Penile Cancer: Benign & Premalignant Penile Tumors

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Benign Penile Tumors[edit | edit source]

Pearly penile papules[edit | edit source]

  • Also known as papillomas
  • Normal and generally found on the glans penis or corona
  • Insert figure

Zoon balanitis[edit | edit source]

  • Also called plasma cell balanitis and balanitis plasmacellularis
  • Occurs in uncircumcised men from the 3rd decade onward
  • Appearance: smooth, moist, erythematous, well-circumscribed plaques on the glans penis; shallow erosions are often present and lesions can be quite large (up to 2cm); difficult to distinguish from carcinoma in situ
    • See Figure
  • Pathology:
    • Angiofibromas, similar to the lesions seen on the face in tuberous sclerosis
    • Plasma cell infiltrate
  • Diagnosis and evaluation: biopsy
    • Malignancy and extra-mammary Paget’s disease must be excluded
  • Management
    • Circumcision
      • Curative in the majority of cases
      • Prevents against development of the disease
      • For patients wanting to avoid circumcision, topical corticosteroids may provide symptomatic relief; topical calcineurin inhibitors (tacrolimus or pimecrolimus) and laser therapy may also play a role

Premalignant Cutaneous Penile Lesions[edit | edit source]

  • Classified as HPV-related vs. non-HPV related§
    • HPV related (3): bowenoid papulosis, verrucous carcinoma, CIS
      1. Bowenoid papulosis
        • Appearance: multiple reddish-brown verrucous papules on the penile skin; occurs on the shaft of young men in most cases
          • See Figure
        • Histologically similar to low-grade carcinoma in situ [Bowen’s disease]
        • HPV 16 has been suspected as a cause
        • Progression rate to invasive cancer: 1%
        • Diagnosis: biopsy (gold standard)
        • Management: options include excision, electrocautery, cryotherapy, laser, or 5-fluorouracil topical therapy
      2. Verrucous carcinoma (also known as classic Buschke-Löwenstein Tumor and giant condyloma)
        • DNA from HPV types 6 and 11 has been identified in these tumors
        • Progression rate to invasive cancer: 30%
          • Exhibits progressive local growth but does not metastasize
          • Results in invasion and destruction of adjacent tissues by compression
            • Buschke-Löwenstein tumor differs from condyloma acuminatum in that condylomata, regardless of size, always remain superficial and never invade adjacent tissue.
        • Management: often requires surgical excision for definitive treatment; radiation is ineffective
        • INSERT FIGURE
      3. CIS
        • Erythroplasia of Queyrat
          • CIS of the glans or foreskin/span>
          • Progression rate to invasive cancer: 30%
        • Bowen’s disease
          • CIS the penile shaft or the remainder of the genitalia or perineal region/span>
          • Progression rate to invasive cancer: 5%
          • See Figure
        • Metastasis extremely rare
        • Not associated with visceral malignancies
    • Non-HPV related (5):
      1. Penile Kaposi sarcoma
        • Often associated with herpes-virus 8
        • Should prompt an investigation into whether patient is also infected with HIV or otherwise immunosuppressed
        • Appears as a raised, painful, bleeding papule or ulcer with bluish discolouration
          • See Figure
        • Categories of Kaposi sarcoma (4):
          1. Classic: occurs in patients without known immunodeficiency and typically has an indolent course
          2. Immunosuppressive treatment-related: occurs in patients undergoing immunosuppression for organ transplantation or other reasons
          3. African Kaposi sarcoma: occurs in young men and can be indolent or aggressive
          4. Epidemic or HIV-related: occurs in patients with AIDS
          • The classic and immunosuppressive forms of the disease are considered non-epidemic
            • Non-epidemic Kaposi sarcoma limited to penile involvement should be aggressively treated because it is rarely associated with diffuse organ involvement
        • Management
          • The first step in treatment of Kaposi's sarcoma in patients with HIV is to initiate HAART or to optimize the HAART regimen, which generally results in remission of Kaposi's sarcoma.
          • Local treatment can include laser therapy, cryotherapy, surgical excision, application of topical retinoids.
          • Disseminated or visceral Kaposi's sarcoma is treated with combination chemotherapy.
      2. Penile cutaneous horn
        • Rare
        • Usually develops over a pre-existing skin lesion (wart, nevus, traumatic abrasion, or malignant neoplasm)
        • Characterized by overgrowth and cornification of the epithelium, which forms a solid protuberance
          • See Figure
        • May recur and may demonstrate malignant change on subsequent biopsy, even when initial histological appearance is benign. As a result, careful histological evaluation of the base and close follow-up of the excision site are essential
      3. Leucoplakia
      4. Lichen sclerosis (see Penis and Urethra Surgery Chapter Notes)
      5. Pseudoepitheliomatous micaceous and keratotic balanitis

References[edit | edit source]

  • Wein AJ, Kavoussi LR, Partin AW, Peters CA (eds): CAMPBELL-WALSH UROLOGY, ed 11. Philadelphia, Elsevier, 2015