Monobloc and midface distraction osteogenesis in pediatric patients with severe syndromal craniosynostosis

T R Meling1, S Tveten, B J Due-Tonnessen

  • 1Department of Neurosurgery, National Hospital, Ullevaal Hospital, Oslo, Norway. torsteinrmeling@mailicity.com

Pediatric Neurosurgery
|November 9, 2000
PubMed

Insights

Distraction osteogenesis safely advanced midfaces in children with syndromal craniosynostosis, resolving ocular dislocations and respiratory issues. This technique enables significant skeletal advancements for complex craniofacial conditions.

Area of Science:

  • Craniofacial Surgery
  • Pediatric Plastic Surgery
  • Orthognathic Surgery

Background:

  • Syndromal craniosynostosis, including Pfeiffer syndrome type II and Crouzon syndrome, often necessitates urgent surgical intervention.
  • Severe cases present with life-threatening complications like ocular dislocations and upper respiratory obstruction.

Observation:

  • Two pediatric patients with severe syndromal craniosynostosis required immediate midface advancement.
  • One patient had Pfeiffer syndrome type II with recurrent ocular dislocations; the other had Crouzon syndrome with severe respiratory obstruction.

Findings:

  • Distraction osteogenesis was employed for gradual midface or monobloc advancements.
  • A 25 mm maxillary distraction in the Pfeiffer patient ceased ocular dislocations.
  • A 23 mm monobloc advancement in the Crouzon patient resolved nocturnal arterial desaturations.
  • No major postoperative complications were observed in either case.

Implications:

  • Distraction osteogenesis is a versatile and safe method for achieving substantial skeletal advancements in pediatric craniofacial surgery.
  • This technique offers a viable solution for managing severe syndromal craniosynostosis complications.

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