AUTHOR AND EDITOR INFORMATION

Section 1 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

INTRODUCTION

Section 2 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

In the last few years, interest in vulvar disease has greatly increased. However, the relevant material has been scattered throughout the literature of various specialties, including dermatology, genitourinary medicine, gynecology, and pathology. The spectrum of involved specialties reflects the complexity of vulvar diseases and the necessity of a multidisciplinary approach in the study of the vulva. In response to the various approaches of the specialists faced with treating vulvar disease, the World Health Organization, the International Society for the Study of Vulvar Disease, the International Federation of Gynecology and Obstetrics, and the International Society of Gynecological Pathologists have made an effort to standardize the nomenclature.

Some general anatomic, embryologic, and histologic findings of the vulva bear review. The vulva is the part of the female genital tract located between the genitocrural folds laterally, the mons pubis anteriorly, and the anus posteriorly. Embryologically, it is the result of the junction of the cloacal endoderm, urogenital ectoderm, and paramesonephric mesodermal layers. This hollow structure contains the labia majora, labia minora, clitoris, vestibule, urinary meatus, vaginal orifice, hymen, Bartholin glands, and Skene ducts. Different epithelia, from keratinized squamous epithelium to squamous mucosa, cover the vulva. The labia minora are rich with sebaceous glands but have few sweat glands and no hair follicles. The epithelium of the vestibule is neither pigmented nor keratinized and contains eccrine glands.

Benign vulvar disorders are a significant issue for patients. These disorders include vulvar atrophy, benign tumors, hamartomas and cysts, infectious disorders, and nonneoplastic epithelial disorders. Infectious disorders include diseases caused by known transmissible agents, such as viruses, bacteria, fungi, and protozoa. They may first be seen by physicians of various specialties, including dermatologists and gynecologists, and often require a multidisciplinary approach.

Developmental abnormalities of vulva are generally rare. Vulvar atrophy may be related to advanced age or other disorders, but these abnormalities often represent an almost physiological finding in the elderly.

Benign tumors of the vulva are relatively uncommon and may show nonspecific clinical features. Therefore, a biopsy is often needed to exclude a malignant neoplasm and to indicate proper treatment. Vascular neoplasms may also occur in the vulva and are similar to such lesions found elsewhere.

Nonneoplastic epithelial disorders include several inflammatory, ulcerative, and blistering disorders, as well as pigmentary changes involving the vulvar region.

Benign vulvar diseases

Nonneoplastic epithelial disorders

• Inflammatory diseases
• • Lichen sclerosus
  • Squamous cell hyperplasia (with and without atypia)
  • Lichen simplex chronicus (localized neurodermatitis)
  • Primary irritant dermatitis
  • Intertrigo
  • Allergic contact dermatitis
  • Fixed drug eruption
  • Erythema multiforme
  • Toxic epidermal necrolysis
  • Atopic dermatitis
  • Seborrheic dermatitis
  • Psoriasis
  • Reiter disease
  • Lichen planus
  • Lupus erythematosus
  • Darier disease
  • Aphthosis and Behçet disease
  • Pyoderma gangrenosum
  • Crohn disease
  • Hidradenitis suppurativa
  • Fox-Fordyce disease
  • Plasma cell vulvitis
  • Vulvar vestibulitis syndrome
• Blistering diseases
• • Familial benign chronic pemphigus (Hailey-Hailey disease)
  • Bullous pemphigoid
  • Cicatricial pemphigoid
  • Pemphigus vulgaris
  • Erythema multiforme
  • Epidermolysis bullosa
• Pigmentary changes
• • Acanthosis nigricans
  • Lentigo, lentiginosis, and benign vulvar melanosis
  • Melanocytic nevus
  • Postinflammatory hyperpigmentation
  • Postinflammatory hypopigmentation
  • Vitiligo
•  Benign tumors, hamartomas, and cysts
• • Mucous cysts
  • Bartholin and Skene duct cysts
  • Epidermal inclusion cyst
  • Seborrheic keratosis
  • Acrochordon (fibroepithelial polyp)
  • Fibroma, fibromyoma, and dermatofibroma
  • Lipoma
  • Hidradenoma
  • Hemangioma
  • Lymphangioma
  • Angiokeratoma
  • Pyogenic granuloma
  • Endometriosis
  • Heterotopic sebaceous glands and sebaceous gland hyperplasia
  • Papillomatosis (papillary vulvar hirsutism)
• Congenital malformations
• • Ambiguous external genitalia
  • Congenital labial hypertrophy
  • Labial adhesions
• Atrophy of the vulva

