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MRI follow-up in a case of clinically diagnosed Creutzfeld-Jakob disease

A Hutzelmann1, J Biederer

  • 1Department of Radiology, Christian-Albrechts-Universität zu Kiel, Arnold Heller Strasse 9, D-24105 Kiel, Germany.

European Radiology
|May 2, 1998
PubMed

Insights

This case study highlights a 75-year-old woman diagnosed with Creutzfeldt-Jakob disease (CJD). Cranial MRI revealed progressive brain atrophy and specific signal changes, supporting the diagnosis without biopsy.

Area of Science:

  • Neurology
  • Radiology

Background:

  • Creutzfeldt-Jakob disease (CJD) is a rare, fatal neurodegenerative disorder.
  • Diagnosis often relies on clinical presentation and definitive neuropathological confirmation, typically post-mortem or via biopsy.

Observation:

  • A 75-year-old female presented with symptoms suggestive of CJD.
  • Brain biopsy was declined, necessitating alternative diagnostic methods.
  • Serial cranial Magnetic Resonance Imaging (MRI) examinations were performed over four months.

Findings:

  • MRI revealed progressive cortical atrophy.
  • T2-weighted imaging showed bilateral increased signal intensity in the caudate nuclei and putamina.
  • These imaging findings indicated the development of spongiform degeneration, characteristic of CJD.

Implications:

  • The observed clinical course and MRI findings strongly correlated with neuropathologically confirmed CJD cases.
  • This case suggests that cranial MRI is a valuable non-invasive tool for the clinical diagnosis of CJD.
  • Routine use of MRI could aid in earlier and more accessible diagnosis of CJD.

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