Vulvar Disease
Ayman Ewies
Consultant Gynaecologist
The Ipswich Hospital
24
th
April 2009
2
Role of Colposcopy
Assessment of:
1.VIN.
2.Carcinoma.
Classification of the International Society for
Study of Vulvar Diseases (ISSVD)
Non Neoplastic Epithelial
Disorders
VIN Carcinoma
Lichen Scelerosis Squamous Intra-epithelial
Neoplasia: VIN I-III
Squamous Cell Hyperplasia Non squamous Intra-epithelial
Neoplasia:
-Paget’s disease
-Melanoma in situ
Other Dermatoses
Vulvar Intra-epithelial Neoplasia
VIN
5
Incidence & Risk Factors
Incidence:
–VIN I & II is unknown
–VIN III: 2.1/10 000
Common sites:
1.Posterior fourchette.
2.Perineum.
3.Around the clitoris.
4.Lower part of labia majora and labia minora.
5.Older women often have a single lesion, while younger women
(under the age of 50) tend to have multi-focal disease.
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Signs
The clinical appearance is variable.
Typically lesions are:
–Papular with sharp borders.
–Keratotic rough surfaces.
Sometimes, they resemble condyloma accuminata.
The colour may be white, red or brown.
Cervical cytology, colposcopy and vaginoscopy are
indicated in all cases
Choice depends on:
1.Site.
2.Size.
3.Focality.
4.Grade.
5.Age and General condition.
(preservation of appearance and function of the vulva as
well as the psychological issues should be
considered)
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Treatment VIN I & II
Surveillance with vulvoscopy & biopsies
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Treatment VIN III
Medical:
1.5-FU.
2.Imiquimod
3.α-interferon.
Laser ablation (CO
2):
•High recurrence rate especially in hair-bearing skin.
•It may be better in young women, particularly, for small areas of peri-
urethral and peri-clitoral disease.
Surgical:
1.Laser excision.
2.Wide local excision with knife (appropriate in the majority of cases).
3.Simple vulvectomy (in a minority of selected cases).
4.Skinning vulvectomy and skin grafting.
An excision margin of 5 mm of healthy tissue is recommended to reduce risk of
recurrence
Lichen Sclerosus (LS)
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Lichen Sclerosus
It is an inflammatory skin disorder whose underlying cause
is not known.
–It probably has an auto-immune origin with seemingly genetic
predisposition.
It is usually seen in the elderly but can occur at young ages.
The associated atrophic changes are reversible.
The life time risk of developing vulvar carcinoma is 3-5%.
It is found adjacent to 60% of vulvar cancer cases.
The common sites:
1.Labia minora.
2.Inner surfaces of labia majora.
3.Clitoris.
4.Perineum.
5.Perianal area.
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Signs
The classical clinical appearance:
1.Ivory pallor of the vulva with epidermal atrophy
giving a parchment-like wrinkled surface.
2.Loss of elasticity.
3.Fissuring.
As the disease progresses:
1.The architecture of the vulva is distorted.
2.Resorption and fusion of labia minora.
3.Loss of clitoral hood.
4.The epithelial surface becomes waxy, shiny and
speckled.
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Diagnosis
Although the clinical features are often straight forward,
biopsy is mandatory:
1.To confirm the diagnosis.
2.To rule out underlying VIN or micro-invasive
disease.
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Treatment
Aims:
1.Relief of symptoms.
2.Prevention of progression.
Potent topical corticosteroids with maintenance therapy at the lowest
possible dose.
The patient should be advised to use treatment only on the affected
areas and could use a mirror if necessary.
Treatment is recommended if there are clinical signs even in absence of
symptoms.
Long-term follow-up is required in view of possible malignant
potential.
Vulvoscopy
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Indications for referral
1.Colour changes e.g. whitening, pigmentation, redness, etc.
Vulvar lesions are difficult to assess because:
1.They do not have a typical appearance.
•Histologically identical lesions can have varied
appearances.
2.The vulva is less likely to stain with acetic acid and
toluidine blue.
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Vulvoscopic Examination
Clean the vulva with normal saline.
Apply 3-5% acetic acid (for 2-5 minutes since the lesion
appears late):
1.The thick hair-bearing epithelium, e.g. external surface of the labia
majora, does not exhibit features of vascular aberration (mosaicism
and punctation).
2.In the non-hair bearing parts, e.g. labia minora and the vestibule,
the skin is thinner aceto-whitness, punctation and mosaicism can
be identified.
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Vulvoscopic Examination
Collin’s Test
Toluidine blue, a nuclear stain, can be used to mark vulvar
lesions.
While the test lacks specificity it can be helpful in
identifying areas for appropriate biopsy.
1.Clean the vulva with normal saline.
2.Apply aqueous toluidine solution (1%) for 2 minutes.
3.Rinse the area with acetic acid 1%.
4.Abnormal cells with high nuclear content retain the blue
stain.
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Vulvar Biopsies
All lesions should be biopsied.
The biopsy should include the area of transition from
normal to abnormal tissue.
Keyes punch forceps is a suitable method for office
biopsy:
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Vulvar Biopsies
Keyes punch forceps:
Removes 3-6 mm of skin.
The depth depends on the pressure
applied.
The biopsy site can be left to heal
spontaneously (2 weeks|).
Haemostasis can be achieved by:
1.Monsel’s solution.
2.Silver nitrate.
3.Diathermy.
4.Sutures.