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HEALTH PROFESSIONAL · SOURCE READING

Treatment Options for Vulvar Intraepithelial Neoplasia (VIN)

Source: Vulvar Cancer Treatment (PDQ®)–Health Professional Version, National Cancer Institute.

Source updated: May 14, 2025 · Captured 2026-09-09.

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Context: Treatment of Vulvar Intraepithelial Neoplasia

Treatment options for VIN include:

Surgery.

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Surgery.

Separate excision of focal lesions.[1]

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Surgery.

Wide local excision.[1]

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Surgery.

Carbon dioxide (CO2) laser surgery and vaporization.[2,3] A disadvantage of vaporization is that it does not provide tissue for histological examination to confirm complete removal of the lesion and the absence of invasive disease.

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Surgery.

Ultrasonic surgical aspiration.[2,3]

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Surgery.

Superficial skinning vulvectomy with or without grafting.[1]

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Topical imiquimod for patients who want to avoid surgery.[4-8]

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Traditionally, there were three grades of VIN, however, there is little evidence that all three grades are part of the same biological continuum or that grade 1 is even a cancer precursor. In 2004, the International Society for the Study of Vulvovaginal Disease (ISSVD) changed its terminology, reserving the designation VIN for two categories of lesions based on morphological appearance.[9] In 2015, the ISSVD developed terminology for vulvar squamous intraepithelial lesions (SIL), which includes:[10]

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Low-grade SIL of the vulva (vulvar LSIL) encompasses flat condyloma or human papillomavirus effect.

High-grade SIL (vulvar HSIL) was termed VIN, usual type in the 2004 ISSVD terminology.

VIN, differentiated type.

High-grade VIN is usually managed with active therapy because of a higher risk for progression to invasive disease.[2] Estimates of progression rates are imprecise. A systematic literature review that included 88 untreated patients with VIN 3 reported a 9% progression rate (8 of 88 patients) to invasive vulvar cancer during 12 to 96 months of observation. In the same review, the spontaneous regression rate was 1.2%, all of which occurred in women younger than 35 years.[1] However, in a single-center study, 10 of 63 (16%) untreated women with VIN 2 or VIN 3 progressed to invasive cancer after a mean of 3.9 years.[11]

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VIN lesions may be multifocal or confluent and extensive. It is important to perform multiple biopsies in treatment planning to exclude occult invasive disease. VIN located in nonhairy areas can be considered an epithelial disease; however, VIN found in hairy sites usually involves the pilosebaceous apparatus and requires a greater depth of excision because it can track along hair roots.

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Preserved source evidence · Not medical advice