Bilateral facial capillary malformation associated with eye and brain abnormalities

Arch Dermatol. 2006 Aug;142(8):994-8. doi: 10.1001/archderm.142.8.994.

Abstract

Objective: To establish whether the prognosis of bilateral facial capillary malformation (BFCM) is worse compared with that of unilateral facial port-wine stain.

Design: Retrospective study.

Setting: Paediatric Dermatology Department, Great Ormond Street Hospital for Children NHS Trust, a tertiary referral center for vascular anomalies.

Patients: A cohort of 350 children who presented with facial CM was seen between January 1, 1994, and June 30, 2004. Twenty-seven children with BFCM were identified. A control group of 27 children with unilateral CM was randomly selected from the total cohort.

Main outcome measures: Demographic, clinical, and radiographic characteristics were recorded and compared between the 2 groups: age at presentation, sex, distribution, extension, extrafacial lesions, glaucoma, ipsilateral leptomeningeal angiomatosis, and epilepsy. The recorded information was collected from the database of the Paediatric Dermatology Department, the hospital records, and the patients' photographs.

Results: Compared with the 27 children with unilateral facial CM, the 27 with BFCM showed a higher frequency of association with extrafacial lesions (17 [63%] vs 6 [22%]), glaucoma (21 [78%] vs 2 [7%]), and ipsilateral leptomeningeal angiomatosis (14 [52%] vs 2 [7%]). All patients who had BFCM with bilateral and complete involvement of the ophthalmic area had ipsilateral leptomeningeal angiomatosis.

Conclusion: Patients with BFCM must be considered as a group with a worse prognosis compared with patients with unilateral facial CM.

MeSH terms

  • Abnormalities, Multiple
  • Adolescent
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Cohort Studies
  • England / epidemiology
  • Epilepsy / complications*
  • Facial Dermatoses / complications
  • Facial Dermatoses / epidemiology*
  • Facial Dermatoses / pathology
  • Female
  • Glaucoma / complications*
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Port-Wine Stain / complications
  • Port-Wine Stain / epidemiology*
  • Port-Wine Stain / pathology
  • Retrospective Studies
  • Severity of Illness Index