A Giant Basal Meningoencephalocele Repair in a Neonate: A Case Report

Andrew Vogler1, Alexis Tovar2, Eugene Kim3

  • 1From the Department of Anesthesia, Indiana University School of Medicine, Indianapolis, Indiana.

A&A Practice
|July 18, 2024
PubMed

Insights

Primary encephaloceles are congenital defects causing brain protrusion. This case highlights a rare giant basal meningoencephalocele involving nasal and oral cavities, posing anesthetic challenges and risk of thecal sac rupture.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Surgical Anatomy

Background:

  • Primary encephaloceles are congenital mesodermal defects involving brain tissue protrusion through the skull.
  • These defects occur most commonly in the occipital region but can manifest anywhere on the calvarium.
  • Meningoencephaloceles, a subtype, involve herniation of both meninges and brain tissue.

Observation:

  • Basal meningoencephaloceles associated with cleft palate defects represent an extremely rare presentation.
  • This report details a case of a giant basal meningoencephalocele extending into the nasal and oral cavities.
  • The anatomical complexity presented a significant risk of thecal sac rupture.

Findings:

  • Giant basal meningoencephalocele involving the naso-oral cavities is exceptionally rare.
  • Anesthetic management for such extensive defects requires careful consideration due to potential complications.
  • The risk of thecal sac rupture is a critical factor in surgical planning.

Implications:

  • This case underscores the importance of recognizing rare congenital skull base defects.
  • Anesthetic strategies must be tailored to the unique anatomical challenges posed by giant basal meningoencephaloceles.
  • Further research into anesthetic implications for these rare conditions is warranted to improve patient outcomes.