Pre-malignant ยท HPVICD-10 D07

Bowenoid papulosis

Multifocal HPV-driven anogenital intraepithelial neoplasia in young adults

Bowenoid papulosis is a clinico-pathological entity in which multiple small, pigmented or red papules arise on the anogenital skin of young, otherwise healthy adults, driven by high-risk human papillomavirus (most commonly HPV-16). The defining feature is a striking discordance between an alarming histological appearance โ€” full-thickness keratinocyte atypia indistinguishable from squamous cell carcinoma in situ (Bowen's disease) โ€” and a generally benign clinical course, with frequent spontaneous regression and a low rate of progression to invasive carcinoma. Recognition matters because aggressive surgical management of every lesion is unnecessary; topical or destructive therapy with surveillance is usually appropriate. Sexual partner screening, cervical cytology, HIV screening and HPV vaccination should be considered.

CurrentLast reviewed 26 April 2026
Clinical image of Bowenoid papulosis
Bowenoid papulosis. Image sourced from DermNet New Zealand. Used under CC BY-NC-ND 4.0. No endorsement implied.

Clinical features

  • Multiple (often 4 to 30+) small (2โ€“10 mm) pigmented brown to violaceous papules with a smooth or velvety surface.
  • Distribution: penile shaft and glans (men); vulva, perianal area (women); perianal in both sexes.
  • Median age 25โ€“35; both sexes; sexually active patients.
  • Usually asymptomatic; occasional itch or soreness.
  • Frequently misdiagnosed as warts (condyloma acuminatum), seborrhoeic keratoses, naevi or melanoma.

Differential diagnosis

  • Anogenital warts (condyloma acuminatum) โ€” usually verrucous, skin-coloured to white, less pigmented, low-risk HPV (6, 11).
  • Vulvar / penile intraepithelial neoplasia (VIN, PeIN) โ€” usually fewer, larger, less pigmented lesions; behaves more aggressively. The histological line between bowenoid papulosis and HPV-driven uVIN/PeIN is blurred โ€” the distinction is largely clinical (multifocal small papules in a young patient = bowenoid papulosis; large solitary plaque in older patient = VIN/PeIN).
  • Erythroplasia of Queyrat โ€” solitary or few large red velvety plaque on glans of older uncircumcised man.
  • Bowen's disease โ€” solitary scaly plaque on sun-exposed or anogenital skin of older adult.
  • Pigmented seborrhoeic keratosis, melanocytic naevus โ€” clinical mimics.

Diagnosis

  • Punch biopsy of representative lesion(s).
  • Histology indistinguishable from Bowen's disease โ€” full-thickness keratinocyte atypia with mitoses at all levels โ€” but in a multifocal anogenital field of a young adult.
  • p16 strongly diffuse positive (HPV-driven); high-risk HPV typing (especially HPV-16) supports diagnosis.
  • Examine the entire anogenital area, oral mucosa and assess for cervical disease in women.
  • HIV testing in selected patients.

Management

  • Conservative โ€” many lesions regress spontaneously over months to years, particularly in young patients with intact immunity.
  • Topical 5% imiquimod (3 nights/week for 12โ€“16 weeks) โ€” clearance in 50โ€“80%.
  • Topical 5-fluorouracil โ€” alternative.
  • Cryotherapy, curettage, electrocautery, COโ‚‚ laser โ€” for selected larger/persistent lesions.
  • Surgical excision reserved for atypical, suspicious or refractory lesions.
  • Counsel about sexual transmission, condom use and partner examination.
  • Cervical cytology and HPV screening for the patient and female partners.
  • HPV vaccination โ€” primary prevention for partners and unaffected individuals; may reduce recurrence in treated patients.

Prognosis

Excellent โ€” most cases regress or are cleared with conservative treatment. Progression to invasive squamous cell carcinoma is uncommon in young immunocompetent patients (<5% in older cohorts); modern series including older patients and HIV-positive or otherwise immunocompromised cohorts report progression rates of 10–15%. Long-term surveillance (annual review and prompt biopsy of any persistent or atypical lesion) is appropriate, particularly in immunocompromised patients.

References

  1. Wade TR et al. Bowenoid papulosis of the genitalia. Arch Dermatol; 1979.
  2. Schwartz RA, Janniger CK. Bowenoid papulosis. J Am Acad Dermatol; 1991.

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