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Chronic inflammatory demyelinating polyneuropathy presenting with headache and papilledema.

Chronic inflammatory demyelinating polyneuropathy presenting with headache and papilledema.
Chronic inflammatory demyelinating polyneuropathy presenting with headache and papilledema.
Chronic inflammatory demyelinating polyneuropathy is a disorder typified clinically by motor and sensory neuropathy of at least 2 months' duration and pathologically by multifocal inflammatory demyelination. Its usual presentation is with features reflecting the polyneuropathy, namely limb weakness with hyporeflexia or areflexia and sensory symptoms of glove and stocking distribution. In this report, we detail the course of a 53-year-old man who presented to our neurological service with a severe headache in association with papilledema. The initial diagnosis considered was of possible primary intracranial pathology. Two months later, he developed limb weakness and sensory symptoms typical of chronic inflammatory demyelinating polyneuropathy. His headache, papilledema, and limb symptoms responded to oral corticosteroid therapy, the standard treatment for this type of neuropathy. We hypothesize that his headache and papilledema were due to the elevated cerebrospinal fluid protein level as a result of the polyneuropathy. To our knowledge, this is the first report of headache being a prominent and early symptom of this disorder.
1526-4610
299-300
Morrison, K.E.
f00890f0-2fde-4dbd-a73b-7422e1b0ede8
Davies, P.T.
dde027dd-c2ce-4e17-afbb-90012372f597
Morrison, K.E.
f00890f0-2fde-4dbd-a73b-7422e1b0ede8
Davies, P.T.
dde027dd-c2ce-4e17-afbb-90012372f597

Morrison, K.E. and Davies, P.T. (1999) Chronic inflammatory demyelinating polyneuropathy presenting with headache and papilledema. Headache, 39 (4), 299-300. (doi:10.1046/j.1526-4610.1999.3904299.x). (PMID:15613228)

Record type: Article

Abstract

Chronic inflammatory demyelinating polyneuropathy is a disorder typified clinically by motor and sensory neuropathy of at least 2 months' duration and pathologically by multifocal inflammatory demyelination. Its usual presentation is with features reflecting the polyneuropathy, namely limb weakness with hyporeflexia or areflexia and sensory symptoms of glove and stocking distribution. In this report, we detail the course of a 53-year-old man who presented to our neurological service with a severe headache in association with papilledema. The initial diagnosis considered was of possible primary intracranial pathology. Two months later, he developed limb weakness and sensory symptoms typical of chronic inflammatory demyelinating polyneuropathy. His headache, papilledema, and limb symptoms responded to oral corticosteroid therapy, the standard treatment for this type of neuropathy. We hypothesize that his headache and papilledema were due to the elevated cerebrospinal fluid protein level as a result of the polyneuropathy. To our knowledge, this is the first report of headache being a prominent and early symptom of this disorder.

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Published date: April 1999
Organisations: Medical Education

Identifiers

Local EPrints ID: 399548
URI: http://eprints.soton.ac.uk/id/eprint/399548
ISSN: 1526-4610
PURE UUID: 754e1ddb-5fb9-4fd8-a064-a839335e78c2
ORCID for K.E. Morrison: ORCID iD orcid.org/0000-0003-0216-5717

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Date deposited: 18 Aug 2016 12:47
Last modified: 15 Mar 2024 01:55

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Contributors

Author: K.E. Morrison ORCID iD
Author: P.T. Davies

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