Vol 49, No 1 (2015)

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Red ear syndrome – Case report and review of literature

Jedrzej Flicinski1, Jadwiga Wigowska-Sowinska1, Anna Winczewska-Wiktor1, Barbara Steinborn1
DOI: 10.1016/j.pjnns.2015.01.004
Neurol Neurochir Pol 2015;49(1):74-77.

Abstract

Red 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.

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Neurologia i Neurochirurgia Polska