ETIOLOGY AND PATHOPHYSIOLOGY

Section 3 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

Nonneoplastic epithelial disorders

Inflammatory diseases

• Lichen sclerosus
  • The etiology of this condition is unknown. A higher prevalence of the disease in postmenopausal women suggests hormonal factors, but this has not been confirmed.
  • Investigative studies aimed toward identifying an infection-causing agent (eg, spirochetes, viruses) have yielded inconclusive results.
  • Lichen sclerosus has been weakly linked to autoimmune diseases and genetic factors.
  • The role of local factors (eg, trauma, friction, chronic infection and irritation) is well recognized, and recurrence near vulvectomy scars has been observed.
• Squamous cell hyperplasia
  • Repetitive scratching or rubbing from irritants can result in squamous cell hyperplasia. Because this condition is often thought to be equivalent to lichen simplex chronicus, some diagnostic confusion exists.
  • Ambiguous and even inexplicable terms, such as atypical epithelial hyperplasia (dysplasia), vulvar dystrophy, vulvar atypia, atrophic dystrophy, mixed dystrophy, and vulvar intraepithelial neoplasia, inhibit effective communication between clinicians and pathologists. These terms have different meanings to dermatologists, pathologists, and gynecologists, further complicating the problem.
• Lichen simplex chronicus (localized neurodermatitis)
  • Lichen simplex chronicus of the vulva is the end stage of the itch-scratch-itch cycle. The initial stimulus to itch may be underlying seborrheic dermatitis, intertrigo, tinea, or psoriasis; however, in most cases, the underlying cause is not evident and may have been transient vulvitis or vaginal discharge.
  • Any itching disease of the vulva may become secondarily lichenified.
• Primary irritant dermatitis
  • In the absence of any immune reactivity, this condition is a common cause of vulvar burning and pruritus due to irritation.
  • Chemical agents that remove surface lipids, denature epidermal keratins, or damage cell membranes with a direct cytotoxic effect on cells may cause irritation.
  • Common irritants include perfumed soaps and detergents, fabric softeners, feminine hygiene products (eg, tampons, pads, diapers, wipes, deodorant sprays), bubble baths, bath oils, colored or scented toilet paper, physically abrasive contactants (eg, face cloths, sponges), and body secretions (eg, urine, semen).
  • Obsessive cleaning of the vulvar area may also cause serious irritation.
  • Irritation may eventually arise as a result of friction from tight clothing, trapping of moisture due to lack of ventilation (eg, from wearing synthetic fabrics), or activities such as bicycling and horseback riding.
• Intertrigo: This condition is a nonspecific inflammatory eruption of skin folds that can be precipitated by sweating, obesity, and occlusion.
• Allergic dermatitis
  • Vulvar allergic dermatitis may occur as a result of a delayed, cell-mediated, type IV hypersensitivity reaction. An inflammatory disorder originating from local contact with an agent to which the patient has previously been sensitized, vulvar allergic dermatitis develops 12-48 hours after exposure. Less commonly, vulvar pruritus may coincide with more generalized allergic symptoms. Known allergens include topical medications and various chemicals in products such as perfumes, preservatives, and latex. Nickel sensitivity from snaps or zippers in denim jeans or undergarments may also occur.
  • Topical allergens in vulvar allergic dermatitis include the following:
    • Antibiotics - Neomycin, clindamycin, tetracycline, sulfonamides, nifuratel
    • Anesthetics - Benzocaine, lidocaine, prilocaine, pramoxine
    • Antihistamines - Promethazine, diphenylenediamine hydrochloride, p-phenylenediamine, ethylenediamine dihydrochloride
    • Antiseptics - Hexachlorophene
    • Clothing dyes
    • Moisturizers - Lanolin
    • Nail polish
    • Nickel
    • Plants - Poison ivy
    • Preservatives - Paraben, imidazolidinyl urea
    • Perfumes - Balsam of Peru
    • Rubber - Gloves, condoms, diaphragms
• Fixed drug eruption
  • A fixed drug eruption is a cell-mediated allergic drug reaction typically recurring in the same site upon reexposure.
  • Common causative agents include oral drugs such as nonsteroidal anti-inflammatory agents, acetaminophen, sulfonamides, tetracycline, and barbiturates.
• Atopic dermatitis
  • Atopic dermatitis usually occurs in patients with a personal or family history of asthma, hay fever, childhood eczema, or dry skin and is related to a cutaneous hypersensitivity associated with defective cell-mediated immunity and immunoglobulin E overproduction.
  • Although airborne and food allergens may generally play a role, because of their skin hypersensitivity, atopic individuals sometimes show vulvar symptoms as a result of irritation by personal hygiene products (eg, soaps, cleansers, lotions, perfumes, sanitary napkins).
• Seborrheic dermatitis
  • The cause of seborrheic dermatitis is unknown. Seborrhea is evidently a substantial predisposing factor because lesions occur in areas of the skin where sebaceous glands are most active, such as the face, scalp, body folds, and, less commonly, the genitalia.
  • Seborrheic dermatitis is commonly observed in neonates during the first trimester (as a result of sebaceous gland activation by maternal androgens) or after puberty.
  • An association with Pityrosporum yeasts has been noted.
  • Neurological factors have also been thought to play a role; emotional stress, Parkinson disease, nerve injury, and syringomyelia have been related to onset or worsening of the disease.
  • Seasonal factors, zinc deficiency, and HIV infection have been linked to this disorder.
• Psoriasis
  • This common condition is a hereditary disorder of the skin that affects approximately 2% of the population in the Western world. The characteristic silver-white scales on erythematous plaques are caused by rapid cell turnover and primarily occur in sites of repetitive trauma, such as the scalp, elbows, forearms, knees, hands, and feet.
  • Rarely, vulvar involvement occurs and is sometimes triggered or worsened by local factors such as irritation from scratching, irritant soaps, bacterial or yeast superinfections, or increases in heat and humidity secondary to the use of tight synthetic clothing and sanitary napkins.
• Reiter disease
  • This disease is a sterile oligoarthritis typically associated with conjunctivitis and with a distant infection (eg, Chlamydia trachomatis, Ureaplasma urealyticum, Shigella, Salmonella), causing nongonococcal urethritis or enteritis. Additional findings include palmoplantar keratoderma, circinate balanitis, and, less frequently, vulvar involvement.
  • Eighty percent of Reiter disease patients are HLA-B27 positive. However, the exact role of this major histocompatibility class I antigen in the development of this disease remains unclear.
• Lichen planus
  • Lichen planus can be an acute or chronic dermatosis affecting the skin, mucous membranes, or both. Its cause is unknown, but evidence suggests that it is an immunologically mediated disorder. Some drugs have been found to induce lichen planus–type eruptions.
  • Vulvar lesions may be more common than generally considered; a recent report found genital involvement in 51% of women with cutaneous disease.
• Lupus erythematosus
  • Lupus erythematosus is an idiopathic autoimmune disorder that can affect many organ systems. According to the degree of systemic involvement, the disease is classified into systemic, subacute, chronic, or discoid forms.
  • Genital involvement is uncommon, and vulvar manifestations have seldom been described. In one study, vulvar lesions were found in 2 (5%) of 42 women affected by the chronic form.
• Darier disease
  • Darier disease is a heritable disorder of keratinization transmitted as an autosomal dominant trait. Altered keratinization is a result of the disruption of desmosomal proteins with consequent tonofilament detachment and acantholysis because of the mutation of a gene located on band 12q23-24.1.
  • Genital involvement is frequent and is precipitated by heat, humidity, sweat, and friction.
• Aphthosis
  • Aphthosis is a condition of unknown etiology characterized by single or multiple painful canker sores on the oral and genital mucosa. Synonyms include aphthous ulcers, canker sores (on the vulva), Lipschütz ulcers, and ulcus vulvae acutum.
  • The condition may be associated with autoimmune disease. Premenstrual exacerbations are common.
• Behçet disease
  • Behçet disease is a chronic multisystemic inflammatory disorder characterized by oral and genital aphthous ulcers and ocular involvement.
  • Its etiology is unknown but probably involves altered immunity in genetically predisposed subjects because an association with the expression of some HLAs (B51 and DR4) and a racial predilection for individuals of Asian or Middle Eastern descent have been shown.
• Pyoderma gangrenosum
  • The etiology of this disease is still unknown, although evidence of its etiologic and pathogenic background may be found in its frequent association with systemic autoimmune diseases (eg, Crohn disease, arthritis, monoclonal gammopathy).
  • Moreover, evidence suggests that altered immunity occurs in some patients with pyoderma gangrenosum.
  • Vulvar involvement occurs, albeit rarely, with approximately 8 cases reported in the literature.
• Crohn disease
  • Crohn disease is a chronic granulomatous inflammatory bowel disease that may primarily or secondarily involve the vulvar (2%) and inguinal regions.
  • Proposed causes include an unrecognized infectious agent or a disturbed immunologic reaction to an intestinal organism in a genetically predisposed individual.
• Hidradenitis suppurativa
  • Hidradenitis suppurativa is a chronic suppurative inflammatory disorder of the apocrine glands resulting—as with acne vulgaris and acne mechanica—from acute and chronic follicular occlusion.
  • Several factors, including onset at puberty, female predilection (female-to-male ratio, 3:1), typical flares with menstruation, spontaneous regression at menopause, and occasional association with the use of an oral estroprogestinic, suggest a role for hormonal factors.
  • Familial cases and racial predilection (ie, more common in blacks) indicate that genetic factors may also play a role.
  • Obesity, profuse sweating, and overheating are other precipitating factors.
• Fox-Fordyce disease
  • Fox-Fordyce disease is an uncommon condition of the axillary and anogenital regions related to apocrine sweat duct occlusion and is typically exacerbated by factors that stimulate apocrine secretion.
  • Its cause is unknown. Improvement is observed at menopause, with pregnancy, or following oral contraceptive intake.
• Plasma cell vulvitis: This condition, corresponding to Zoon plasma cell balanitis, has also been reported on the vulva. The etiology is unknown.
• Vulvar vestibulitis
  • The pathogenesis of vulvar vestibulitis is obscure. Studies suggesting a relative inability to down-regulate proinflammatory interleukin-1 beta activity by interleukin-1 receptors need further confirmation.
  • Sexual activity, human papillomavirus infection, bacterial infection, or candidal infections seem to be unlikely factors.
  • Association with sensitization to seminal fluid or with interstitial cystitis may occasionally be found.
  • Altered density of nerve endings and estrogen receptors has been demonstrated.
  • The use of oral contraceptives might be a contributing factor by increasing the sensitivity of the vestibular mucosa.

Blistering diseases

• Familial benign chronic pemphigus (Hailey-Hailey disease)
  • Hailey-Hailey disease is a rare autosomal dominant acantholytic disorder due to a mutation on band 3q21-q24 and is characterized from late adolescence or adulthood by recurrent eruptions of vesicles and blisters typically located on the neck, axillae, and groin.
  • Intrinsic desmosomal fragility may only become evident when trigger factors (eg, friction, infections, irritants, increased temperature and humidity, acute UV exposure) precipitate acantholysis. Because most of these conditions frequently occur in the anogenital area, vulvar problems may be common.
• Bullous pemphigoid
  • Bullous pemphigoid is a blistering autoimmune disorder that usually affects elderly patients.
  • The disorder is caused by antibodies binding 2 different antigens, BPAg1 (230 kd) and BPAg2 (a hemidesmosomal antigen of 180 kd now thought to be collagen XVII), located in the basement membrane of the skin.
  • Mucosal lesions of the vulva occur less frequently and are less severe than other blistering disorders.
  • A juvenile localized subtype of immunoglobulin G (IgG)–mediated bullous pemphigoid occurring in children in the first year of life and characterized by a self-limited nonscarring bullous pemphigoid–like process involving only the vulva has been described.
• Cicatricial pemphigoid
  • Cicatricial pemphigoid is an autoimmune condition with autoantibodies directed against collagen XVII and laminin-5 located in the basement membrane zone. Resulting inflammation and subepidermal splitting leads to typical mucosal scarring.
  • Genital involvement is common and reportedly occurs in at least 50% of patients.
• Pemphigus vulgaris
  • This autoimmune blistering disorder affecting the skin and mucosa is due to circulating autoantibodies directed toward desmoglein III (130 kd), a desmosomal cadherin that mediates cell-to-cell adhesion in the epidermis.
  • The vulva is affected in approximately 10% of cases.
• Erythema multiforme (minor/major)
  • Erythema multiforme is a cutaneous hypersensitivity reaction that may be triggered by herpesvirus infection or drug intake. Sulfonamides, beta-lactam antibiotics, and nonsteroidal anti-inflammatory drugs are the offending agents in most patients.
  • Vulvar involvement is frequently observed in the more severe forms of the disease, along with lesions located on other mucosal (eg, eye, mouth, throat) and skin sites.
• Epidermolysis bullosa
  • This term indicates a group of congenital disorders characterized by skin fragility due to an inherited defect in the epidermal, junctional, or dermal components underlying the physiological mechanical properties of the skin.
  • Mucous membranes, including those of the genitalia, may be involved.

Pigmentary changes

• Acanthosis nigricans
  • Acanthosis nigricans is a diffuse pigmentary change typically observed in intertriginous areas and skin folds. It may be hereditary, drug induced, or associated with obesity or endocrine diseases.
  • It sometimes represents a paraneoplastic syndrome, revealing associated malignant epithelial tumors or lymphoproliferative disorders.
• Lentigo, lentiginosis, and benign vulvar melanosis
  • These conditions, characterized by benign epidermal melanocytic hyperplasia, are the most common pigmented lesions reported to occur in the vulva.
  • Hyperpigmented macules of less than 4 mm in diameter define lentigo, whereas larger macules are usually vulvar melanosis.
  • Lentiginosis is characterized by multiple spots of hyperpigmentation and may sometimes be an expression of a genetic disorder such as Peutz-Jeghers syndrome, LEOPARD syndrome (ie, lentigines, electrocardiographic [conduction abnormalities], ocular [hypertelorism], pulmonary [stenosis], abnormal [genitalia], retardation [of growth], and deafness syndrome), or somatic mosaicism.
• Melanocytic nevus
  • Vulvar nevi are fairly common (0.1% of nevi have this location).
  • The etiology of nevi at other skin sites is still a matter of debate. Nevus cells deriving from the neural crest migrate into the skin during embryogenesis and collect in the basal cell layer of the epidermis, where they proliferate in small nests.
• Postinflammatory hyperpigmentation: This condition is due to melanin deposition in the dermis following a previous inflammatory process caused by drug intake (end stage of a fixed drug eruption) or other dermatological disorders localized to the vulva (eg, lichen planus, discoid lupus erythematosus, psoriasis).
• Postinflammatory hypopigmentation: This condition is due to temporary or permanent melanocyte damage of different causes, including skin injury with scar formation and chronic inflammatory skin diseases (eg, lichen sclerosus, discoid lupus erythematosus).
• Vitiligo: This condition is an acquired loss of pigmentation secondary to possible immunologically mediated melanocyte damage. Genital involvement is common.

