Acalvaria: Case report

Ammar H. Hawasli, Thomas L. Beaumont, Timothy W. Vogel, Albert S. Woo, Jeffrey R. Leonard

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

Acalvaria is a rare congenital malformation characterized by an absence of skin and skull. The authors describe a newborn at an estimated 38 weeks gestational age who was delivered via cesarean section from a 32-year-old mother. Upon delivery, the child was noted to have a frontal encephalocele and an absence of calvaria including skull and skin overlying the brain. A thin membrane representing dura mater was overlying the cortical tissue. After multiple craniofacial operations, including repair of the encephalocele and application of cultured keratinocytes over the rostral defect, the patient demonstrated significant closure of the calvarial defect and was alive at an age of more than 17 months with near-average development.

Original languageEnglish
Pages (from-to)200-202
Number of pages3
JournalJournal of Neurosurgery: Pediatrics
Volume14
Issue number2
DOIs
StatePublished - Aug 2014

Keywords

  • Acalvaria
  • Acrania
  • Congenital malformation
  • Spina bifida

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    Hawasli, A. H., Beaumont, T. L., Vogel, T. W., Woo, A. S., & Leonard, J. R. (2014). Acalvaria: Case report. Journal of Neurosurgery: Pediatrics, 14(2), 200-202. https://doi.org/10.3171/2014.5.PEDS13688