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An. bras. dermatol ; 90(3,supl.1): 10-12, May-June 2015. tab, ilus
Article in English | LILACS | ID: lil-755755

ABSTRACT

Abstract

Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation. We discuss an entirely unique case of Phacomatosis pigmentovascularis with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita, which may represent a heretofore undescribed variant of phacomatosis pigmentovascularis.

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Subject(s)
Humans , Male , Young Adult , Mongolian Spot/pathology , Neurocutaneous Syndromes/pathology , Nevus of Ota/pathology , Port-Wine Stain/pathology , Skin Diseases, Vascular/pathology , Skin Neoplasms/pathology , Telangiectasis/congenital , Neurocutaneous Syndromes/classification , Telangiectasis/pathology
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