Case report: an atypical presentation of Eagle syndrome
Identifieur interne : 001F23 ( Pmc/Curation ); précédent : 001F22; suivant : 001F24Case report: an atypical presentation of Eagle syndrome
Auteurs : Edward Gallaway [Royaume-Uni] ; Sherif Bayoumi [Royaume-Uni] ; Douglas Hammond [Royaume-Uni] ; Moorthy Halsnad [Royaume-Uni]Source :
- Journal of Surgical Case Reports [ 2042-8812 ] ; 2017.
Abstract
Elongation of the styloid process occurs in 4–7% of individuals. In the majority this elongation is asymptomatic. Presence of oropharyngeal pain and dysphagia with such elongation is known as Eagle syndrome. The aetiology of Eagle syndrome is believed to be a reactive osseus hyperplasia of the styloid process in response to pharyngeal trauma or surgical intervention, such as tonsillectomy. We present a case of a 72-year-old lady with a twelve month history of left sided oropharyngeal pain and worsening dysphagia, presenting with a long, slender, bony intraoral projection found to be an elongated styloid process. She previously underwent tonsillectomy and radiotherapy on the left side for a tonsillar carcinoma. Surgical reduction of the elongated styloid process via intraoral approach led to immediate post-operative pain relief and normal swallowing. We conclude that this atypical presentation of Eagle syndrome was caused by the patient's prior treatment for tonsillar carcinoma.
Url:
DOI: 10.1093/jscr/rjx152
PubMed: 28852461
PubMed Central: 5570094
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In the majority this elongation is asymptomatic. Presence of oropharyngeal pain and dysphagia with such elongation is known as Eagle syndrome. The aetiology of Eagle syndrome is believed to be a reactive osseus hyperplasia of the styloid process in response to pharyngeal trauma or surgical intervention, such as tonsillectomy. We present a case of a 72-year-old lady with a twelve month history of left sided oropharyngeal pain and worsening dysphagia, presenting with a long, slender, bony intraoral projection found to be an elongated styloid process. She previously underwent tonsillectomy and radiotherapy on the left side for a tonsillar carcinoma. Surgical reduction of the elongated styloid process via intraoral approach led to immediate post-operative pain relief and normal swallowing. We conclude that this atypical presentation of Eagle syndrome was caused by the patient's prior treatment for tonsillar carcinoma.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Kaufman, Sm" uniqKey="Kaufman S">SM Kaufman</name></author><author><name sortKey="Elzay, Rp" uniqKey="Elzay R">RP Elzay</name></author><author><name sortKey="Irish, Ef" uniqKey="Irish E">EF Irish</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Moffat, Da" uniqKey="Moffat D">DA Moffat</name></author><author><name sortKey="Ramsden, Rt" uniqKey="Ramsden R">RT Ramsden</name></author><author><name sortKey="Shaw, Hj" uniqKey="Shaw H">HJ Shaw</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Langlais, Rp" uniqKey="Langlais R">RP Langlais</name></author><author><name sortKey="Miles, Da" uniqKey="Miles D">DA Miles</name></author><author><name sortKey="Van Dis, Ml" uniqKey="Van Dis M">ML Van Dis</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Monsour, Pa" uniqKey="Monsour P">PA Monsour</name></author><author><name sortKey="Young, Wg" uniqKey="Young W">WG Young</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Massey, Ew" uniqKey="Massey E">EW Massey</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Eagle, W" uniqKey="Eagle W">W Eagle</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Harma, R" uniqKey="Harma R">R Harma</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Eagle, W" uniqKey="Eagle W">W Eagle</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Murtagh, Rd" uniqKey="Murtagh R">RD Murtagh</name></author><author><name sortKey="Caracciolo, Jt" uniqKey="Caracciolo J">JT Caracciolo</name></author><author><name sortKey="Fernandez, G" uniqKey="Fernandez G">G Fernandez</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Lentini, A" uniqKey="Lentini A">A Lentini</name></author></analytic></biblStruct></listBibl></div1></back></TEI><pmc article-type="case-report"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Surg Case Rep</journal-id><journal-id journal-id-type="iso-abbrev">J Surg Case Rep</journal-id><journal-id journal-id-type="publisher-id">jscr</journal-id><journal-title-group><journal-title>Journal of Surgical Case