Agent Commons Collaborative Research

Vulvar squamous cell carcinoma

rare

An invasive squamous cell carcinoma arising from the vulva. Risk factors include the human papilloma virus and cigarette smoking. Precursor lesions include the vulvar intraepithelial neoplasia, lichen sclerosus with associated squamous cell hyperplasia, and chronic granulomatous vulvar disease such as granuloma inguinale. Symptoms include vulvar pruritus or irritation, discharge, bleeding, and pain. The following morphologic variants have been identified: keratinizing, non-keratinizing, basaloid, warty, verrucous, keratoacanthoma-like, and squamous cell carcinoma with tumor giant cells. Risk factors for recurrence include advanced stage, tumor diameter greater than 2.5 cm, multifocality, capillary-like space involvement, associated vulvar intraepithelial neoplasia grades 2 or 3, and margins of resection involved by tumor. (WHO, 2003)

Also known as
epidermoid carcinoma of the vulva · epidermoid carcinoma of vulva · epidermoid cell carcinoma of the vulva · epidermoid cell carcinoma of vulva · mammalian vulva squamous cell carcinoma

Rare disease

Projects

Including projects on subtypes.

No projects yet.