Extreme Hypertrophy of Peripheral Neuronal Structures in CIDP – a Case Study
Authors:
J. Michalik 1; E. Kurča 1; M. Hladká 2; B. Hofericová 1; V. Nosáľ 1; M. Grofik 1; E. Kantorová 1; M. Adámková 1
Authors‘ workplace:
JLF UK a UN Martin
Neurologická klinika
1; JLF UK a UN Martin
Rádiologická klinika
2
Published in:
Cesk Slov Neurol N 2011; 74/107(1): 72-75
Category:
Case Report
Overview
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is an autoimmune peripheral nerve disease characterized by flaccid quadriparesis with loss of sensitivity and possible damage to cranial nerves. The diagnosis of CIDP nay involve electromyography (EMG), cerebrospinal fluid analysis, nerve biopsy, magnetic resonance imaging (MRI) of peripheral nerves and the clinical response to immunosuppression and/or immunomodulation. MRI facilitates early detection of nerve hypertrophy. In our case report we present an unusual CIDP with extreme hypertrophy of the peripheral nerves and spinal roots.
Key words:
chronic inflammatory demyelinating polyradiculoneuropathy – hypertrophy – magnetic resonance imaging
Sources
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Labels
Paediatric neurology Neurosurgery NeurologyArticle was published in
Czech and Slovak Neurology and Neurosurgery
2011 Issue 1
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