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                     Bowenoid Papulosis

         Dr Sampurna Roy MD

 
 
 Infectious Disease Online

          

http://www.histopathology-india.net/Infection.htm

                

Bowenoid papulosis is a lesion which usually occurs on the genitalia, and presents as a solitary or multiple verruca-like papules or plaques.

Image1  ;  Image2 ;   Image3 ;  Image4 ;  Image5 ;  Image6 ; Image7  ; Image8 (fujita-hu.ac.jp. Dr Tsutsumi)

Sometimes there is a history of a previous condyloma.

Bowenoid papulosis  has a close histological resemblance to Bowen's disease.

Age & sex : Bowenoid papulosis has a predilection for  young sexually active adults. The male to female ratio is equal.

Site: In males involves the glans penis and also the foreskin. In females the vulval lesions are often multiple, bilaterial and pigmented. They resemble verrucae, small condylomas or nevi.

Extragenital sites include neck, face and fingers.

Anal lesion: Anal intraepithelial neoplasia (AIN) presenting as bowenoid papulosis and perianal Bowen's disease is a precursor lesion for invasive squamous cell carcinoma.

Causative organisms : Most cases of bowenoid papulosis are due to HIV-16.

In few cases  HPV-18, 35 and 39, or mixed infections, have been present.

HPV-16 strain has also been implicated in the pathogenesis of vulval carcinomas and cervical intraepithelial neoplasia.

Anogenital cancers have been associated with the above mentioned HPV types together with more recently identified types such as HPV-30, 31, 33, 45, 51, 52, 56, 58, 66 and 69.

Microscopic features: Image Link  

- The histological differentiation of bowenoid papulosis and Bowen’s disease is difficult.

- Bowenoid papulosis is characterized by full-thickness epidermal atypia and loss of architecture.  The epidermal atypia is sometimes known as bowenoid dysplasia.         

- The basement membrane is intact. 

- Mitoses are frequent, sometimes with abnormal forms.

- Dyskeratotic cells are also present. 

- True koilocytes are rare. Partly vacuolated cells are sometimes present.

- The stratum corneum and granular cell layer often contain small inclusion-like bodies.

- Inclusion bodies are deeply basophilic, rounded and sometimes surrounded by a halo.

- These inclusion bodies, together with the numerous metaphase mitoses, are the features that suggest a diagnosis of bowenoid papulosis rather than Bowen’s disease.

- The type VIN (vulvar intraepithelial neoplasia) designated as Bowenoid Papulosis show a degree of cytological atypia approaching that of Bowen's disease. In Bowenoid keratosis the dysplastic cells are present in a backround of relatively orderly epithelial maturation and that the acrotrichium is usually spared.

Fate:

- Lesions are often resistant to treatment and may have a protracted course, usually in older patients and in those with depressed immunity.

- Some of these lesions persist for more than 5 years and may never regress completely

- In a number of young patients spontaneous regression occurs within few months.

- In a small number of cases invasive carcinoma develops. The risk of carcinomais greatest in women over age of 40. It may also occur in men. It has been suggested that a cocarcinogenic factor, may lead to malignant transformation. 

- In the vulva, spontaneous regression has been observed and response to conservative therapy is the rule even if recurrences are common.

      

Extragenital bowenoid papulosis associated with atypical human papillomavirus genotypes.J Cutan Med Surg. 2002 Mar-Apr;6(2):117-21.

BACKGROUND:

Bowenoid papulosis typically appears as grouped violaceous or red-brown papules in the genital or perianal regions and clinically resembles condylomata acuminata. Isolated extragenital bowenoid papulosis is rare and has been reported in only a few case reports.

OBJECTIVES:

A 51-year-old immunocompetent, healthy woman had two solitary papules on the elbow; a 41-year-old HIV-positive man had a solitary cutaneous plaque on the abdomen. No genital, periungual, or other extragenital sites of involvement were noted in either patient. The diagnosis was confirmed histologically in both cases. Lesional skin from the female patient was tested with the Digenehybrid HPV DNA assay and was positive for a mixture of low-risk HPV subtypes (6, 11, 42, 43, 44). Lesional skin from the male patient was tested with polymerase chain reaction (PCR). Consensus primers targeted for the HPV L1 region, which is a highly conserved sequence common to more than 20 HPV subtypes encoding a viral capsid protein, were used. PCR using the consensus primers was positive, but type-specific probes for HPV types 6, 11, 16, 18, 45, 31, 33, 35, and 39 were negative.

CONCLUSIONS:

To our knowledge, our male patient represents the first case of isolated bowenoid papulosis of the abdominal skin. Isolated upper-extremity bowenoid papulosis in our female patient is also a unique case in both location and involvement of low-risk HPV types (6, 11, 42, 43, 44), which have not been previously associated with extragenital bowenoid papulosis.

Abstracts:

P16(INK4A) expression in Bowen's disease and Bowenoid papulosis.
J Med Assoc Thai. 2006 Sep;89(9):1460-5.

Detection of mucosal human papilloma virus DNA in bowenoid papulosis, Bowen's disease and squamous cell carcinoma of the skin.
J Dermatol. 2006 May;33(5):331-7.

Skin Pathology- Weedon D, 2nd Ed.Churchill Livingstone.Pg 705.

Differential diagnosis of chronic perianal dermatitis. Premalignant and malignant disorders.Hautarzt. 2004 Mar;55(3):266-72

Morphometric assessment of nuclei in Bowen's disease and bowenoid papulosis.Skin Res Technol. 2004 Feb;10(1):67-70

Bowenoid papulosis at the site of prior herpes progenitalis.Skinmed. 2004 Nov-Dec;3(6):347-9.

Bowenoid papulosis. Classification as a low-grade in situ carcinoma of the epidermis on the basis of histomorphologic and DNA ploidy studies.Anal Quant Cytol Histol. 1989 Dec;11(6):419-25

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