis (pubic lice)

    • Sarcoptes scabiei

    • Trichomonas vaginalis

  • Viral

    • Herpes simplex virus

    • Human papillomavirus

    • Human immunodeficiency virus

    • Molluscum contagiosum

Inflammatory dermatoses

  • Allergic contact dermatitis

  • Atopic dermatitis

  • Dermatographism

  • Desquamative inflammatory vaginitis

  • Fixed drug eruption

  • Hidradenitis suppurativa

  • Irritant contact dermatitis

  • Leukoplakia of unknown etiology

  • Lichen planus

  • Lichen sclerosus

  • Lichen simplex chronicus

  • Papular acantholytic dyskeratosis (Grover disease)

  • Psoriasis

  • Seborrheic dermatitis

  • Zoon (plasma cell) vulvitis

Neoplasms

  • Basal cell carcinoma

  • Epidermolytic acanthoma

  • Extramammary Paget disease

  • Hidradenoma papilliferum

  • Langerhans cell histiocytosis

  • Lymphoma

  • Melanoma

  • Squamous cell carcinoma

  • Squamous cell carcinoma in situ (Bowen disease, vulvar intraepithelial neoplasia)

  • Syringoma

Systemic diseases

  • Crohn disease

  • Diabetes mellitus

  • Hepatic failure

  • Hypothyroidism

  • Iron-deficiency anemia

  • Polycythemia vera

  • Renal failure

  • Sjögren syndrome

Neurologic

  • Fibromyalgia

  • Postherpetic neuralgia

  • Pudendal nerve entrapment

  • Vulvodynia

A thorough history is the first step in understanding all possible etiologies of pruritus vulvae in a given patient. A personal or family history of any inflammatory dermatosis may direct the differential diagnosis. Any history of self-directed treatment should be elicited. In addition, a complete mucocutaneous examination should be performed with attention to primary and secondary findings. This should entail visual and manual inspection of the vulva, vagina, and perianal skin and the complete mucocutaneous integument (i.e., the oral cavity, conjunctivae, and nasal mucosa, as well as a total body skin, scalp, and nails examination). In conducting the genital exam, it is vital to distinguish normal vulvar anatomy (which varies widely) from any pruritus-associated pathology. Special care should be given to distinguish physiologic pigmentation from associated erythema, inflammation, or infiltrative process in vulvar skin, regardless of skin tone. In skin of color, clinical findings can vary from pink to tan to violaceous or hyperpigmented lesions. The clinician should also preform palpation of inguinal lymph nodes and sensory testing for light touch of the vulva and vaginal vestibule. Utilizing current International Society for the Study of Vulvovaginal Disease (ISSVD) terminology to classify dermatologic findings is useful in forming a differential. A number of specific investigations may further aid in diagnosis.

Specific Investigations

  • Saline wet mount with cytologic evaluation of keratinocytes, inflammatory cells

  • KOH whiff test

  • Wood’s lamp or KOH preparation

  • Vaginal pH

  • Scotch tape test

  • Microbial assays

  • Laboratory values to identify systemic conditions (i.e., diabetes, liver disease)

  • Patch testing

  • Vulvoscopy

  • Colposcopy

  • Nerve conduction studies

Upon identification of any primary or secondary etiologies, appropriate treatment should be instituted. If no etiology is identified (primary pruritus vulvae), then symptomatic relief is the goal of therapy. The tenets of treatment are to interrupt the itch–scratch cycle, restore the skin barrier, and minimize impact on quality of life. The critical first step is to identify and remove all suspected local irritants and allergens . The patient should be counseled to institute a number of lifestyle modifications ( Table 207.2 ). The patient may resist some measures, particularly the avoidance of fragranced or ‘cleansing’ products, due to desire for a ‘clean’ vulva and vagina; they may believe natural secretions and odors are offensive or even the cause of their symptoms. To the contrary, elaborate hygiene regimens contribute to local irritation and contact sensitivity and may confound or be the primary cause of persistent pruritus. Talc in particular is highly irritating, and investigation of its role in ovarian cancer remains inconclusive. Whenever possible, systemic rather than local preparations should be used in the treatment of pruritus to limit concurrent secondary irritation. However, it has also been reported that ingested food and drug metabolites excreted in urine and stool can serve as allergens and/or irritants, contributing to anogenital pruritus.

Table 207.2
Lifestyle modifications in the management of pruritus vulvae
Avoid all local products, including soaps, personal hygiene products, moisturizers, and medications not approved by a dermatologist
Bathe with lukewarm (not hot) water
Pat (not rub) the genital area to dry
Minimize pubic grooming (waxing, shaving)
Cool Sitz baths may help symptoms
Avoid occlusive, tight, and/or synthetic clothing items
Launder clothing using a double rinse cycle
Use cotton (or cotton-lined) underwear and washcloths. Change daily
Menstrual management products must be fragrance-free and changed with appropriate frequency. Silicone menstrual cups or reusable cloth pads may provide less irritation than traditional paper-based products
Avoid wipes and use only the required amount of toilet paper as these items may contribute to local irritation
Wipe gently front-to-back to limit inadvertent introduction of secretions to vagina or vestibule. Urine, stool, sweat, semen, and cervical or vaginal secretions contribute to irritation
Urinary incontinence and contact with stool should be thoroughly addressed with a healthcare provider

Maintenance of barrier function facilitates healing and limits irritant contact. The use of petrolatum- and zinc-based ointments helps to seal in moisture and protect the affected skin from external chemical and physical insults. Ointments generally contain fewer inactive ingredients, thus limiting potential irritants or allergens. In low-estrogen states, the use of topical or systemic estrogen helps restore vaginal and vulvar mucosal barrier function.

