Related Experiment Videos

Occipital-parietal encephalopathy: a new name for an old syndrome

S G Pavlakis1, Y Frank, P Kalina

  • 1Department of Neurology, North Shore University Hospital, Manhasset, NY, 11030, USA.

Pediatric Neurology
|February 1, 1997
PubMed

Insights

A boy experienced severe symptoms including hypertension and seizures, which resolved with treatment. This condition, potentially a variant of reversible posterior leukoencephalopathy, may warrant a new name: occipital-parietal encephalopathy syndrome.

Area of Science:

  • Neurology
  • Pediatric Neurology
  • Neuroimaging

Background:

  • Reversible posterior leukoencephalopathy syndrome (RPLS) is a neurological condition.
  • RPLS typically affects adults and is characterized by specific brain imaging findings.

Observation:

  • A pediatric case presented with severe hypertension, seizures, lethargy, headache, and occipital blindness.
  • The patient showed significant clinical improvement following antihypertensive therapy.

Findings:

  • The clinical presentation in this child shares similarities with reported pediatric cases and adult RPLS.
  • The involvement of both gray and white matter in the observed condition suggests a broader pathological process than initially recognized in RPLS.

Implications:

  • The findings suggest that occipital-parietal encephalopathy syndrome may be a more accurate descriptor for this condition, encompassing both gray and white matter involvement.
  • Recognizing this distinct syndrome is crucial for accurate diagnosis and effective management in pediatric and potentially adult populations.
  • Further research is warranted to fully elucidate the pathophysiology and establish definitive diagnostic criteria for occipital-parietal encephalopathy syndrome.

Related Concept Videos