Literature DB >> 12223030

Impairment of the peripheral nervous system in Creutzfeldt-Jakob disease.

Maria Niewiadomska1, Jerzy Kulczycki, Danuta Wochnik-Dyjas, Grazyna M Szpak, Maria Rakowicz, Wanda Łojkowska, Krystyna Niedzielska, Ewa Inglot, Malgorzata Wieclawska, Czeslaw Glazowski, Eugenia Tarnowska-Dziduszko.   

Abstract

BACKGROUND: The clinical manifestations of Creutzfeldt-Jakob disease (CJD) primarily reflect involvement of the central nervous system. The coexistence of CJD with peripheral nervous system involvement has also been reported.
OBJECTIVE: To analyze peripheral neuron electrophysiologic changes and to compare these data with neuropathologic features of spinal motor neurons in patients with definite CJD. DESIGN AND PATIENTS: Electrophysiologic examinations were performed on 16 patients with sporadic CJD. The diagnosis was confirmed by neuropathologic examinations (15 patients) or by intravital detection of the 14-3-3 protein in the cerebrospinal fluid (1 patient). The spinal cord was neuropathologically examined in 8 patients.
SETTING: Department of Clinical Neurophysiology, I Neurological Department, Institute of Psychiatry and Neurology, Warsaw, Poland. MAIN OUTCOME MEASURES: Electromyography, compound muscle and sensory nerve action potentials, distal latencies, F waves, peripheral motor and sensory conduction velocity, and spinal motor neuron numbers and morphologic characteristics.
RESULTS: All patients had signs of central nervous system damage typical of sporadic CJD. Only 3 patients had clinical signs of peripheral nervous system involvement. Electrophysiologic examinations confirmed peripheral nervous system damage in these patients and revealed preclinical peripheral nervous system impairment in 11 more patients. In 1 patient, electrophysiologic examination revealed features of motor neuron disease; in 9, axonal disease; and in 4, axonal-demyelinating neuropathy. Neuropathologic examination results confirmed severe loss of spinal motor neurons in 1 patient with motor neuron disease and revealed the features of motor neuron chronic disease in 4. In 2 of them, electrophysiologic data were normal.
CONCLUSION: In sporadic cases of CJD, peripheral nervous system impairment should be considered to be an integral component of disease.

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Year:  2002        PMID: 12223030     DOI: 10.1001/archneur.59.9.1430

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  9 in total

1.  Severe and rapidly evolving peripheral neuropathy revealing sporadic Creutzfeldt-Jakob disease.

Authors:  Hélène Zéphir; Tanya Stojkovic; Jérome de Seze; Claude-Alain Maurage; Katell Peoc'h; Stéphane Haïk; Patrick Vermersch
Journal:  J Neurol       Date:  2009-02-07       Impact factor: 4.849

2.  Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease.

Authors:  C Ishida; S Okino; T Kitamoto; M Yamada
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-03       Impact factor: 10.154

3.  Isolated spasticity in sporadic Creutzfeldt-Jakob disease.

Authors:  Milena Marek; Thomas Klockgether; Horst Urbach; Inga Zerr; Hans Kretzschmar; Sebastian Paus
Journal:  J Neurol       Date:  2012-11-16       Impact factor: 4.849

4.  Peripheral nervous system hyperexcitability in VV2 sporadic Creutzfeldt-Jakob disease.

Authors:  Charlene J Ong; Muhammad Al-Lozi; Patrick J Cimino; Robert Bucelli
Journal:  Neurol Clin Pract       Date:  2015-08

5.  Unusual presentations in patients with E200K familial Creutzfeldt-Jakob disease.

Authors:  O S Cohen; I Kimiagar; A D Korczyn; Z Nitsan; S Appel; C Hoffmann; H Rosenmann; E Kahana; J Chapman
Journal:  Eur J Neurol       Date:  2016-01-25       Impact factor: 6.089

6.  Creutzfeldt-Jakob disease with unusual presentation of peripheral neuropathy and ophthalmoplegia.

Authors:  Mais Arwani; Abhishek Purohit; Abdullah Haddad; Sandeep Rana
Journal:  Avicenna J Med       Date:  2018 Oct-Dec

7.  Prion type 2 selection in sporadic Creutzfeldt-Jakob disease affecting peripheral ganglia.

Authors:  Anna Hofmann; Arne Wrede; Wiebke M Jürgens-Wemheuer; Walter J Schulz-Schaeffer
Journal:  Acta Neuropathol Commun       Date:  2021-11-24       Impact factor: 7.801

8.  A patient with Creutzfeldt-Jakob disease presenting with amyotrophy: a case report.

Authors:  Peter K Panegyres; Elizabeth Armari; Richard Shelly
Journal:  J Med Case Rep       Date:  2013-08-23

9.  Genetic Creutzfeldt-Jakob disease mimicking chronic inflammatory demyelinating polyneuropathy.

Authors:  Dorien Weckhuysen; Maarten Schrooten; Philippe Demaerel; Christine Van Broeckhoven; Thomas Tousseyn; Gabor G Kovacs; Philip Van Damme
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2015-10-29
  9 in total

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