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

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.

• Authors: Lindsey B Finklea, Melinda R Mohr, Molly M Warthan, David H Darrow, Judith V Williams
• Journal: Pediatric dermatology (Pediatr Dermatol) Vol. 27 Issue 3 Pg. 303-5 ( 2010) ISSN: 1525-1470 [Electronic] United States
• PMID: 20609155 (Publication Type: Case Reports, Journal Article, Review)

Topics

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