Benign tumors, hamartomas, and cysts

• Mucous cysts
  • These are dysontogenetic cysts arising from the minor vestibular glands or from mesonephric duct remnants.
  • A cyst of the canal of Nuck (processus vaginalis peritonei) that fills with peritoneal fluid may also occur.
• Bartholin cyst and Skene duct cyst: These cysts develop as a result of ductal occlusion.
• Epidermal inclusion cyst: This common cystic lesion arises from obstruction of a sebaceous gland.
• Seborrheic keratosis: The etiology of this common pigmented epithelial proliferation is unknown, although it may be inherited.
• Acrochordon: A fibroepithelial polyp (acrochordon) is a skin tag commonly observed in areas subject to irritation.
• Fibroma, fibromyoma, and dermatofibroma: Fibromas and related fibromyomas are the most common benign solid vulvar tumors. Their cause is unknown.
• Lipoma: Lipomas, or fatty tumors, are the second most common solid tumors found in the vulvar area. The etiologies of other benign connective tumors in this area are unknown.
• Hidradenoma: Hidradenomas are benign tumors arising from sweat glands or ducts.
• Hemangioma: Hemangiomas are benign tumors of the vascular endothelium that occur in infants. They enlarge by active proliferation of endothelial cells due to still unknown factors.
• Lymphangioma: Lymphangiomas are benign tumors of the lymphatic vessels that only rarely occur on the vulva. They may be congenital or acquired, and in such cases they may represent a complication of radiation therapy.
• Angiokeratoma: Angiokeratomas of Fordyce are small benign vascular proliferations of unknown cause that are common on hair-bearing skin of the external genitalia (eg, vulva, scrotum). Association with radiotherapy has sometimes been reported.
• Pyogenic granuloma: This type of granuloma is a vascular proliferation of unknown cause; occasionally, pyogenic granulomas are associated with a history of trauma.
• Endometriosis
  • Endometriosis is an uncommon benign neoplasm in the vulva produced by implantation of endometrial fragments, often following trauma or surgical procedures (eg, endometrial curettage, cesarean delivery).
  • Chocolate cysts of this benign metastasizing neoplasm may also be found near the umbilicus.
• Heterotopic sebaceous glands and sebaceous gland hyperplasia
  • Heterotopic sebaceous glands are normal variants and represent the equivalents of Fordyce spots on the oral mucosa.
  • Sebaceous gland hyperplasia is a benign hamartomatous condition commonly observed on the face in elderly patients, but it has also been reported on the vulva.
• Papillomatosis (papillary vulvar hirsutism): Similar to pearly penile papules occurring over the corona and penile sulcus, these papillary growths of vestibular mucosa are normal variants of female anatomy. Their origin is unknown. No association with human papillomavirus infection has been detected so far.

Congenital malformations

• Ambiguous external genitalia
  • Sexual ambiguity is a term used to describe situations in which the external genital organs are not clearly female or male at birth. The 3 main etiologic categories include (1) female pseudohermaphroditism, accounting for 80% of ambiguous genitalia; (2) male pseudohermaphroditism, occurring in approximately 15% of cases; and (3) disorders of differentiation.
  • The preponderance of female pseudohermaphroditism is due to a recessive congenital enzymatic defect of adrenal steroid biosynthesis (most commonly, 21-hydroxylase deficiency), resulting in androgen overproduction that virilizes the external genitalia of a female 46,XX fetus with normal ovaries. Although rare, maternal factors can also virilize a female fetus.
  • In male pseudohermaphroditism, healthy 46,XY infants have a partial or complete block in the masculinization process during development as a result of a lack of gonadotropin, an enzyme defect in testosterone biosynthesis, or a defect in androgen-dependent target tissue response.
  • Differentiation disorders arise from an abnormality of the number or structure of the X and Y chromosomes or of a male-specific transplant antigen that interacts with the Y chromosome to induce testicular differentiation.
• Congenital labial hypertrophy
  • Noted at puberty, hypertrophy of the labia minora is not an uncommon developmental anomaly. The condition is an anatomic variant rather than a malformation.
  • Rarely, it occurs because of lymphostasis or chronic physical pulling on the labia.
• Labial adhesions
  • These adhesions result from fusion of the labia minora and occur in 1.4% of prepubertal girls. The etiology is unknown.
  • Contributing factors include local irritation, poor hygiene, and lack of estrogen, resulting in a mild inflammatory reaction.

Atrophy of the vulva

• Genital atrophy: Sometimes termed senile atrophy, genital atrophy is quite common in postmenopausal women and is a physiological condition related to aging and reduction of sexual hormones levels.

