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KHE is an uncommon vascular tumor that can be present at birth or appear in early infancy. Compared with common hemangiomas, KHE occurs less frequently in the head and neck region; typical locations are the trunk, shoulder, thigh, and retroperitoneum.
The involved skin is deep reddish-purple, tense, and shiny. Tiny purple or red spots and a bruise-like discoloration overlie and are adjacent to the tumor. This bruised appearance may falsely suggest a diagnosis of child abuse.
KHE is often associated with the Kasabach-Merritt phenomenon, as noted above bleeding disorder. Retroperitoneal KHE is associated with a high mortality rate. KHE sometimes responds to corticosteroid; often vincristine is needed to control the tumor and correct the bleeding disorder.
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