Bowen's disease (BD) is an in situ squamous cell carcinoma characterized by reddish, well-defined, scaly, erythematous and eezematous plaques. Human papillomavirus (HPV) infection is associated with BD on the hands and genitalia (1,2). Nail BD presenting with longitudinal melanonychia has frequently been reported to be associated with HPV type 56. We describe here a case of periungual verrucous BD with HPV type 58 infection.
MATERIALS AND METHODSA 36-year-old man suffered an injury to his right middle finger. He then noted a small nodule on the injured finger that slowly increased in size. The patient had neither a significant past medical history nor a signifieant family history. Physieal examination revealed an elevated, well-demarcated, slightly pigmented plaque with a keratotic surface tneasuring 12x7 mm in diameter on the periungual area of his middle finger (Fig. 1 a). The patient reported no subjective symptoms. Histopathological examinations revealed the presence of hyperkeratosis. parakeratosis, papillomatosis, dyskeratotic cells and irregularly arranged tumour cells with atypical nuclei (Fig. Ib). Koilocytosis was seen in some areas. Laboratory tests, including a complete blood cell count and a serum chemistry assay, revealed no abnormalities. The lesion was surgically excised and grafted with full-thickness skin under local anaesthesia. There has been no recurrenee over a 1 -year follow-up period. The resected skin specimen was examined by HPV typing with PCR, in situ hybridization and immunohistochemistry.Formalin-fixed and paraffin-embedded samples were then cut into 10-|im sections. The method used and PCR conditions have all been described previously (3). DNA was extracted using Dexpat' (Takara, Kyoto, Japan). HPV PCR was performed with L1C1/L1C2 consensus primers (4). The PCR products were subjected to direct sequencing. DNA extraeted from bowenoid papulosis of another patient was used as a control, in which HPV type 16 was detected (3).The catalysed signal amplification method (GenPoint System; Dako, Kyoto. Japan) was used for detection of HPV by in situ hybridization (3). Formalin-fixed, paraffin-embedded specimens were used. The probe was a biotinylated high-risk HPV probe cocktail (GenPoint HPV; Dako) that contains type 16, 18. 31. 33, 35, 39, 45, 51, 52. 56, 58, 59 and 68 HPV DNA. Immunohistochemistry was performed using an anti-HPV antibody (K1H8; Dako) and the avidin-biotin complex lnethod.
RESULTSThe amplified PCR products were electrophoresed on 2% agarose gel, and a PCR band was seen at the expected position of 256 bp. The PCR product was analysed by direct DNA sequencing, which revealed that the sequence corresponded to the LI gene of HPV type 58 (GenBank: D90400) (Fig. 2). The sequence of the patient showed one missense mutation that had not been reported previously (data not shown).HPV-58-positive cells with nuclear staining were observed in the upper epidermis and stratum corneum of the lesion by in situ hybridization (Fig. lc). Furthermore, HPV immunohistochemistry revealed that th...