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An. bras. dermatol ; 92(2): 243-245, Mar.-Apr. 2017. graf
Artigo em Inglês | LILACS | ID: biblio-838052

RESUMO

Abstract: Vulvar cancer accounts for less than 1% of malignancies in women. Verrucous carcinoma of the vulva is a rare histological variation, comprising less than 1% of vulvar cancer cases. Although it is characterized as being locally invasive, the condition is not associated with metastatic spreading. Lesions present in the form of a verrucous, ulcerated, and bleeding tumor that can reach large dimensions. This type of tumor can be mistaken for condylomata, both macroscopically and microscopically. We report the case of an 81-year-old patient with a large vulvar tumor presented for eight years, initially considered as a Buschke-Löwenstein tumor. The patient underwent radical vulvectomy with a V-Y advancement flap technique. This type of tumor should be considered by clinicians dealing with condylomatous ulcerative lesions that do not respond to the usual treatment.


Assuntos
Humanos , Feminino , Idoso de 80 Anos ou mais , Neoplasias Vulvares/patologia , Carcinoma de Células Escamosas/patologia , Carcinoma Verrucoso/patologia , Tumor de Buschke-Lowenstein/patologia , Retalhos Cirúrgicos , Vulva/patologia , Neoplasias Vulvares/cirurgia , Carcinoma de Células Escamosas/cirurgia , Resultado do Tratamento , Carcinoma Verrucoso/cirurgia , Diagnóstico Diferencial
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