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Diagnostic brain MRI findings in primary progressive multiple sclerosis

Department of Clinical Neurological Sciences, London Health Sciences Centre-UC, 339 Windermere Road, London, Ontario N6A 5A5, Canada

D Lee

Department of Neuro-Radiology, London Health Sciences Centre-UC, 339 Windermere Road, London, Ontario N6A 6A6, Canada

G P A Rice

Department of Clinical Neurological Sciences, London Health Sciences Centre-UC, 339 Windermere Road, London, Ontario N6A 5A5, Canada

G C Ebers

Department of Clinical Neurological Sciences, London Health Sciences Centre-UC, 339 Windermere Road, London, Ontario N6A 5A5, Canada

The clinical course of multiple sclerosis can be classified as relapsing from onset (relapsing-remitting), or progressive from onset (primary progressive -PPMS). These clinical phenotypes have been based on historical and clinical observations. It has been reported that PPMS patients tend to have quantitatively less MRI activity and disease burden. We evaluated the sensitivity and diagnostic value of conventional brain MRI scan in 143 PPMS patients. Brain MRIs were blindly evaluated to determine if they satisfied Paty and/or Fazekas diagnostic criteria. Patient were divided into those with typical atypical or normal scans. They satisfied brain MRI criteria in 92% cases. Findings included: 131 typical four atypical, and eight normal scans. All 12 non-typical scans' subject had spinal onset; spinal MRI scans were positive in four of seven cases. Sex, age of onset, site and number of symptoms involved at onset among those groups were not significantly different but accumulation of disability had a tendency to be slower in these few individuals with normal or atypical head MRI's. Although there may be quantitative differences in lesion activity/burden, MRI scanning in PPMS unexpectedly has diagnostic sensitivity very similar to that seen in RRMS. A normal brain MRI is unusual in PPMS patients.

Key Words: primary progressive-multiple sclerosis • magnetic resonance imaging • diagnostic criteria

Multiple Sclerosis, Vol. 6, No. 2, 81-85 (2000)
DOI: 10.1177/135245850000600205


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