SCC in situ ยท MucosalICD-10 D07.1

Vulvar intraepithelial neoplasia

VIN; vulvar HSIL (high-grade squamous intraepithelial lesion); usual VIN (uVIN, HPV-related); differentiated VIN (dVIN, non-HPV / lichen-sclerosus-related); Bowen's disease of the vulva (older term)

Vulvar intraepithelial neoplasia (VIN) is squamous cell carcinoma in situ of the vulva, divided into two biologically distinct entities: usual VIN (uVIN / vulvar HSIL), driven by high-risk human papillomavirus (especially HPV-16) and presenting in younger women as multifocal, often pigmented papules and plaques; and differentiated VIN (dVIN), arising in a background of lichen sclerosus or lichen planus in older post-menopausal women as subtle thickened, erythematous or leukoplakic plaques. The two have very different progression risks: uVIN progresses to invasive SCC in ~10% over years, while dVIN has a much higher (32โ€“86%) and more rapid progression to invasive vulval SCC. Diagnosis requires biopsy and management is best coordinated through a vulval MDT.

CurrentLast reviewed 26 April 2026

Subtypes

  • Usual VIN (uVIN / vulvar HSIL) โ€” HPV-driven (especially HPV-16). Younger women (30sโ€“50s); multifocal pigmented or red papules / plaques; smoking and immunosuppression are key cofactors. Lifetime invasive risk ~10% (treated) / ~25% (untreated).
  • Differentiated VIN (dVIN) โ€” non-HPV; arises within lichen sclerosus or lichen planus. Older post-menopausal women; subtle thickening, leukoplakia or erythema; progression to invasive SCC in 32โ€“86% over a few years if untreated. Most under-diagnosed and most aggressive form.
  • Bowenoid papulosis โ€” small multiple pigmented HPV-driven papules in young adults; histologically resembles VIN but generally regresses; see monograph.

Clinical features

  • Pruritus, soreness, dyspareunia, bleeding, dysuria.
  • Asymptomatic in some โ€” incidental finding at examination.
  • uVIN: multifocal pigmented or red papules/plaques on vulva, perineum, perianal skin.
  • dVIN: ill-defined leukoplakic, erythematous or hyperkeratotic patch within lichen sclerosus field; any new induration or thickening in LS warrants biopsy.
  • Examine the entire anogenital area, vagina and cervix โ€” synchronous lesions common in HPV-related disease.

Diagnosis

  • Punch biopsy under local anaesthetic โ€” adequate depth essential to assess for early invasion.
  • Multiple biopsies if multifocal or extensive disease.
  • Histology distinguishes uVIN (full-thickness atypia, koilocytes, p16 strongly diffuse positive) from dVIN (basal-cell atypia with maturation, p53 aberrant, p16 negative).
  • HPV typing in equivocal cases.
  • Cervical screening up to date.
  • HIV testing in selected patients.

Management

  • Refer to vulval MDT.
  • uVIN / HSIL:
    • Wide local excision with histological clearance is standard for unifocal disease.
    • Topical imiquimod 5% โ€” 3 nights/week for 12โ€“16 weeks; complete response 30โ€“60%; useful for multifocal disease, sparing tissue.
    • Topical 5-fluorouracil โ€” alternative.
    • COโ‚‚ laser ablation โ€” destruction without histology; reserved for confirmed VIN with no suspicion of invasion.
    • Photodynamic therapy in selected cases.
  • dVIN:
    • Wide local excision with clear margins is the only acceptable treatment given high progression risk; topical / ablative therapies inappropriate.
    • Concurrent management of underlying lichen sclerosus with ultrapotent topical steroid.
    • Lower threshold for re-excision and surveillance.
  • Surveillance: lifelong; 3-monthly for 12 months, then 6-monthly. Concurrent cervical screening.
  • HPV vaccination has a primary prevention role; may have secondary prevention role to reduce recurrence after treatment for HPV-related disease (emerging data).

Prognosis

uVIN โ€” recurrence ~30%, progression to invasive SCC ~10% (treated) / ~25% (untreated). dVIN โ€” high progression risk (up to 86% if untreated); requires aggressive surgical management. Long-term surveillance is essential. Smoking cessation and treatment of LS reduce recurrence and progression.

References

  1. Bornstein J et al. The 2015 ISSVD terminology of vulvar squamous intraepithelial lesions. Obstet Gynecol; 2016.
  2. Edwards SK, Lewis F, Fernando I, Haddon L, Grover D. 2024 British Association for Sexual Health and HIV UK national guideline on the management of vulval conditions. Int J STD AIDS. 2025.

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