CLINICAL HISTORY AND PHYSICAL FINDINGS

Section 4 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

Nonneoplastic epithelial disorders

Inflammatory diseases

• Lichen sclerosus
• • This is commonly characterized by whitish lesions of the vulva. It is asymptomatic, but intractable pruritus can sometimes be present. Burning and pain are less likely manifestations. Clinically, the lesions are characterized by a wrinkled ("cigarette-paper") or parchmentlike (shiny, delicate, pale) appearance of the skin that commonly extends around the anal area in a figure-of-8 or keyhole configuration (see Image 1).
  • In late stages of the disease, normal architecture may be lost. Additionally, atrophy of the labia minora, constriction of the vaginal orifice (kraurosis), synechiae, ecchymoses, fissures, and telangiectases may be noted. Squamous cell carcinoma develops in 3-6% of women affected by vulvar lichen sclerosus, which is therefore now regarded as a preneoplastic condition. The presence and the duration of symptoms and the loss of vulvar architecture are not useful indicators of potential cancer risk.
• Squamous cell hyperplasia
• • Squamous cell hyperplasia appears as ill-defined, single or scattered, whitish, thickened, and sometimes verrucous plaques that may be accompanied by excoriations or fissurations that cause pain and soreness.
  • Itching is a common symptom. If hyperkeratosis is not prominent, lesions may appear as reddish plaques. The clitoris, labia minora, and inner aspects of the labia majora are more commonly affected.
  • Extensive lesions may result in stenosis of the vaginal introitus.
• Lichen simplex chronicus (localized neurodermatitis)
• • Patients with this condition present with a hyperkeratotic, usually ill-defined, grayish, thickened, and sometimes excoriated lesion, usually located over the labia majora and merging with normal skin.
  • Hyperpigmentation is common, and prominent skin markings are evident when the skin is involved. Itching is always present and may be intense.
• Primary irritant dermatitis
• • Typical physical findings include diffuse reddening of the involved skin with areas of excoriation. Secondary infection may occur.
  • An association with regional intertrigo, especially following mechanical irritation, may be observed (see Image 2).
  • Chronic irritant dermatitis may lead to squamous cell hyperplasia.
• Intertrigo
• • Typically, intertrigo is characterized by erythema, local edema, oozing, maceration, and fissuring of the inguinal fold, sometimes accompanied by considerable odor. It may be associated with similar findings in other skin folds.
  • The surrounding skin may show reactive postinflammatory hyperpigmentation. Soreness and itching are common symptoms. Secondary candidosis may exacerbate intertrigo.
• Allergic dermatitis
• • Physical examination often reveals dryness, scaling, excoriations, and, at times, ulceration (see Image 3). Itching is usually intense.
  • The clinical pattern may be subacute, with weeping and oozing, especially when bacterial superinfection occurs. Without treatment, allergic dermatitis can progress to squamous cell hyperplasia.
• Fixed drug eruption
• • This condition appears as an erythematous and edematous plaque that frequently involves the genital area and typically resolves, leaving postinflammatory hyperpigmentation.
  • The lesions are usually single at first presentation, but following reingestion of the drug, development of new elements may occur in addition to recurrence of the primary lesion.
  • The main complaint is burning, but some patients are asymptomatic or have mild pruritus.
• Atopic dermatitis
• • This condition consists of a subacute or chronic, symmetric, and ill-defined eczematous rash, usually involving the labia majora and, less frequently, the labia minora and inner thighs.
  • The eruption is characterized by mild erythema, dryness, and fine scaling. Itching and burning are common symptoms.
  • Excoriation secondary to repeated scratching may cause bacterial superinfection with honey-colored crusting and, in chronic forms, lichenification. In some patients, the itch-scratch-itch cycle may gradually lead to development of lichen simplex chronicus.
• Seborrheic dermatitis
• • When the vulva is involved, the labia majora and mons pubis are primarily affected.
  • The lesions appear as dry-to-greasy scales superimposed on red-to-yellow brownish plaques and are often pruritic, extending to the gluteal cleft and thighs (see Image 4).
• Psoriasis
• • Occasionally, psoriasis may manifest in infancy as a bright-red, glazed, and well-demarcated eruption in the napkin area (napkin psoriasis).
  • In adults, vulvar psoriasis usually involves the genitocrural areas and the lateral aspects of the labia majora, sparing the mucosa. It may range in severity from scattered, nonscaling erythematous patches (see Image 5) to thick, confluent erythematous plaques with silvery-white adherent scales covering all of the labia majora and the mons pubis.
  • Symptoms are highly variable and range from intense pruritus to minimal discomfort. Secondary changes, such as excoriations and lichenification or oozing and crusting from bacterial and yeast colonization, may occur.
• Reiter disease
• • In approximately half the affected patients, cutaneous lesions occur as psoriasiform, crusting, and sometimes pustular papules and plaques over the hands and feet. Circinate genital erosions or oral mucosa involvement are often associated. Conjunctivitis, arthritis, and low back pain may also occur.
  • The disease is unusual in women; therefore, vulvar lesions are poorly described. Red crusted plaques associated with vaginal discharge, circinate erosions, or linear ulcers associated with verrucous lesions and pustules have been observed.
• Lichen planus
• • In the vulvar area, the disease may occur in 3 patterns: papulosquamous, erosive, and hypertrophic.
  • • The papulosquamous form, occurring as part of a generalized disease, is the most common and is characterized by flat-topped, polyhedral, violaceous, shiny, and itchy papules located on keratinized skin of the labia and mons pubis. Delicate and whitish reticulated papules may be present on the mucosa, but no atrophy or scarring is observed.
    • The erosive form involves the mucous membranes of the mouth and vulvovaginal area and may be locally destructive, leading to atrophy and scarring. (Synonyms include erosive vaginal lichen planus, desquamative inflammatory vaginitis, vulvovaginal-gingival syndrome, and ulcerative lichen planus.) Itching is rare, but pain, burning, and irritation occur and may be responsible for dyspareunia and dysuria.
    • The rare hypertrophic form, clinically resembling lichen sclerosus, manifests with extensive white scarring of the periclitoral area with variable degrees of hyperkeratosis. It may be very itchy. Extensive vaginal involvement may result in a malodorous discharge. Large denuded areas may become adherent, causing stenosis of the vaginal introitus and dyspareunia. Marked atrophy may develop with time.
  • Malignancy is possible in long-standing and ulcerative lichen planus.
• Lupus erythematosus
• • Vulvar manifestations may be different in each clinical subset of the disease. In chronic discoid lupus erythematosus, the skin is mostly involved (rarely, the mucous membranes). Vulvar involvement may occur as a scarred plaque of variable size with or without central ulceration and with marked peripheral hyperpigmentation located anywhere on the vulva or perineum.
  • In subacute and systemic lupus erythematosus, the patient is usually asymptomatic and a lichen planus–type reticulated pattern may sometimes be observed. Occasionally, tender, punched-out mucosal ulcers with possible scarring occur in the vestibule or vagina.
• Darier disease
• • Onset is usually in late childhood, with keratotic, crusted, skin-colored, yellow, or brown papules located mainly on the neck, upper thorax, and flexural areas. These papules grow and multiply and tend to become more widespread and verrucous with age.
  • The vulva is often involved. As the condition becomes more pronounced, hygiene becomes progressively difficult to maintain, and the buildup of keratotic debris causes secondary infection and a foul smell.
• Aphthosis
• • Patients report single or multiple, sharply demarcated, punched-out, and shallow vulvar ulcers with fibrinous bases and erythematous borders. The lesions are very painful and are sometimes accompanied by systemic symptoms, such as fever and malaise, but they are usually self-limited, clearing spontaneously in a few weeks.
  • In some cases, especially in older women, relapsing episodes akin to partial Behçet disease may occur. In time, older patients with recurrent ulcers may develop Behçet disease or inflammatory bowel disease.
• Behçet disease
• • This disease is a rare multisystem disorder characterized by the triad of oral ulcers, genital ulcers, and posterior uveitis; however, almost any organ system may be involved.
  • Oral ulcers are usually multiple and recurrent and may sometimes be extensive, showing a pseudomembranous coating.
  • Vulvar ulcers, ranging in diameter from a few millimeters to 3 cm, often appear as multiple crops of well-defined and very tender ulcers with fibrinous bases and considerable undermining.
  • Fistulae, with partial or complete destruction of the labia, may develop.
  • Other manifestations of the disease include fever, malaise, acneiform lesions or cutaneous nodules on the skin, arthritis, synovitis, and thrombophlebitis. Associated erythema nodosum and erythema multiforme have been reported.
• Pyoderma gangrenosum
• • This condition often appears as a deep, painful nodule or pustule that breaks down, draining a purulent discharge and forming an irregular ulcer with distinct undermined and purplish edges. The lesion extends peripherally as the inflammatory process spreads within the dermis.
  • Satellite pustules may be observed, eventually coalescing and forming a multicentric ulceration.
  • Pain is intense, and the course of the disease is unpredictable. The lesion may heal spontaneously, remain quiescent for months (even years), or worsen again after minimal trauma, surgery, or an inapparent triggering cause.
• Crohn disease
• • Cutaneous changes may occur before the onset of bowel symptoms. The area of involvement may extend to the perineal and perianal area. Localized or generalized labial edema, with erosions and multiple painful ulcers of variable severity, may be observed. Ulcers may be solitary, deep, and necrotic, possibly leading to formation of fistulae.
  • Unilateral labial hypertrophy, coalescing pustules, and vegetating lesions mimicking anogenital warts (pyostomatitis vegetans) have also been described.
• Hidradenitis suppurativa
• • In the vulvar area, this disease primarily affects the labia majora and intercrural folds, with erythematous acneiform papules, nodules, and cysts scattered among multiheaded comedones, but it may also involve the mons pubis, labia minora, and clitoris.
  • In some cases, deep, painful subcutaneous nodules may ulcerate and ooze a purulent yellow discharge, leading to open sinuses and extensive scarring; in other cases, nodules may coalesce, thus forming conglobate plaques interconnected by sinus tracts. Over time, pseudoepitheliomatous hyperplasia may develop. Occasionally, vulval squamous cell carcinoma has been observed arising in chronic hidradenitis suppurativa.
• Fox-Fordyce disease: This itchy papular eruption of the axillary and anogenital regions appears on the vulva as multiple, monomorphous, skin-colored or slightly hyperpigmented, dome-shaped follicular lesions, mainly involving the mons pubis and labia majora.
• Plasma cell vulvitis: This condition appears as an erythematous, well-demarcated, smooth, and shiny plaque that may be either asymptomatic or cause mild itching, burning, or soreness.
• Vulvar vestibulitis
• • This condition is characterized by severe burning and pain with vestibular touch or attempted vaginal entry. Typically, it follows a chronic course and may show variable numbers of minute spots of vestibular erythema, ranging in diameter from 2-7 mm. Rarely, small ulcerations are detectable.
  • The pain is enough to make intercourse uncomfortable or completely impossible. Associated deep pain from secondary vaginismus may occur. Understandably, varying degrees of sexual dysfunction may cause depression and anxiety.

Blistering diseases

• Familial benign chronic pemphigus (Hailey-Hailey disease)
• • Hailey-Hailey disease is characterized by recurrent eruptions of vesicles and blisters that easily erode and develop crusting. Painful deep fissures may also occur. The lesions typically involve the inguinal fold and may extend along the edge of the labia majora and on the inner aspect of the thighs (see Image 6).
  • Bacterial and fungal superinfections often occur.
• Bullous pemphigoid
• • The course of this disease is chronic and benign. Often, a prodromal phase of fixed urticarial plaques occurs with itching and irritation, which can be generalized.
  • On the vulva, blisters arising on the labia easily erode, leaving erosions that may cause variable degrees of discomfort.
• Cicatricial pemphigoid
• • In this disorder, blisters typically develop on mucosal sites, gradually leading to the development of disabling scarring adhesions.
  • Common symptoms include vulvar itching, soreness, and pain, along with the presence of mucosal erosions and vaginal discharge. Vulvar involvement may cause synechiae of the labia and/or vagina, with consequent dyspareunia.
• Pemphigus vulgaris
• • Erosions, either arising on the mucosa of the inner labia and vestibule (see Image 7) or on vulvar skin (see Image 8), cause considerable burning and pain.
  • Long-term disease may result in vulvar scarring, vaginal scarring, or both.
• Erythema multiforme (minor/major)
• • Vesicular and bullous lesions with a typical iris pattern may show variable symmetrical extension according to the severity of the disease.
  • In the major form, blistering of the mucous membranes is extensive and may cause the formation of synechiae in later stages of the disease (see Image 9).
• Epidermolysis bullosa: Genital involvement has been reported in dystrophic forms of the disease and may cause painful blistering in the vulvar area with consequent scarring, vaginal obstruction, and obstructive uropathy.

