Invasive Lymphatic Malformation (Gorham-Stout) of the Pelvis with Prominent Skin Involvement
Article first published online: 24 JUL 2012
© 2012 Wiley Periodicals, Inc.
Volume 30, Issue 3, pages 374–378, May/June 2013
How to Cite
Leite, I., Hernández-Martín, A., Colmenero, I., López-Gutiérrez, J. C. and Torrelo, A. (2013), Invasive Lymphatic Malformation (Gorham-Stout) of the Pelvis with Prominent Skin Involvement. Pediatric Dermatology, 30: 374–378. doi: 10.1111/j.1525-1470.2012.01814.x
- Issue published online: 26 APR 2013
- Article first published online: 24 JUL 2012
Abstract: Gorham-Stout syndrome is a rare disease characterized by progressive osteolysis leading to disappearance of the bone. Vascular proliferations have been implicated in the pathogenesis of this syndrome. The case of a 7-year-old girl with a prominent invasive lymphatic malformation on the lumbosacral area and massive osteolysis of the pelvic girdle is reported.