An initial MRI picture of limbic encephalitis in subacute sclerosing panencephalitis

Sébastien Lebon1, Philippe Maeder, Malin Maeder-Ingvar

  • 1Unité de Neurologie et de Neurorehabilitation Pédiatrique, Département Médico-Chirurgical de Pédiatrie, CHUV, Lausanne, Switzerland. Sebastien.Lebon@chuv.ch

Abstract

Insights

Subacute sclerosing panencephalitis (SSPE), a rare measles complication, presented unusually in a teen with limbic encephalitis-like brain MRI findings. This case highlights atypical presentations of SSPE, emphasizing the need for broader diagnostic considerations.

Area of Science:

  • Neurology
  • Virology
  • Radiology

Background:

  • Subacute sclerosing panencephalitis (SSPE) is a rare, severe neurological complication of measles infection.
  • Typical SSPE features include cognitive decline, myoclonia, specific EEG patterns, and white matter changes on MRI.
  • Early-stage SSPE may present with normal or subtle imaging findings.

Observation:

  • A previously healthy 13-year-old girl presented with unilateral myoclonia and cognitive decline.
  • Initial brain MRI revealed hippocampal swelling, mimicking limbic encephalitis.
  • Cerebrospinal fluid (CSF) showed positive measles antibodies, and EEG displayed slow periodic complexes.

Findings:

  • The patient's presentation with limbic encephalitis-like imaging is an unusual radiological manifestation of SSPE.
  • Positive measles antibodies in CSF confirmed a link to measles virus.
  • EEG findings were consistent with SSPE, despite the atypical MRI.

Implications:

  • This case expands the spectrum of radiological presentations for SSPE.
  • It underscores the importance of considering SSPE even with atypical imaging, particularly in the presence of compatible clinical and laboratory findings.
  • Further research into the virus-host interaction within the limbic system in SSPE is warranted.

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