Pigmentary changes

• Acanthosis nigricans
• • The skin of the inguinal and axillary regions appears diffusely hyperpigmented with a velvety or warty surface.
  • Patients with this condition are usually asymptomatic, but some report local irritation and pruritus.
  • The malignant form is associated with a malignant tumor, most commonly a gastric carcinoma, a lymphoma, or a sarcoma.
• Lentigo, lentiginosis, and benign vulvar melanosis
• • Lentigo appears as a small (<4 mm), hyperpigmented, brownish macule that may be found anywhere on the vulvar skin or mucosa.
  • Lentiginosis is characterized by a circumscribed grouping of pigmented small macules with normal background pigmentation.
  • In vulvar melanosis, larger brown-to-black macules (£10 cm in diameter), often showing irregular margins, are observed (see Image 10).
• Melanocytic nevus
• • Melanocytic nevi appear as small, circumscribed, variably pigmented macules or raised papules that may be congenital or acquired.
  • Some authors have suggested that nevi occurring on the vulva are more likely to undergo malignant transformation; therefore, careful examination is recommended.
• Postinflammatory hyperpigmentation
• • Varying degrees of macular or patchy hyperpigmentation may occur.
  • The color can range from brown to black, although it is usually irregular and can also show scattered patches of hypopigmentation.
• Postinflammatory hypopigmentation: This condition is characterized by diffuse depigmentation or patches of hypomelanosis that may be single or multiple and variably involve vulvar skin.
• Vitiligo: Patients with vitiligo may develop asymptomatic progressively enlarging white patches on the vulvar skin and mucosae that, in fair-skinned individuals, may be barely appreciable upon clinical observation using a natural light source.

Benign tumors, hamartomas, and cysts

• Mucous cysts
• • These cysts usually cause no symptoms and appear as a lump or mass that may be found at the introitus and labia minora.
  • Cysts of the canal of Nuck can give rise to a hydrocele located high in the labia majora and are associated with a concurrent inguinal hernia in 30% of cases.
• Bartholin cyst and Skene duct cyst
• • Bartholin cysts are the most common vulvar cystic growths. They usually occur in the lower and lateral portion of the labia majora, although lesions expanding anteriorly have also been described, and, if large, they may cause variable discomfort, hampering sexual intercourse and micturition.
  • Skene duct cysts arise adjacent to the urethral meatus and, if large enough, may cause urinary obstruction.
  • In both conditions, acute infection with abscess formation may occur, thus causing considerable pain.
• Epidermal inclusion cyst
• • These cysts are most commonly observed in the vagina, but they can also be found on the vulva (see Image 11).
  • Such cysts are subcutaneous and generally asymptomatic unless they become infected. Spontaneous rupture often occurs.
• Seborrheic keratosis
• • Seborrheic keratoses appear as single or multiple verrucous, roundish, yellowish-brown, sharply circumscribed papules ranging in diameter from 2-10 mm and covered with a greasy friable scale.
  • They often have a "stuck-on" appearance.
• Acrochordon: These lesions, often multiple and appearing as soft, pedunculated, brown, tan, or skin-colored lesions (0.2-1.5 cm in diameter), can particularly be found in the inguinal folds of obese and/or diabetic patients.
• Fibroma, fibromyoma, and dermatofibroma
• • Fibromas, fibromyomas, and dermatofibromas usually appear as solitary, slightly raised, gray-brown, mobile indurated lesions (3-8 mm in diameter) developing along the insertion of the round ligament into the labia majora.
  • Fibromas may be pedunculated and may rarely reach a considerable size.
  • In dermatofibromas, lateral compression produces a slight indentation known as the dimple sign, which is characteristic of these tumors. These lesions usually cause no symptoms until they reach a larger size and/or are located near the introitus or urethra.
• Lipoma
• • On the labia majora, lipomas may appear as soft sessile or pedunculated masses varying in diameter from 1 cm to several centimeters.
  • Large lesions may gradually ulcerate.
• Hidradenoma
• • Hidradenomas usually occur in postpuberty as single mobile nodules (~1-1.5 cm in diameter) arising in the interlabial sulcus.
  • Ulceration may occur, and in these cases, the lesions may show an exophytic proliferation clinically resembling a malignant neoplasm.
• Hemangioma
• • Most genital hemangiomas involve the labia majora, but the labia minora, the perineal area, and the perianal area may also be involved to varying degrees. They appear as red macules that rapidly progress to well-circumscribed, raised, red, and soft lesions of variable size (see Image 12).
  • Over time, regression occurs, with involution and fibrosis. Possible complications include ulceration, bleeding, urethral obstruction, and Kasabach-Merritt syndrome (a consumptive coagulopathy mainly described in association with large hemangiomas).
• Lymphangioma: This condition is usually detected early in infancy on the labia minora or majora as an asymptomatic, raised, compressible, doughy mass, sometimes showing multiple clustered, superficial, thin-walled, translucent, and persistent pseudovesicles filled with clear fluid that may progressively grow over time.
• Angiokeratoma
• • Angiokeratomas manifest as 1-3 mm, dark, red-to-purple, and sometimes hyperkeratotic papules (see Image 13). Patients are usually asymptomatic.
  • Occasionally, patients become symptomatic, with vulvar itch, discomfort, or pain. The lesions may bleed as a result of trauma. When they appear in teenagers and are associated with angiokeratomas of the lower abdomen, Fabry disease should be excluded.
• Pyogenic granuloma
• • Pyogenic granuloma appears as a bright red papule or nodule of no more than 1-2 cm in diameter; erosion and bleeding may occur.
  • It may persist indefinitely unless destroyed.
• Endometriosis
• • Often painful, vulvar endometriosis manifests as an ill-defined, dark red, brown, or blue-black cystic papule or nodule, usually located on the posterior fourchette. A case of endometriosis infiltrating the Bartholin gland has been observed.
  • It sometimes shows a cyclical variation in size and symptoms according to menses. More widespread involvement is a significant cause of pain and distress.
• Heterotopic sebaceous glands and sebaceous gland hyperplasia
• • Heterotopic sebaceous glands often arise on the labia minora and inner aspects of the labia majora as multiple superficial yellow papules (1-3 mm in diameter) that can be clearly seen when the mucosa is stretched.
  • The clinical features of sebaceous gland hyperplasia differ from those of typical lesions on the face and have been described as polypoid tumors no greater than 2.5 cm in diameter on the labia majora, covered by normal-appearing skin. These lesions may regress, and they have no malignant potential.
• Papillomatosis (papillary vulvar hirsutism)
• • These lesions are found distal to the hymenal ring (see Image 14).
  • They consist of raised, fleshy, skin-colored, soft, asymptomatic micropapillae of the inner labia minora, usually 1-3 mm in diameter and symmetric, that occur singly or become confluent, forming a fimbriated fringe.

Congenital malformations

• Ambiguous external genitalia
• • Infants with female pseudohermaphroditism usually present with an enlarged phallus, alone or associated with some degree of labioscrotal fusion.
  • Reduced levels of cortisol and consequent sodium depletion, which can be life threatening in neonates, may be associated in forms resulting from 21-hydroxylase deficiency.
  • Underdevelopment of male genitalia can yield a female phenotype in the most extreme cases of male pseudohermaphroditism.
• Congenital labial hypertrophy
• • The patient is asymptomatic except for nuisances regarding hygiene, physical activity, or sexual intercourse. The large labia may be unilateral or bilateral (see Image 15).
  • If hygienic care is not maintained, erythema and irritation may result.
• Labial adhesions: The extent of fusion varies and often causes no symptoms. The natural history is one of spontaneous resolution with pubertal estrogenization.

Atrophy of the vulva

• The mucosal surface is dry, and mild atrophy of the labia minora, clitoris, and inner aspects of the labia majora occurs.
• The clinical appearance may resemble that of the later stages of lichen sclerosus. These patients have relatively few symptoms, and hyperkeratosis is not evident.