Corticosteroids are used to reduce inflammation. Corticosteroid ointment should be used sparingly once or twice a day. Close clinical supervision is necessary to identify and mitigate adverse effects (e.g., striae, folliculitis, atrophy). Intralesional (injected) and systemic corticosteroids may be effective for recalcitrant pruritus. Non-inflammatory idiopathic disease does not benefit from topical corticosteroids. When topical steroid does not alleviate symptoms, other etiologies must be considered.

Corticosteroids reduce pruritus but are often insufficient to interrupt the itch–scratch cycle. Antihistamines such as hydroxyzine or topical doxepin are recommended for night-time therapy. For daytime pruritus, a low-dose selective serotonin reuptake inhibitor is advised. Amitriptyline , pregabalin , or gabapentin may be effective in pruritus characterized by pain, burning, or stinging sensations. Local anesthetics such as lidocaine 2% jelly may be used to facilitate intercourse or otherwise provide temporary relief.

Numerous investigative treatments for specific genital conditions have shown relief of pruritus and may be indicated off-label. The systemic immunotherapy ixekizumab (an interleukin-17A inhibitor) has been shown to significantly improve itch in patients with genital psoriasis. Dupilumab (an interleukin-4 receptor α-blocker) was effective in a case of recalcitrant anogenital pruritus in a male. Innovative therapies, including phototherapy, platelet-rich plasma, and adipose-derived stem cells, have shown promise in specific pruritic conditions (such as lichen sclerosus) and may be considered in the future for primary pruritus vulvae.

Ultimately, management of pruritus vulvae requires that providers display utmost empathy and compassion. Difficulties in diagnosis and treatment can be exhausting and frustrating for affected patients. It is important to assess subjective impact of the condition on the patient’s mental health and functional status and refer for supportive therapy as needed. Lifestyle changes and specific therapies should be adopted through shared decision-making.

First-Line Therapies

  • Avoidance of irritants

  • E

  • Good hygiene practices

  • E

  • Oral ospemifene

  • A

  • Topical estrogen

  • E

  • Amitriptyline, pregabalin, gabapentin

  • C

Effects of ospemifene on genitourinary health assessed by prospective vulvar-vestibular photography and vaginal/vulvar health indices

Goldstein I, Simon JA, Kaunitz AM, et al. Menopause 2019; 26(9): 994–1001.

Pruritus is a significant contributor to postmenopausal morbidity. Ospemifene or deaminohydroxytoremifene is an oral selective estrogen receptor modulator (SERM) FDA-approved for dyspareunia in 2014. A randomized controlled trial of 631 postmenopausal women demonstrated significant improvement of vulvovaginal health with oral ospemifene over placebo, as assessed by visual, objective, and subjective (symptomatic) measures.

Generalized unprovoked vulvodynia; a retrospective study on the efficacy of treatment with amitriptyline, gabapentin or pregabalin

van Beekhuizen HJ, Oost J, van der Meijden WI. Eur J Gynecol Obstet Reprod Biol 2018; 220: 118–21.

A Dutch study of 241 women with vulvodynia (of whom 18% had likely vulvar dermatoses and 83% reported symptoms of itching or burning) showed good response to regimens of amitriptyline, gabapentin, and/or pregabalin. Of women with vulvar dermatoses, 43% experienced a relief in symptoms.

Vaginal symptoms in postmenopausal women: self-reported severity, natural history, and risk factors

Huang AJ, Moore EE, Boyko EJ, et al. Menopause 2010; 17(1): 121–6.

A longitudinal study of 1017 postmenopausal women found that approximately one-third reported vaginal itching at baseline. In the 77 women who reported itching at baseline and no current or subsequent estrogen use, about half had spontaneous resolution of their itch within the 24-month study period.

Second-Line Therapies

  • Topical antihistamine

  • A

  • Subcutaneous triamcinolone

  • B

  • Naltrexone

  • D

An evidence-based review of the efficacy of topical antihistamines in the relief of pruritus

Eschler DC, Klein PA. J Drugs Dermatol 2010; 9(8): 992–7.

Four large, double-blinded, randomized control trials have demonstrated efficacy of topical antihistamines, specifically doxepin, in treating pruritus (note the review was not limited to vulvar pruritus). However, topical applications should be considered thoughtfully in patients at risk for increased local vulvar irritation.

Subcutaneous injection of triamcinolone acetonide in the treatment of chronic vulvar pruritus

Kelly RA, Foster DC, Woodruff JD. Am J Obstet Gynecol 1993; 169: 568–70.

A series of 45 patients with chronic pruritus vulvae were treated with subcutaneous intralesional injection of triamcinolone acetonide (total 15–20 mg). Thirty-five experienced relief of pruritus for more than 1 month (mean 5.8 months).

Treatment of refractory vulvovaginal pruritus with naltrexone, a specific opiate antagonist

Bottcher B, Wildt L. Eur J Obstet Gynecol Reprod Biol 2014; 174: 115–6.

Initial report detailing the rapid and complete response to oral naltrexone 50 mg once daily in five women otherwise healthy with longstanding vulvovaginal pruritus.

Third-Line Therapies

  • Topical corticosteroids

  • A (negative study)

  • Alternative therapies (e.g., Chinese medicine, acupuncture, hypnosis)

  • E

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