Phacomatosis pigmentovascularis is a rare syndrome, defined as the simultaneous presence of vascular nevus and melanocytic nevus in the same patient. We report the case of a 53-year-old woman presented with dermal melanosis and extensive vascular nevus, which match the typical manifestations of phakomatosis pigmetovascularis of cesioflammea type, according to Happle’s classification. The rare occurrence of this genodermatosis and the clinical exuberance of the skin lesions motivated this case report.
CITATION STYLE
Villarreal, D. J. V., & Leal, F. (2016). Phacomatosis pigmentovascularis of cesioflammea type. Anais Brasileiros de Dermatologia, 91(5), 54–56. https://doi.org/10.1590/abd1806-4841.20164516
Mendeley helps you to discover research relevant for your work.