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Idiopathic red ear syndrome: A rare case report
Red ear syndrome (RES) is a very rare disorder that is characterized by a unilateral or bilateral attack of paroxysmal burning sensation and reddening of the external ear. The duration of symptoms ranges from a few seconds to hours. It can occur spontaneously or be triggered by rubbing of the ear, h...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917311/ https://www.ncbi.nlm.nih.gov/pubmed/35310317 http://dx.doi.org/10.1002/ccr3.5564 |
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author | Sigdel, Brihaspati Pokhrel, Amrit |
author_facet | Sigdel, Brihaspati Pokhrel, Amrit |
author_sort | Sigdel, Brihaspati |
collection | PubMed |
description | Red ear syndrome (RES) is a very rare disorder that is characterized by a unilateral or bilateral attack of paroxysmal burning sensation and reddening of the external ear. The duration of symptoms ranges from a few seconds to hours. It can occur spontaneously or be triggered by rubbing of the ear, heat or cold stimulation, brushing of hair, and neck movement. Diagnosis and treatment of this condition are challenging. The pathophysiology of RES is still unclear and hypotheses involving peripheral or central nervous system mechanisms have been proposed. RES is regarded as refractory to medical treatments, although some migraine preventative treatments have shown moderate benefit mainly in patients with migraine‐related attacks. We report a case with Idiopathic RES who presented with paroxysmal redness of the bilateral pinnae partially benefitted by medical treatment. |
format | Online Article Text |
id | pubmed-8917311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89173112022-03-18 Idiopathic red ear syndrome: A rare case report Sigdel, Brihaspati Pokhrel, Amrit Clin Case Rep Case Reports Red ear syndrome (RES) is a very rare disorder that is characterized by a unilateral or bilateral attack of paroxysmal burning sensation and reddening of the external ear. The duration of symptoms ranges from a few seconds to hours. It can occur spontaneously or be triggered by rubbing of the ear, heat or cold stimulation, brushing of hair, and neck movement. Diagnosis and treatment of this condition are challenging. The pathophysiology of RES is still unclear and hypotheses involving peripheral or central nervous system mechanisms have been proposed. RES is regarded as refractory to medical treatments, although some migraine preventative treatments have shown moderate benefit mainly in patients with migraine‐related attacks. We report a case with Idiopathic RES who presented with paroxysmal redness of the bilateral pinnae partially benefitted by medical treatment. John Wiley and Sons Inc. 2022-03-11 /pmc/articles/PMC8917311/ /pubmed/35310317 http://dx.doi.org/10.1002/ccr3.5564 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Sigdel, Brihaspati Pokhrel, Amrit Idiopathic red ear syndrome: A rare case report |
title | Idiopathic red ear syndrome: A rare case report |
title_full | Idiopathic red ear syndrome: A rare case report |
title_fullStr | Idiopathic red ear syndrome: A rare case report |
title_full_unstemmed | Idiopathic red ear syndrome: A rare case report |
title_short | Idiopathic red ear syndrome: A rare case report |
title_sort | idiopathic red ear syndrome: a rare case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8917311/ https://www.ncbi.nlm.nih.gov/pubmed/35310317 http://dx.doi.org/10.1002/ccr3.5564 |
work_keys_str_mv | AT sigdelbrihaspati idiopathicredearsyndromeararecasereport AT pokhrelamrit idiopathicredearsyndromeararecasereport |