Encephalocystocele - uncommon diagnosis in prenatal medicine

Fetal Diagn Ther. 2012;32(4):295-8. doi: 10.1159/000341569. Epub 2012 Oct 24.

Abstract

Encephalocystocele is a developmental malformation characterized by brain herniation accompanied with extracranial cystic protrusion of the ventricular system. This nosological unit is often overlooked and insufficiently classified merely as encephalocele. Herein, two exceptionally clear cases of the parieto-occipital cranioschisis with encephalocystocele and congenital hydrocephalus of the lateral ventricles are documented with 2-dimensional/3-dimensional sonographic images and the corresponding MRI findings. In both cases, prenatal diagnosis was confirmed by autopsy.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abortion, Eugenic
  • Adult
  • Cesarean Section
  • Cystocele / diagnosis*
  • Cystocele / embryology
  • Cystocele / pathology
  • Cystocele / physiopathology
  • Encephalocele / diagnosis*
  • Encephalocele / embryology
  • Encephalocele / pathology
  • Encephalocele / physiopathology
  • Fatal Outcome
  • Female
  • Humans
  • Infant, Newborn
  • Magnetic Resonance Imaging
  • Meningocele / diagnosis*
  • Meningocele / embryology
  • Meningocele / pathology
  • Meningocele / physiopathology
  • Pregnancy
  • Pregnancy Trimester, Second
  • Prenatal Diagnosis
  • Term Birth