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Two Reports of Phacomatosis Pigmentovascularis Type Iib, One in Association with Sturge–Weber Syndrome and Klippel–Trenaunay Syndrome
Author(s) -
Finklea Lindsey B.,
Mohr Melinda R.,
Warthan Molly M.,
Darrow David H.,
Williams Judith V.
Publication year - 2010
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/j.1525-1470.2010.01144.x
Subject(s) - sturge–weber syndrome , medicine , klippel trenaunay syndrome , dermatology , pathology , soft tissue
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.