HISTOLOGIC FINDINGS

Section 5 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

Nonneoplastic epithelial disorders

Inflammatory diseases

• Lichen sclerosus: Histologic findings include hyperkeratosis, epithelial thinning with flattening of the rete pegs, cytoplasmic vacuolation of basal keratinocytes, follicular plugging, homogenization of the subepithelial layer, and inflammatory cell infiltration consisting of lymphocytes with few plasma cells.
• Squamous cell hyperplasia
• • Histologic examination reveals thickening of the keratin layer (hyperkeratosis) greater than that seen with lichen sclerosus and lengthening and distortion (acanthosis) of the rete pegs.
  • Cellular elements of the epithelium proliferate, but maturation is usually normal. An inflammatory response in the dermis usually occurs, consisting of lymphocytic and plasma cell infiltration. Varying degrees of cellular atypia with increased mitotic activity and loss of polarity may be observed in the epidermis.
  • This vulval squamous epithelial hyperplasia with atypia corresponds to the entity formerly indicated as leukoplakia, which has a malignant potential. It appears to be related to conditions that approximate vulvar intraepithelial neoplasms (VINs) and has been found to progress to invasive carcinoma in 10% of cases.
• Lichen simplex chronicus (localized neurodermatitis)
• • Histologically, epidermal and epithelial hyperplasia, hyperkeratosis, and fibrotic vertical streaks of collagen between the hyperplastic rete are present.
  • A superficial perivenular infiltrate is also present.
• Primary irritant dermatitis
• • Histologic features are highly variable, from extensive ulceration to diffuse parakeratosis with vascular congestion and ectasia to a spongiotic pattern essentially identical to allergic contact dermatitis.
  • In some instances, a significant individual keratinocyte necrosis with nuclear karyorrhexis and cytoplasmic pallor occurs.
• Intertrigo: Histopathologic findings are nonspecific.
• Allergic dermatitis
• • In the epidermis, variable degrees of intercellular edema and spongiosis are present, which may eventually lead to the development of an intraepidermal vesicle. Lymphocytic infiltration of the epidermis is always present.
  • Concomitant with these changes are varying degrees of epithelial proliferation ranging from mild acanthosis in early acute dermatitis to a psoriasiform epidermal hyperplasia in chronic variants. The dermis is often congested, and edema is usually marked in active lesions.
• Fixed drug eruption
• • Histologic changes resemble those of erythema multiforme. Necrosis of keratinocytes in the stratum malpighii occurs.
  • Scattered dyskeratotic keratinocytes with eosinophilic cytoplasm and pyknotic nuclei are frequently seen in the epidermis and represent apoptosis.
• Atopic dermatitis
• • Mild spongiosis, exocytosis of lymphocytes, and parakeratosis are present in the epidermis. Hyperkeratosis and wedge-shaped hypergranulosis may also be observed.
  • A perivascular lymphocytic infiltrate with scattered histiocytes is present in the superficial dermis.
• Seborrheic dermatitis
• • The histopathologic features are a combination of those observed in psoriasis and spongiotic dermatitis.
  • Moderate acanthosis with focal areas of parakeratosis, regular elongation of the rete ridges, mild spongiosis, and focal exocytosis of lymphocytes are noted. The dermis contains a sparse mononuclear cell infiltrate.
• Psoriasis: The histologic picture varies considerably with the stage of the lesion and is usually diagnostic only in early scaling papules and near the margin of advancing plaques, ie, acanthosis with regular elongation of the rete ridges, thinning of suprapapillary epidermis with occasional small spongiform pustules, diminished or absent granular layer, confluent parakeratosis, elongation and edema of the dermal papillae, and dilated and tortuous capillaries.
• Reiter disease
• • Early pustular lesions show a spongiform macropustule in the upper epidermis that is indistinguishable from the spongiform pattern observed in pustular psoriasis.
  • Parakeratosis and elongation of the rete ridges are also noted.
• Lichen planus: Vulvar lichen planus shows a dense dermal inflammatory infiltrate extending to the dermoepidermal junction in conjunction with a prominent granular cell layer, hyperkeratosis, and acanthosis.
• Lupus erythematosus
• • Histologic findings alone may not be sufficient to allow correct classification of the subtype of eruption.
  • In well-developed lesions, hydropic degeneration of the basal cell layer occurs in association with edema of the upper dermis and extravasation of erythrocytes.
  • Fibrinoid deposits in the connective tissue of the skin are not specific but are often observed in erythematous, edematous lesions, especially in patients with systemic lupus erythematosus.
  • Subcutaneous fat is often involved in systemic disease.
• Darier disease
• • The typical histological hallmarks of Darier disease are hyperkeratosis, with a peculiar form of dyskeratosis resulting in the formation of corps ronds and grains and suprabasal acantholysis, leading to the formation of suprabasal clefts or lacunae with irregular upward proliferation of papillae lined with a single layer of basal cells.
  • A chronic inflammatory infiltrate is present in the dermis.
• Aphthosis: Histological features include necrotizing vasculitis of the superficial postcapillary venules with associated fibrinoid necrosis, endothelial swelling, and lymphocytic perivascular infiltrate with sometimes abundant neutrophils.
• Behçet disease: Vulvar lesions show features similar to those of minor aphthosis.
• Pyoderma gangrenosum
• • Although suggestive, histopathologic features alone are not diagnostic.
  • Features include dermal edema; dense, diffuse neutrophilic infiltrate; engorgement and thrombosis of small-to-medium–sized vessels; necrosis; and hemorrhage.
• Crohn disease
• • Discrete noncaseating granulomas with isolated multinucleated giant cells are present throughout the superficial and deep dermis, with extension into subcutaneous tissue.
  • Occasionally, the granulomatous infiltrate is perivascular and may create secondary vascular changes.
• Hidradenitis suppurativa: Histology shows chronic dermal inflammation with fibrosis and foreign body giant cells and the presence of neutrophils and bacteria in apocrine gland ducts.
• Fox-Fordyce disease: Histologic examination shows enlarged apocrine sweat glands surrounded by a dermal inflammatory infiltrate.
• Plasma cell vulvitis: Below an atrophic epidermis showing no signs of keratinocyte atypia, a dense lichenoid infiltrate with a large number of plasma cells and occasional dilated blood vessels and hemosiderin deposition is evident in the upper and mid dermis.
• Vulvar vestibulitis
• • Histologic examination reveals a nonspecific, chronic lymphocytic inflammatory infiltrate in the dermis, with foci of squamous metaplasia of the minor vestibular glands that may show nodular hyperplasia in some cases.
  • Some patients are found to have koilocytosis after biopsy and/or human papillomavirus infection after in situ hybridization testing.

Blistering diseases

• Familial benign chronic pemphigus (Hailey-Hailey disease): Epidermal parakeratosis and dyskeratotic suprabasal acantholysis, with the typical appearance of a dilapidated brick wall, are common findings.
• Bullous pemphigoid: A typical histopathological finding on direct immunofluorescence is the presence of a subepidermal blister with deposition of immunoglobulins along the basement membrane.
• Cicatricial pemphigoid
• • In addition to subepidermal splitting, lamellar fibrosis beneath the epidermis is a hallmark of this condition, but it may not be present in the initial lesions.
  • Neutrophils and lymphocytes predominate in the inflammatory infiltrate.
• Pemphigus vulgaris
• • Rarely, the earliest recognized change may be eosinophilic spongiosis; more commonly, the earliest noted change is spongiosis in the lower epidermis.
  • Acantholysis first leads to the formation of clefts and then to blisters in a predominantly suprabasal location.
• Erythema multiforme (minor/major)
• • Erythema multiforme is considered the prototype of the vacuolar form of interface dermatitis. Because of its acute nature, an orthokeratotic stratum corneum is formed.
  • Mild spongiosis and exocytosis are observed. Necrosis of keratinocytes in the stratum malpighii is typical.
• Epidermolysis bullosa
• • Dermoepidermal fissuring is a common feature.
  • Different histopathologic, ultrastructural, and laboratory findings may be observed according to the clinical subset of disease.

Pigmentary changes

• Acanthosis nigricans: Histologic examination reveals hyperkeratosis and papillomatosis but only slight, irregular acanthosis and, usually, no hyperpigmentation.
• Lentigo, lentiginosis, and benign vulvar melanosis: A slight or moderate elongation of the rete ridges with an increase in the concentration of melanocytes in the basal layer is observed.
• Melanocytic nevus
• • Typical findings are nests of round melanocytic cells without dendrites and no sign of atypia.
  • Histopathology allows identification of all the evolutional steps of these lesions, which typically begin as junctional nevi and, after having become intradermal nevi, undergo involution.
• Postinflammatory hyperpigmentation
• • Epidermal melanin is increased.
  • Melanophages are present in the superficial dermis, along with a variably dense lymphohistiocytic infiltrate around superficial blood vessels and in dermal papillae.
• Postinflammatory hypopigmentation
• • Epidermal melanin is decreased.
  • A superficial and perivascular lymphohistiocytic infiltrate may be observed in the dermis.
• Vitiligo: The central process is the destruction of melanocytes at the dermoepidermal junction.

Benign tumors, hamartomas, and cysts

• Mucous cysts: Histologically, mucous cysts show a fibrous wall lined by epithelial cubical cells and filled with mucin or, in the case of canal of Nuck cysts, a clear fluid.
• Bartholin cysts and Skene duct cysts: These cysts show a fibrous wall lined by a flattened epithelium.
• Epidermal inclusion cysts: Epidermal cysts have a wall composed of true epidermis and are filled with horny material arranged in laminated layers.
• Seborrheic keratosis: This is an exophytic and papillomatous proliferation of basaloid epidermal cells containing horn cysts and often showing marked basal and suprabasal intracellular melanin pigmentation.
• Acrochordon: Loose connective tissue rich in vessels covered by normal epidermis is observed.
• Fibroma, fibromyoma, and dermatofibroma
• • Fibroma, fibromyoma, and dermatofibroma show a well-demarcated area of interwoven collagen fiber bundles without elastic fibers covered by normal or hyperplastic epidermis.
  • In fibromyoma, muscle fiber bundles are evident. A dermatofibroma is a variant of the fibromyoma group that, because of its vascularity, can present a confusing histologic picture.
• Lipoma: By definition, the principal component of lipomas is mature adipocytes.
• Hidradenoma: Histopathologic features may be confusing; for example, a complex papillary-adenomatous pattern arranged in an aggressive fashion with absent mitoses may be observed.
• Hemangioma
• • Early lesions are very cellular with few vascular channels; mitotic figures and mast cells may be prominent.
  • Later, vessel lumina become apparent, producing a cavernous pattern.
• Lymphangioma: Cavernous dilated lymphatic channels of different sizes are evident in the dermis or subcutaneous fat and sometimes extend into the overlying epidermis.
• Angiokeratoma: Histopathologic features consist of hyperkeratosis and epidermal acanthosis overlying a dermis that contains dilated capillary vessels in proximity to the epidermis.
• Pyogenic granuloma: This is a lobular vascular proliferation with distinctive plump epithelioid endothelial cells admixed with a varying lymphocytic and eosinophilic infiltrate that tends to obscure the vessels.
• Endometriosis: Typical glandular and stromal tissue of the endometrium lying within the dermis are observed.
• Heterotopic sebaceous glands and sebaceous gland hyperplasia: Histologic examination shows sebaceous gland hyperplasia.
• Papillomatosis (papillary vulvar hirsutism): Histologically, these lesions are angiofibromas.

