Resumo

ANDREA, Soto; EMILIA, Villani Maria; FABIO, Muñoz  e  GLADYS, Merola. Parkes Weber syndrome. Rev. argent. dermatol. [online]. 2023, vol.104, pp.91-100. ISSN 1851-300X.

Parkes Weber Syndrome is characterized by overgrowth of a limb with capillary, venous, lymphatic, and arteriovenous malformation. We present the case of a 23-year-old patient who came to the dermatology service for an ulcer on congenital capillary malformation.We were able to arrive at the diagnosis using various imaging studies, while the therapeutic measure, with the character of tertiary prophylaxis, consisted of multiple embolizations.

Palavras-chave : Parkes Weber syndrome; arteriovenous shunts.