[PHACES syndrome]

Cir Pediatr. 2010 Apr;23(2):92-4.
[Article in Spanish]

Abstract

Introduction: PHACES syndrome associates a segmental facial hemangioma with cerebral malformations, aortic branches/cranial arteries anomalies, cardiac defects, eye anomalies or ventral wall defects. The aim of this study is to analyze our experience with this syndrome.

Material and methods: Retrospective study of the cases seen at our unit in the last year.

Results: We treat 4 cases; 3 girls and 1 child. Besides the segmental hemangioma they presented: 3 vascular cerebral malformations; 2 structural cardiopathies; 2 cerebral malformations, 1 microftalmia. We did not find ventral wall defects. A case received treatment with two cycles of metilprednisolone i.v. and oral prednisone, with favourable course; two cases received initial treatment with oral prednisone continued of oral propanolol in rising pattern up to 2 mg/kg/day, Obtaining both the detention of the tumour growth and regression of the lesion, with very good tolerance. A 7-year-old patient has been treated with colouring pulse laser for her residual lesions.

Conclusions: When we see a segmental facial hemangioma we must perform a wide diagnostic study in order to discard a PHACES syndrome. Multidisciplinar approach to the patient by a wide expert's group gets an earlier diagnose and improves the outcome. Propranolol is a promising therapeutic alternative.

Publication types

  • Case Reports
  • English Abstract

MeSH terms

  • Abnormalities, Multiple* / diagnosis
  • Abnormalities, Multiple* / therapy
  • Brain / abnormalities
  • Child
  • Eye Abnormalities / diagnosis
  • Eye Abnormalities / therapy
  • Female
  • Head and Neck Neoplasms / diagnosis
  • Head and Neck Neoplasms / therapy
  • Heart Defects, Congenital / diagnosis
  • Heart Defects, Congenital / therapy
  • Hemangioma / diagnosis
  • Hemangioma / therapy
  • Humans
  • Infant
  • Intracranial Arteriovenous Malformations / diagnosis
  • Intracranial Arteriovenous Malformations / therapy
  • Male
  • Phenotype
  • Retrospective Studies
  • Syndrome