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Transethmoidal encephalocele endoscopically treated in a newborn: a case report.

Cristiano ParisiRoberto SaettiLiliana Laura PetittoMariangela NovelloLorenzo VolpinOriela Rustemi
Published in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2020)
Congenital encephalocele is a very rare entity, with herniation of normal brain or gliotic tissue through a defect in the skull. The objective is to present a newborn child diagnosed with transethmoidal encephaloceles at birth. She developed respiratory problems, feeding difficulties, and failure to thrive since the first days of life and so required early surgery at her 33th day of life, through an endoscopic nasal approach. Technical difficulties encountered, complications, and management are discussed. To the best of our knowledge, this is the first report of endoscopic treatment of transethmoidal encephalocele in a newborn. Further studies are needed to understand the best way to repair the dural defect in this rare condition.
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