Two reports of phacomatosis pigmentovascularis type IIb, one in association with Sturge-Weber syndrome and Klippel-Trenaunay syndrome

Pediatr Dermatol. 2010 May-Jun;27(3):303-5. doi: 10.1111/j.1525-1470.2010.01144.x.

Abstract

We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge-Weber syndrome and Klippel-Trenaunay syndrome. To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge-Weber syndrome and Klippel-Trenaunay syndrome in the English language literature.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Humans
  • Infant
  • Infant, Newborn
  • Klippel-Trenaunay-Weber Syndrome / diagnosis*
  • Male
  • Neurocutaneous Syndromes / diagnosis*
  • Sturge-Weber Syndrome / diagnosis*
  • Vascular Malformations / diagnosis*