PHACE syndrome--clinical features, aetiology and management

Acta Paediatr. 2016 Feb;105(2):145-53. doi: 10.1111/apa.13242. Epub 2015 Nov 27.

Abstract

PHACE syndrome comprises a spectrum of anomalies including posterior fossa malformations, haemangioma, arterial anomalies, cardiac defects and eye anomalies. PHACE should be considered in any patient with a large facial segmental infantile haemangioma (IH), and multidisciplinary management is crucial. Low-dose propranolol is effectively for the treatment of IH associated with PHACE syndrome. Recent evidence suggests IH is comprised of mesoderm-derived haemogenic endothelium.

Conclusion: The embryonic developmental anomaly nature of IH provides an insight into the origin of PHACE syndrome.

Keywords: Aetiology; Infantile haemangioma; PHACE syndrome; Renin-angiotensin system; β-blockers.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adrenergic beta-Antagonists / therapeutic use
  • Aortic Coarctation* / drug therapy
  • Aortic Coarctation* / embryology
  • Eye Abnormalities* / drug therapy
  • Eye Abnormalities* / embryology
  • Female
  • Humans
  • Infant
  • Neurocutaneous Syndromes* / drug therapy
  • Neurocutaneous Syndromes* / embryology

Substances

  • Adrenergic beta-Antagonists

Supplementary concepts

  • PHACE association