Movement Disorders (revue)

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Anhidrosis in multiple system atrophy: A preganglionic sudomotor dysfunction?

Identifieur interne : 002A06 ( Main/Exploration ); précédent : 002A05; suivant : 002A07

Anhidrosis in multiple system atrophy: A preganglionic sudomotor dysfunction?

Auteurs : Vincenzo Donadio [Italie] ; Maria Nolano [Italie] ; Mikael Elam [Suède] ; Pasquale Montagna [Italie] ; Vincenzo Provitera [Italie] ; Enrico Bugiardini [Italie] ; Agostino Baruzzi [Italie] ; Lucio Santoro [Italie] ; Rocco Liguori [Italie]

Source :

RBID : ISTEX:4023D2E6105372B0E629EAAAFD09E48E53C5B891

Descripteurs français

English descriptors

Abstract

Anhidrosis occurs in the majority of multiple system atrophy (MSA) patients but the underlying site of lesion is not well established. We describe three patients with long‐standing MSA and anhidrosis diagnosed on the basis of a thermoregulatory sweating test. In biopsies of anhidrotic skin, immunofluorescence analysis disclosed a well preserved postganglionic sudomotor innervation in all three patients supporting the hypothesis of a preganglionic nerve fiber lesion underlying their anhidrosis. Postganglionic sudomotor fiber integrity was also confirmed by normal electrodermal responses in one patient, whereas such responses and microneurographically detectable skin sympathetic nerve activity were absent in the other two MSA patients, suggesting a functional inactivity of structurally intact postganglionic sympathetic skin fibers. © 2008 Movement Disorder Society.

Url:
DOI: 10.1002/mds.21972


Affiliations:


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Le document en format XML

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<term>Biopsy</term>
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<div type="abstract" xml:lang="en">Anhidrosis occurs in the majority of multiple system atrophy (MSA) patients but the underlying site of lesion is not well established. We describe three patients with long‐standing MSA and anhidrosis diagnosed on the basis of a thermoregulatory sweating test. In biopsies of anhidrotic skin, immunofluorescence analysis disclosed a well preserved postganglionic sudomotor innervation in all three patients supporting the hypothesis of a preganglionic nerve fiber lesion underlying their anhidrosis. Postganglionic sudomotor fiber integrity was also confirmed by normal electrodermal responses in one patient, whereas such responses and microneurographically detectable skin sympathetic nerve activity were absent in the other two MSA patients, suggesting a functional inactivity of structurally intact postganglionic sympathetic skin fibers. © 2008 Movement Disorder Society.</div>
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