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Volume 112, Issue 3, Pages 209-212 (April 2010)


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Isolated degeneration of the posterior column as a distinct entity—A clinical and electrophysiologic follow-up study

O. KastrupCorresponding Author Informationemail address, D. Timman, H.C. Diener

Received 4 May 2009; received in revised form 21 August 2009; accepted 18 November 2009.

Abstract 

Objective

The aim of the study was to better describe the long term clinical course and electrophysiologic and radiologic findings in isolated degeneration of the posterior column.

Methods

Four patients with the presenting symptoms of a progressive tabetic ataxia were followed up clinically and electrophysiologically over up to 15 years between 1997 and 2008. They received standardized neurological examinations, electrophysiologic testing with SEP, MEP, NCV, EMG, autonomic testing and cardiac evaluation, head and spine MRI, laboratory evaluation including CSF analysis.

Results

Progressive gait ataxia due to pallhypasthesia and loss of position sense with areflexia remained the only symptoms. Pes cavus deformity was a notable clinical feature in all cases. There was no involvement of other systems and all patients remained fully ambulatory. There was no cardiac involvement. Electrophysiology was characterized by absent cortical tibial SEP with normal lumbar complexes and normal nerve conduction studies and transcortical magnetic stimulation as well as sympathetic skin response. MRI of the cord was normal. Laboratory analysis and CSF were unrevealing.

Conclusion

Isolated degeneration of the posterior column is a rare condition with a clinically benign course without progression involving other systems and characteristic electrophysiologic findings (isolated loss of cortical tibial-SEP with normal lumbar leads). Pes cavus deformity seems to be an unusual but typical clinical feature. The etiology is most likely a sporadic degenerative disease of the cord.

Department of Neurology, University of Essen, Hufelandstr. 55, 45122 Essen, Germany

Corresponding Author InformationCorresponding author. Tel.: +49 201 7232463; fax: +49 201 7235901.

PII: S0303-8467(09)00309-6

doi:10.1016/j.clineuro.2009.11.012


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