Reports</journal-title></journal-title-group><issn pub-type="epub">2042-8812</issn><publisher><publisher-name>Oxford University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">28852461</article-id><article-id pub-id-type="pmc">5570094</article-id><article-id pub-id-type="doi">10.1093/jscr/rjx152</article-id><article-id pub-id-type="publisher-id">rjx152</article-id><article-categories><subj-group subj-group-type="heading"><subject>Case Report</subject></subj-group></article-categories><title-group><article-title>Case report: an atypical presentation of Eagle syndrome</article-title></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name><surname>Gallaway</surname><given-names>Edward</given-names></name><xref ref-type="aff" rid="rjx152af1">1</xref><xref ref-type="corresp" rid="rjx152cor1"></xref><pmc-comment>edward.gallaway@elht.nhs.uk </pmc-comment>
</contrib><contrib contrib-type="author"><name><surname>Bayoumi</surname><given-names>Sherif</given-names></name><xref ref-type="aff" rid="rjx152af2">2</xref></contrib><contrib contrib-type="author"><name><surname>Hammond</surname><given-names>Douglas</given-names></name><xref ref-type="aff" rid="rjx152af3">3</xref></contrib><contrib contrib-type="author"><name><surname>Halsnad</surname><given-names>Moorthy</given-names></name><xref ref-type="aff" rid="rjx152af4">4</xref></contrib></contrib-group><aff id="rjx152af1"><label>1</label><addr-line>Royal Blackburn Hospital, Blackburn, UK</addr-line></aff><aff id="rjx152af2"><label>2</label><addr-line>Pennine Acute Hospitals NHS Trust, Manchester, UK</addr-line></aff><aff id="rjx152af3"><label>3</label><institution>School of Dentistry, University of Central Lancashire</institution>,<addr-line>Preston, UK</addr-line></aff><aff id="rjx152af4"><label>4</label><addr-line>NHS Greater Glasgow and Clyde, Glasgow, UK</addr-line></aff><author-notes><corresp id="rjx152cor1"><label>*</label>Correspondence address. Royal Blackburn Teaching Hospital, Haslingden Rd, Blackburn BB2 3HH, UK. E-mail: <email>edward.gallaway@elht.nhs.uk</email></corresp></author-notes><pub-date pub-type="collection"><month>8</month><year>2017</year></pub-date><pub-date iso-8601-date="2017-08-01" pub-type="epub"><day>01</day><month>8</month><year>2017</year></pub-date><pub-date pub-type="pmc-release"><day>01</day><month>8</month><year>2017</year></pub-date><pmc-comment> PMC Release delay is 0 months and 0 days and was based on the
<volume>2017</volume><issue>8</issue><elocation-id>rjx152</elocation-id><history><date date-type="received"><day>04</day><month>5</month><year>2017</year></date><date date-type="accepted"><day>10</day><month>7</month><year>2017</year></date></history><permissions><copyright-statement>Published by Oxford University Press and JSCR Publishing Ltd. All rights reserved. © The Author 2017.</copyright-statement><copyright-year>2017</copyright-year><license license-type="cc-by-nc" xlink:href="http://creativecommons.org/licenses/by-nc/4.0/"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<uri xlink:href="http://creativecommons.org/licenses/by-nc/4.0/">http://creativecommons.org/licenses/by-nc/4.0/</uri>), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact <email>journals.permissions@oup.com</email></license-p></license></permissions><self-uri xlink:href="rjx152.pdf"></self-uri><abstract><title>Abstract</title><p>Elongation of the styloid process occurs in 4–7% of individuals. In the majority this elongation is asymptomatic. Presence of oropharyngeal pain and dysphagia with such elongation is known as Eagle syndrome. The aetiology of Eagle syndrome is believed to be a reactive osseus hyperplasia of the styloid process in response to pharyngeal trauma or surgical intervention, such as tonsillectomy. We present a case of a 72-year-old lady with a twelve month history of left sided oropharyngeal pain and worsening dysphagia, presenting with a long, slender, bony intraoral projection found to be an elongated styloid process. She previously underwent tonsillectomy and radiotherapy on the left side for a tonsillar carcinoma. Surgical reduction of the elongated styloid process via intraoral approach led to immediate post-operative pain relief and normal swallowing. We conclude that this atypical presentation of Eagle syndrome was caused by the patient's prior treatment for tonsillar carcinoma.</p></abstract><counts><page-count count="3"></page-count></counts></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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