Abstract

Vulvar Verrucous Carcinoma (VVC) is a rare lesion, with few described cases. It has low metastatic potential with high morbidity due to the necessity of extensive resections, although. Previously, VVC was considered a synonym to the Buschke-Lowenstein Tumor (BLT) or Giant Condyloma Acuminatum (GCA). Lichen Sclerosus (LS) is associated with Vulvar Intraepithelial Neoplasia (VIN) and Vulvar Squamous-cell carcinoma (SCC); association with VVC is also described. The case of a 60-year-old menopausal woman is reported; she had chronic itching and an extensive verrucous lesion in vulva, initially diagnosed and treated as condyloma acuminatum; there was recurrence as verrucous carcinoma associated to LS. Excision with margins was performed and clobetasol and imiquimod were used. Patient had complete remission with no further recurrences. Distinction between VVC and BLT can be difficult; current literature considers them different entities. Human papillomavirus (HPV) infection and the presence of LS play a controversial role in these injuries.

Highlights

  • In 1948, Ackerman described the first case of verrucous carcinoma (VC) as a variant of a squamous-cell carcinoma (SCC), in oral cavity [1]

  • 154 Verrucous carcinoma of vulva associated with lichen sclerosus and condyloma: case report considered a rare disease; occurrence records consist of some series and case reports [3,4,5]

  • Condyloma Acuminata (GCA) and Verrucous Carcinoma (VC) can be difficult, especially in the context of Lichen Sclerosus (LS), in which the epithelial changes that occur are common to BuschkeLowenstein Tumor (BLT) and VC [6,9,10]

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Summary

Brazilian Journal of Case Reports

Verrucous carcinoma of vulva associated with lichen sclerosus and condyloma: case report.

Introduction
Case report
Findings
The clinical and histopathological distinction between
Full Text
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