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Subacute sclerosing panencephalitis presenting with hemiparesis in childhood: case report

Hamit Ozyürek1, Aydan Değerliyurt, Guzide Turanli

  • 1Department of Pediatric Neurology, Hacettepe University Faculty of Medicine, Ankara, Turkey. hozyurekibu@hotmail.com

Insights

Subacute sclerosing panencephalitis (SSPE) is a fatal neurological disease. Early diagnosis is crucial, as this case highlights SSPE presenting with focal neurological signs in an infant.

Area of Science:

  • Neurology
  • Pediatrics
  • Infectious Diseases

Background:

  • Subacute sclerosing panencephalitis (SSPE) is a rare, chronic, and fatal central nervous system disease.
  • It is a late complication of measles virus infection, typically occurring years after the initial illness.

Observation:

  • A 14-month-old girl presented with left-sided hemiparesis.
  • During hospitalization, she developed focal and generalized seizures.
  • Electroencephalogram (EEG) showed periodic lateralized discharges with polyspike and high-voltage slow waves in the left hemisphere.

Findings:

  • Clinical presentation, EEG findings, and positive measles serology in cerebrospinal fluid confirmed the diagnosis of SSPE.
  • The patient's presentation with focal neurological deficits was atypical for SSPE, which commonly presents with psychointellectual disturbances.

Implications:

  • This case underscores the importance of considering SSPE in the differential diagnosis of focal neurological signs in infants.
  • Early recognition and diagnosis of SSPE are critical for potential management strategies, despite its generally poor prognosis.

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