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Neuropathological findings in a child with slit ventricle syndrome

Marc R Del Bigio1

  • 1Department of Pathology, Health Sciences Centre, and Manitoba Institute of Child Health, Winnipeg, Canada. delbigi@cc.umanitoba.ca

Pediatric Neurosurgery
|August 21, 2002
PubMed

Insights

Slit ventricle syndrome in shunted hydrocephalic children is poorly understood. Histopathology reveals glial adhesions and shunt obstruction, but periventricular astrogliosis may not be the primary cause.

Area of Science:

  • Pediatric Neurology
  • Neuroscience
  • Histopathology

Background:

  • Shunt placement is common for hydrocephalus in children.
  • Slit ventricle syndrome (SVS) is a rare complication of shunted hydrocephalus.
  • The histopathological features of SVS are not well-documented.

Observation:

  • A 10-year-old girl with a history of infantile meningitis and shunt placement developed SVS.
  • She experienced headaches, respiratory arrest, and was found to have very small ventricles on CT scan.
  • Post-mortem examination revealed small ventricles with glial adhesions, aqueductal obstruction, and a completely blocked shunt catheter.

Findings:

  • Autopsy confirmed SVS with significant neuropathological findings.
  • Periventricular white matter showed reactive astroglia, but this was not more severe than in other hydrocephalic children with shunt failure.
  • Glial adhesions within the small ventricles were noted.

Implications:

  • Periventricular astrogliosis may not be the sole or primary determinant of SVS.
  • This case highlights the complex histopathological changes in SVS.
  • Further research is needed to fully understand the pathogenesis of SVS.

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