Abstract
Internal carotid dissection can be responsible for stroke and lead to severe neurological
and functional complications. Thus, it must be diagnosed and treated with heparin
as soon as possible. Horner syndrome is one of the most usual manifestations of internal
carotid dissection. We report the case of a patient who presented with a unilateral
non-reactive enlargement of the right pupil that did not last longer than 30 s. As
a carotid dissection was not recognized from this atypical symptomatology, magnetic
resonance angiography was performed only a few days later when Horner syndrome occurred.
It disclosed a dissection of the internal carotid artery ipsilateral from its origin.
The evolution and the duration of the pupil involvement suggest that the initial episode
of mydriasis was caused by an oculosympathetic spasm, a rare form of sympathetic dysfunction
that can be observed when the sympathetic nerve or the pericarotid plexus is irritated.
It is important to recognize this oculosympathetic spasm because it has equal value
as Horner syndrome for the diagnosis of internal carotid dissection.
Keywords
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Article info
Publication history
Published online: May 06, 2008
Accepted:
October 30,
2007
Received in revised form:
May 17,
2007
Received:
October 24,
2006
Identification
Copyright
© 2010 Elsevier Inc. Published by Elsevier Inc. All rights reserved.