Vulvar Dysplasia and Colposcopy
Introduction
A. Vulvar intraepithelial neoplasia (VIN) is defined as the loss of epithelial
cell maturation with associated nuclear hyperchromoses and pleomorphorism,
cellular crowding and abnormal mitoses.
1. Invasive vulvar cancer has features of VIN with invasion
of cells into the stroma
2. Human papilloma virus (HPV) has papillaform shapes and is covered
with hyperplastic squamous epithelium that possesses hyperkeratosis
and parakeratosis. Human papilloma virus is not characterized by cellular
atypia, but mitosis can be present.
B. Evaluation of the vulva by gross inspection only can miss detection
of acetowhite lesions or other less macroscopic lesions.
Etiology, Incidence, and Clinical Characteristics
A. VIN is part of a syndrome of multifocal epithelial changes of the anogenital
tract.
B. Risk factors are similar to those for cervical dysplasia.
1. early age of sexual intercourse
2. multiple sexual partners
3. altered immune system
4. association with high risk HPV types
5. a history of smoking
C. Sturgeon et al found that from 1973-1987, there was a doubling of the
annual incidence of VIN from 1.1 to 2.1/100,000 women years. White women
less than 35 years of age had the greatest increase. Peak in-situ incidence
shifted from women greater than 54 years to women aged 35-54.
D. Crum found that women with VIN and aged 35-55 are more likely to
have previous HPV, sexual transmitted diseases (STDs), preexisting VIN,
a high association with cervical neoplasia, and smoking. The opposite was
true for women greater than 55 years.
E. Greater than 50% of patients presenting with vulvar dysplasia are
without symptoms.
F. Of patients with symptoms, pruritis is the most common.
Diagnosis
A. The key to diagnosis of VIN is a high index of suspicion.
B. Definitive diagnosis is made by colposcopic evaluation followed
by biopsy.
C. The colposcopic technique differs slightly from cervical or vaginal
colposcopic exam.
1. 3-5% acetic acid must be applied 3-5 minutes in advance
to allow for absorption through the keratinized surface of the vulvar skin.
2. After adequate acetic acid soaks, careful examination is performed
of the vulvar folds, perineal body, and the perianal and anal regions.
3. Involved regions and planned biopsy sites should be mapped.
4. The biopsy site is infiltrated with 1-2% xylocaine.
5. Biopsy is easily attained with Keyes punch or excisional technique.
D. In the past, toluidine blue was used to stain the vulva. This nuclear
stain can detect areas of superficial epithelial high-grade lesions. However,
there is a high incidence of false positive results, especially at excoriated
or erosive sites.
Vulvar Lesions
A. White lesions
1. Leukoplakia, lesions that are white prior to application
of acetic acid, come from a thick hyperkeratotic layer on the epithelial
surface.
2. Acetowhite lesions with irregular geographic borders can represent
flat condyloma, VIN, or prolonged application of acetic acid on normal
vulva. The more intense, irregular, and raised the change, the more likely
it is to be associated with HPV or dysplasia.
B. Red lesions
1. Occur in the absence of a hyperkeratotic layer.
2. Nuclei are retained through to the epithelial surface -- parakeratosis.
3. Paget's disease is a classic example of this change. Its appearance
is frequently multifocal red lesions with islands of white hyperkeratotic
epithelium on the surface.
4. Ulcerative lesions also may be red in appearance. These lesions
may herald an invasive malignancy.
C. Pigmented lesions occur because of rapid epithelial proliferation.
1. The pigmentation is carried from the basal layer to the
surface.
2. Condyloma can exhibit a surface pigmentation change.
3. More commonly, pigmentation is associated with dysplastic, multifocal
vulvar, or perianal/anal lesions.
D. Vascular patterns are not common on the vulva secondary to the increased
keratin layer. Punctation occasionally occurs on the mucosal surfaces of
the vestibule and labia minora.
Summary
Colposcopy is particularly helpful in the diagnosis of VIN and invasive
cancer. VIN associated with HPV is more frequent in younger women, less
likely to be invasive, and more often multifocal. White, red, and hyperpigmented
lesions are associated with VIN and vulvar cancer. Biopsy is required for
definitive diagnosis.