Congenital malformations

• Ambiguous external genitalia, congenital labial hypertrophy, and labial adhesions: No definitive histologic changes occur.

Atrophy of the vulva

• No definitive histologic changes occur.

DIFFERENTIAL DIAGNOSIS AND WORKUP

Section 6 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

Nonneoplastic epithelial disorders

Inflammatory diseases

• Lichen sclerosus
• • The differential diagnosis includes lichen planus, vitiligo, postmenopausal atrophy, cicatricial pemphigoid, extramammary Paget disease, and sexual abuse.
  • A skin biopsy is necessary to confirm the diagnosis and to exclude the presence of malignant degeneration.
• Squamous cell hyperplasia
• • The diagnosis is one of exclusion after psoriasis, lichen sclerosus, lichen planus, and chronic eczematous dermatitis have been ruled out.
  • In doubtful cases, a biopsy is suggested. This also helps identify cases of squamous cell hyperplasia with atypia that may have a propensity to develop carcinoma.
• Lichen simplex chronicus (localized neurodermatitis): Primary irritant dermatitis, chronic eczematous dermatitis, squamous cell hyperplasia with or without atypia, and lichen planus should be excluded.
• Primary irritant dermatitis
• • The differential diagnosis includes candidal vulvitis and allergic contact dermatitis.
  • Skin swabs and patch testing are useful to exclude superimposed bacterial or fungal infections and allergic contact dermatitis, respectively.
• Intertrigo
• • The clinical presentation is often diagnostic. The differential diagnosis includes candidosis and other conditions that may be found in intertriginous areas, such as familial benign chronic pemphigus (Hailey-Hailey disease), psoriasis, and seborrheic dermatitis.
  • Bacterial and mycological investigations may be useful to detect secondary infections.
  • Skin biopsy is indicated when treatment fails or when an underlying disorder (eg, Hailey-Hailey disease) is considered possible.
• Allergic dermatitis
• • The differential diagnosis includes atopic dermatitis psoriasis, intertrigo, and tinea.
  • The diagnosis is usually made on the basis of history findings, although less obvious cases may require patch tests. Because vulvar epithelium is more permeable than exposed skin, standard clinical patch tests may not sufficiently mimic vulvar exposures.
• Fixed drug eruption
• • The differential diagnosis includes recurrent herpes simplex virus (HSV) infection, lichen planus, intertrigo, and bullous pemphigoid.
  • Clinical history and typical morphological features usually confirm the diagnosis.
• Atopic dermatitis
• • The differential diagnosis includes psoriasis, seborrheic dermatitis, contact dermatitis, and eczematous candidiasis.
  • The diagnosis is made based on personal and family history and on clinical detection of typical lesions elsewhere in the body. Histology is seldom necessary.
• Seborrheic dermatitis
• • The differential diagnosis includes tinea, psoriasis, and other scaling disorders, and it may sometimes be clinically difficult to confirm.
  • The presence of characteristic lesions elsewhere on the body may indicate the diagnosis.
• Psoriasis
• • The differential diagnosis includes seborrheic dermatitis, candidal or dermatophyte infection, lichen simplex chronicus, and contact dermatitis.
  • Biopsy is confirmatory but is seldom needed because the diagnosis is often clinical.
• Reiter disease
• • The diagnostic dilemma is differentiating Reiter syndrome from pustular psoriasis. Acrodermatitis enteropathica and lymphogranuloma venereum should also be considered in the differential diagnosis.
  • Discrimination points include cervicitis, which is common in Reiter syndrome but not reported in psoriasis; the greater prevalence of HLA-B27 positivity; iritis; conjunctivitis; and other mucous membrane lesions in Reiter syndrome.
  • Biopsy, radiographs, and laboratory investigations are usually necessary to confirm the diagnosis and to assess the extent and severity of the disease.
• Lichen planus
• • The differential diagnosis includes psoriasis, dermatophyte infection, lichen simplex chronicus, lichen sclerosus, cicatricial pemphigoid, pemphigus, lupus erythematous, and bullous pemphigoid.
  • Although demonstration of typical oral changes carries more diagnostic weight than biopsy, histopathology is often necessary to confirm the diagnosis.
• Lupus erythematosus
• • The differential diagnosis includes all causes of genital ulcers and lichen planus in its clinical variants.
  • Clinical presentation, histopathology, and immunohistopathology define the diagnosis. To confirm the diagnosis, histopathologic, immunohistopathologic, and serologic investigations are required. The latter include indirect immunofluorescence for antinuclear antibodies.
• Darier disease
• • The differential diagnosis of lesions located in the genital and perineal area includes acanthosis nigricans, benign familial pemphigus, and impetigo.
  • Clinical diagnosis necessitates histopathologic confirmation.
• Aphthosis
• • The diagnosis is essentially clinical and one of exclusion, following appropriate cultures, serologic testing, and biopsies to rule out other conditions. Histological features alone are not diagnostic.
  • The differential diagnosis includes HSV infection, chancroid, granuloma inguinale, tuberculosis, syphilis, lymphogranuloma venereum, and Crohn disease.
• Behçet disease
• • The differential diagnosis for vulvar lesions is the same as that for aphthosis.
  • Diagnosis of systemic disease is based on a history of recurrent oral ulcers in conjunction with genital ulcers, eye findings, or skin lesions.
• Pyoderma gangrenosum: Bacterial and mycobacterial infections, tropical ulcers, tertiary syphilis, chronic ulcerative HSV infection, deep mycoses, ecthyma gangrenosum, and postoperative progressive gangrene are excluded based on history findings, clinical features, and laboratory investigations.
• Crohn disease
• • The differential diagnosis includes hidradenitis suppurativa, Behçet disease, lymphogranuloma venereum, cutaneous sarcoidosis, and genitourinary tuberculosis.
  • Biopsy findings show the typical granulomatous changes.
• Hidradenitis suppurativa
• • The differential diagnosis includes bacterial infections, Crohn disease, and lymphogranuloma venereum.
  • The diagnosis is usually made based on clinical findings rather than histological findings.
• Fox-Fordyce disease
• • The differential diagnosis includes syringomata and folliculopapular lichen simplex chronicus.
  • The clinical presentation and biopsy findings define the diagnosis.
• Plasma cell vulvitis
• • Clinically, plasma cell vulvitis may mimic low-grade VINs and in situ carcinomas involving the same mucosal area.
  • Histopathological examination is necessary to exclude intraepithelial carcinoma and to confirm the diagnosis.
• Vulvar vestibulitis
• • The differential diagnosis includes cyclic monilial vulvovaginitis and dysesthetic vulvodynia.
  • The diagnosis is based on the history, the physical findings, and the lack of another satisfactory etiology. Biopsy is not diagnostic.

Blistering diseases

• Familial benign chronic pemphigus (Hailey-Hailey disease)
• • The differential diagnosis includes intertrigo, other autoimmune blistering disorders, HSV infection, and psoriasis.
  • Diagnosis is easily confirmed on the basis of clinical features, family history, and histopathological findings.
• Bullous pemphigoid
• • The differential diagnosis includes pemphigus vulgaris, bullous drug eruptions, cicatricial pemphigoid, and erythema multiforme.
  • Direct immunofluorescence is necessary to confirm the diagnosis. Circulating antibasement membrane antibodies can be found in the sera of 70% of patients and may be identified by immunoblotting techniques.
• Cicatricial pemphigoid
• • The differential diagnosis includes erosive lichen planus and lichen sclerosus.
  • A biopsy for routine and immunofluorescent histopathology, showing linear deposits of immunoglobulins along the basement membrane, is usually confirmatory. Immunoblotting shows the presence of circulating autoantibodies in 30-50% of cases.
• Pemphigus vulgaris
• • The differential diagnosis includes bullous and cicatricial pemphigoid, erosive lichen planus, erythema multiforme, fixed drug eruption, and paraneoplastic pemphigus.
  • Diagnosis is made on the basis of clinical presentation and is confirmed by histology and immunofluorescence test results.
• Erythema multiforme (minor/major)
• • The differential diagnosis includes pemphigus vulgaris, bullous pemphigoid, drug reaction, and toxic epidermal necrolysis.
  • Diagnosis is made based on the clinical pattern and is confirmed by histological examination.
• Epidermolysis bullosa
• • Familial and clinical histories are useful to suggest the diagnosis.
  • Ultrastructural and immunohistochemical evaluation and genetic investigations (DNA mutation analysis) are required for final confirmation and identification of the disorder.

