Condition
Kaposiform Hemangioendothelioma with Kasabach-Merritt Syndrome
Kaposiform hemangioendothelioma is a rare, aggressive vascular skin, tissue and bone tumor found in children. It’s characterized by nodules and sheets of spindle cells that become warped in the extremities, chest and abdomen causing the blood vessels to expand. Although a relatively rare condition, the increasing number of reports on kaposiform hemangioendothelioma in infants and children is often complicated by rapidly growing lesions, also known as Kasabach-Merritt syndrome (KMS).
Meet the Providers Who Treat Kaposiform Hemangioendothelioma with Kasabach-Merritt Syndrome
Finn's Story
When Finn was born, his parents and doctors immediately knew something was wrong. Finn's left leg was swollen to the size of an adult head, and it continued to swell at an alarming rate.
Departments that Treat Kaposiform Hemangioendothelioma with Kasabach-Merritt Syndrome
General and Thoracic Surgery
The pediatric surgical experts at Children's National in Washington, D.C., provide advanced, comprehensive surgical care for infants, children and teenagers.