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Invasive Lymphatic Malformation (Gorham-Stout) of the Pelvis with Prominent Skin Involvement

Authors


Address correspondence to Inês Leite, M.D., Dermatology Department, Hospital Nino Jesus, Avda Menéndez Pelayo, 65 Madrid, Spain, or e-mail: leitehome@sapo.pt.

Abstract

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.

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