From Diagnosis to Discharge: Case of a Giant Occipital Encephalocele

Rhianon L Brock1, Amy Jnah2

  • 1Department of Advanced Practice Nursing Practice & Education, East Carolina University, College of Nursing, Greenville, NC, USA brockr15@students.ecu.edu.

Neonatal Network : NN
|August 15, 2025
PubMed

Insights

Giant occipital encephalocele is a rare congenital brain malformation where brain tissue and CSF protrude through a skull defect. This case study details a neonate

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Pediatric Surgery

Background:

  • Occipital encephalocele is a rare congenital brain malformation.
  • It involves protrusion of brain tissue and cerebrospinal fluid (CSF) through a skull defect.
  • Giant occipital encephalocele is defined by its large size relative to the head circumference.

Purpose of the Study:

  • To present a case study of a neonate with giant occipital encephalocele.
  • To discuss the risk factors, pathophysiology, clinical manifestations, diagnosis, and management of this condition.
  • To highlight the importance of family-centered care in managing such cases.

Main Methods:

  • Case report presentation.
  • Literature review for risk factors, pathophysiology, and clinical aspects.
  • Discussion of diagnostic and management strategies.
  • Exploration of psychosocial implications for families and care providers.

Main Results:

  • Detailed account of a neonate diagnosed with giant occipital encephalocele.
  • Comprehensive overview of the disease spectrum, from etiology to treatment.
  • Emphasis on the multidisciplinary approach required for optimal outcomes.
  • Recognition of the significant impact on the family unit and healthcare team.

Conclusions:

  • Giant occipital encephalocele requires a thorough understanding of its complex nature.
  • Early diagnosis and appropriate management are crucial for affected neonates.
  • Integrated family support is essential for holistic patient care and successful outcomes.