Pigmentary changes

• Acanthosis nigricans
• • The malignant type differs from the benign types by showing more extensive and more pronounced lesions.
  • Endocrinological investigations are recommended.
• Lentigo, lentiginosis, and benign vulvar melanosis
• • The differential diagnosis of lentigo and vulvar melanosis includes postinflammatory hyperpigmentation, melanocytic nevi, malignant melanoma, and pigmented basal cell carcinoma.
  • The role of dermoscopy in the diagnosis of pigmented mucosal lesions is currently still under evaluation. Histopathological examination may be necessary to confirm the diagnosis.
  • In cases of lentiginosis, rule out Peutz-Jeghers syndrome, LEOPARD syndrome, and inguinal freckling associated with neurofibromatosis.
• Melanocytic nevus
• • The differential diagnosis includes lentigo, melanoma, seborrheic keratosis, and pigmented basal cell carcinoma.
  • Diagnosis is confirmed by histopathology findings.
• Postinflammatory hyperpigmentation
• • The differential diagnosis includes benign vulvar melanosis and vulvar intraepithelial neoplasia.
  • The clinical picture and confirmatory skin biopsy define the diagnosis.
• Postinflammatory hypopigmentation: The differential diagnosis includes vitiligo and lichen sclerosus.
• Vitiligo
• • The differential diagnosis includes postinflammatory hypopigmentation, piebaldism, and lichen sclerosus. The diagnosis is clinical.
  • Wood lamp examination may allow a better assessment of the extent of disease in fair-skinned individuals. Histopathology is often unnecessary.

Benign tumors, hamartomas, and cysts

• Mucous cyst, Bartholin cyst, Skene duct cyst, and epidermal inclusion cyst
• • Differential diagnosis includes cystic and solid lesions of the vulva, such as hidradenoma papilliferum, lipoma, fibroma, endometriosis.
  • Diagnosis is usually clinical. In case of nonspecific clinical findings, excisional biopsy is recommended.
• Seborrheic keratosis
• • The differential diagnosis includes bowenoid papulosis, melanocytic nevus, melanoma, pigmented basal cell carcinoma, and verruciform xanthoma.
  • Dermoscopy may be helpful to rule out other pigmented vulvar lesions.
• Acrochordon
• • Diagnosis is clinical.
  • The differential diagnosis includes melanocytic nevus, neurofibroma, molluscum, and neuroma.
• Fibroma, fibromyoma, and dermatofibroma
• • Diagnosis is usually clinical.
  • The differential diagnosis includes dermal melanocytic nevus, histiocytoma, leiomyoma, neurofibroma, and keloid.
• Lipoma: Diagnosis is clinical and confirmed by biopsy.
• Hidradenoma
• • Diagnosis requires histopathological examination.
  • If ulceration is present, malignant adenocarcinoma must be excluded.
• Hemangioma
• • Diagnosis is clinical.
  • Biopsy samples are seldom taken from hemangiomas.
• Lymphangioma: Diagnosis is usually clinical. The lesion may sometimes be clinically misdiagnosed as anogenital warts, molluscum contagiosum, or other noninfectious conditions, and in such cases diagnosis is made by biopsy.
• Angiokeratoma
• • The differential diagnosis includes melanoma, vulvar warts, and nevi.
  • The diagnosis is based on clinical and histopathologic features.
• Pyogenic granuloma: This growth may closely resemble a nodular melanoma, but the short history, the pedunculated growth, and the epithelial collar are typical.
• Endometriosis
• • These lesions may be clinically suggestive of a melanoma.
  • Typical histology is confirmatory.
• Papillomatosis (papillary vulvar hirsutism)
• • The differential diagnosis includes human papillomavirus infection.
  • Diagnosis is made based on clinical findings showing monomorphous papules with a symmetric distribution.
• Heterotopic sebaceous glands and sebaceous gland hyperplasia
• • The diagnosis of heterotopic sebaceous glands is clinical, and no biopsy is needed.
  • The diagnosis of a solitary raised tumor usually requires histological confirmation.

Congenital malformations

• Ambiguous external genitalia, congenital labial hypertrophy, and labial adhesions
• • Infants with ambiguous genitalia must be immediately assessed by a pediatrician, gynecologist, geneticist, and endocrinologist.
  • The diagnosis of congenital labial hypertrophy and labial adhesions is essentially clinical.

Atrophy of the vulva

• Diagnosis relies on careful clinical and histologic evaluation in order to differentiate the condition from lichen sclerosus and other problems that may cause vulvar atrophy.

TREATMENT, FOLLOW-UP, AND PREVENTION

Section 7 of 10  

• Authors and Editors
• Introduction
• Etiology and Pathophysiology
• Clinical History and Physical Findings
• Histologic Findings
• Differential Diagnosis and Workup
• Treatment, Follow-up, and Prevention
• Conclusions
• Multimedia
• References

Nonneoplastic epithelial disorders

Inflammatory diseases

• Lichen sclerosus
• • Currently, potent topical corticosteroids provide the best outcomes. Clobetasol propionate 0.05% ointment, applied twice daily for 1-3 months (with the dose gradually tapered) provides short-term relief and long-term control in most patients. Maintenance therapy with 1-2 applications per week may be useful. Once daily application of mometasone furoate 0.1% cream may be an option, but its efficacy compared to ultrapotent topical steroids has not been assessed in double-blind comparison trials.
  • Long-term sequelae of potent topical corticosteroids (eg, atrophy and thinning of skin and subcutaneous tissues) have not been clinically significant in persons with this disorder. A protective effect from malignant evolution has been suggested but not proved.
  • Testosterone propionate 2% in petrolatum has been used, but recent studies have shown that it is only slightly more effective than placebo and that it has many adverse effects (eg, clitoral hypertrophy, increased libido, hirsutism, voice alterations).
  • Encouraging results have been obtained with tretinoin cream 0.025% and systemic acitretin. Close follow-up care is recommended because of the significant risk of developing epithelial cancer.
  • Treatment with twice daily applications of topical calcineurin inhibitors (pimecrolimus 1% cream and tacrolimus 0.1% ointment) is also promising.
  • Alternative treatments include intralesional steroid injections and/or cryosurgery, focal ultrasonography, photodynamic therapy, and surgery.
• Squamous cell hyperplasia
• • Treatment of squamous cell hyperplasia is the same as that for lichen sclerosus and is aimed at halting the itch-scratch-itch cycle. General attention to proper hygiene is suggested.
  • If the skin is moist or macerated, aluminum acetate 5% (Burow) solution applied 3-4 times daily for 30-60 minutes is beneficial.
  • Systemic antihistamines or tricyclic antidepressants, especially when taken at bedtime, may help. For lichen sclerosus, the treatment of choice is a potent corticosteroid cream. In refractory lesions, intralesional injections of triamcinolone acetonide may be an alternative.
• Lichen simplex chronicus (localized neurodermatitis)
• • Treatment includes removal of irritants and/or allergens (if identified), followed by topical application of mild-to-high–potency corticosteroids. Do not use high-potency topical steroids for prolonged periods because of adverse effects.
  • Avoid soaps and cleansing agents other than aqueous cream. Discourage excessive cleaning of the genital area; use of hot water; overheating; and wearing of synthetic, rough, and/or tight clothing.
  • Review all cases after lichenification has resolved because lichen simplex chronicus may be associated with underlying dermatoses (eg, Paget disease, Bowen disease).
• Primary irritant dermatitis
• • Identification and avoidance of the offending irritants is crucial. Symptomatic relief may be obtained with cool sitz baths and an application of Burow solution.
  • Corticosteroid ointments may also be used for short-term treatment.
  • Discourage excessive cleaning with inadequate or aggressive soaps and wearing of tight and/or synthetic fabrics that may cause mechanical irritation and occlusion.
• Intertrigo
• • Gentle cleansing is often enough to elicit considerable improvement or healing.
  • The use of antiseptic solutions (eg, triclosan, chlorhexidine) and/or absorbent powders may also be helpful. Sparingly applied mild topical corticosteroids (eg, hydrocortisone 1%) may be necessary to promptly relieve local symptoms.
  • Instruct patients to avoid tight, hot, synthetic clothing and to keep the area cool and dry in order to stop friction and prevent relapses.
• Allergic dermatitis
• • Treatment starts with identification of the offending agent, followed by environmental control.
  • Oral antihistamines and short-term use of a topical corticosteroid ointment (eg, betamethasone-17-valerate 0.1%, triamcinolone acetonide 0.1%) are usually effective.
• Fixed drug eruption: Identification and elimination of the offending agent is the mainstay of treatment.
• Atopic dermatitis
• • In case of acute rash, a sitz bath or compresses with Burow solution once or twice daily are helpful.
  • Topical steroids, such as betamethasone-17-valerate 0.1% cream, and systemic antihistamines, such as hydroxyzine, are indicated to relieve symptoms.
  • Antibiotics are recommended in cases of secondary infection.
  • Advise patients to avoid using irritating detergents, lotions, or perfumed products, and encourage wearing of cotton undergarments.
• Seborrheic dermatitis
• • Treatment includes Burow solution and short-term, low-potency steroid ointments.
  • Topical antifungals may be helpful because Pityrosporum organisms are thought to play a role in causing the disorder.
• Psoriasis
• • Treatment is aimed at symptom relief, thereby minimizing the scratching and rubbing that stimulate cell turnover.
  • Instruct patients to avoid chemical or mechanical traumas, including use of irritating detergents and tight systemic clothing, in order to minimize symptoms.
  • The treatment of choice is calcipotriene ointment, a topical vitamin D-3 preparation that is effective without the risk of skin atrophy.
  • Low-potency corticosteroid ointments may be used but are seldom effective as monotherapy.
  • Advise patients to avoid tar preparations, which are irritating to the vulvar skin.
  • In severe cases, systemic antipsoriatic agents (eg, cyclosporin, acitretin, methotrexate) may be used.
• Reiter disease
• • Methotrexate is the treatment of choice.
  • Systemic retinoids or cyclosporine and topical corticosteroids may provide some relief.