Kaposiform Hemangioendothelioma (KHE) is a rare vascular tumour of the infancy and the first decade of life. It is locally aggressive and potentially life threatening when associated with consumptive coagulopathy, known as Kasabach-Merritt syndrome (KMS). No consensus or guideline for the therapy has been reached because of the lack of prospective trials, and the different standard care suggestions are based on retrospective case series.

Successful Management of Kaposiform Hemangioendothelioma with Long-Term Sirolimus Treatment: a Case Report and Review of the Literature

Di Carlo, Daniela;Zaccaron, Ada;Parisi, Alice;Cesaro, Simone
2018-01-01

Abstract

Kaposiform Hemangioendothelioma (KHE) is a rare vascular tumour of the infancy and the first decade of life. It is locally aggressive and potentially life threatening when associated with consumptive coagulopathy, known as Kasabach-Merritt syndrome (KMS). No consensus or guideline for the therapy has been reached because of the lack of prospective trials, and the different standard care suggestions are based on retrospective case series.
2018
Kaposiform Hemangioendothelioma; Kasabach-Merrit syndrome; Prednisone; Sirolimus; Vincristine
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/990438
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