Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome
- PMID: 15575847
- DOI: 10.1111/j.0736-8046.2004.21605.x
Phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome
Abstract
We describe a 23-month-old child with phakomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome. Phakomatosis pigmentovascularis type IIb is a rare cutaneous malformation characterized by the simultaneous occurrence of nevus flammeus and melanocytic nevi. A brief review of the literature is presented and classification of this rare disease is discussed.
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