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Neurol Neurochir Pol · Jan 2015
Review Case ReportsRed ear syndrome - case report and review of literature.
- Jedrzej Flicinski, Jadwiga Wigowska-Sowinska, Anna Winczewska-Wiktor, and Barbara Steinborn.
- Chair and Department of Developmental Neurology, Poznan University of Medical Sciences, Poznan, Poland. Electronic address: flicinski@ump.edu.pl.
- Neurol Neurochir Pol. 2015 Jan 1;49(1):74-7.
AbstractRed ear syndrome is characterized by: paroxysmal, unilateral, recurrent pain, redness and discomfort of the ear lobe accompanied by a burning sensation. The duration and frequency of red ear syndrome attacks is very various and the episodes, usually occur spontaneously. The pathophysiology is still unknown and also there are no medications with approved efficacy. The goal of this brief report is to present a 11-year old girls whose symptoms of red ear syndrome preceded migraine without aura and the signs of redness of the ear occurred in clusters. The occurrence of symptoms of our case may have confirmed the observation that red ear syndrome is associated with primary headaches particularly migraine and cluster headaches. The literature on this case report of pediatric idiopathic red ear syndrome has been reviewed.Copyright © 2015 Polish Neurological Society. Published by Elsevier Urban & Partner Sp. z o.o. All rights reserved.
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