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Advisor(s)
Abstract(s)
Phacomatosis pigmentovascularis is a rare syndrome characterized by the coexistence of a pigmented nevus and a cutaneous vascular malformation. We report a 5-year-old boy with all the typical findings of phacomatosis pigmentovascularis type Ia. Although its existence according to the traditional classification has been questioned, this case represents a very rare association of a capillary vascular malformation and a common keratinocytic nevus of the soft type.
Description
Keywords
HCC DER Vascular Malformations Phakomatoses Neurocutaneous Syndromes
Citation
Case Rep Dermatol Med. 2014;2014:437085