We present a neonate with a cervicofacial haemangioma complicated by the Ka
sabach-Merritt syndrome, respiratory distress due to airway compression and
high-output heart failure. This haemangioma and intravascular disseminated
coagulation, treated initially by aspirin, ticlopidine and corticosteroids
, required more invasive treatment with superselective embolisation and int
erferon alpha-2a. The clinical outcome was good.