Revista de Gastroenterología de México Revista de Gastroenterología de México
Rev Gastroenterol Mex 2017;82:257-8 - Vol. 82 Num.3 DOI: 10.1016/j.rgmxen.2017.05.005
Clinical image in Gastroenterology
Eagle syndrome as an uncommon cause of dysphagia
Síndrome de Eagle como causa infrecuente de disfagia
S. Benet-Muñoz, , L. Tacoronte-Pérez, R. Fernández-Belda, J.J. Artazkoz-del Toro
Otorhinolaryngology Service, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain

A 57-year-old man with an unremarkable past history sought an otorhinolaryngology consultation for symptoms of oropharyngeal dysphagia and an ever-increasing sensation of a foreign body. Physical examination and fiberoptic nasopharyngoscopy were normal, and so an extension study was carried out. The computerized tomography scan of the neck showed a lengthening of both styloid apophyses, 5cm on the left side and 7cm on the right (Fig. 1). The patient was diagnosed with Eagle syndrome. Given the disease progression and the patient's clinical progression, we decided to resect both styloid apophyses and posterior hyoid horns (Figs. 2 and 3). The patient had satisfactory postoperative progression.

Figure 1.

CT image of elongation of both styloid apophyses.

Figure 2.

Endoscopic image during the surgery.

Figure 3.

Resection of both styloid apophyses (upper part of the image) and both horns of the hyoid bone (lower part of the image).

Eagle syndrome, first described in 1937, is an entity with characteristic symptomatology caused by the elongation of the styloid apophyses. There is a 3.3% prevalence of elongations of the styloid apophyses, and 4% of those cases may present with symptoms.1,2 In Eagle syndrome, said elongations can be accompanied with pharyngeal pain, oropharyngeal dysphagia, the sensation of a foreign body, orofacial pain, and ATM dysfunction and/or carotidynia.1,2 Conventional radiologic studies can reveal the elongation of the styloid apophyses, but computed tomography provides a better description of the anatomic structures and improved preoperative planning.1,3 Treatment of this entity depends on the patient's symptoms, and the treatment of choice is resection of the styloid apophyses.1

Ethical disclosuresProtection of human and animal subjects

The authors declare that the procedures followed were in accordance with the regulations of the relevant clinical research ethics committee and with those of the Code of Ethics of the World Medical Association (Declaration of Helsinki).

Confidentiality of data

The authors declare that they have followed the protocols of their work center on the publication of patient data.

Right to privacy and informed consent

The authors declare that no patient data appear in this article.

Conflict of interest

The authors declare that there is no conflict of interest.

J. Mareque-Bueno,F. Hernández-Alfaro,M.J. Biosca-de Tejada
Abordaje Intraoral en el síndrome de Eagle. Presentación de un caso clínico
Rev Esp Cir Oral Maxilofac., 33 (2011), pp. 157-161
S.R. Nazar,G.A. Naser,O.J. Fullá
Si??ndrome de Eagle en Otorrinolaringologi??a
Rev Hosp Cli??n Univ Chile, 19 (2008), pp. 156-161
J.L. Hernández,R. Rodríguez-Sánchez,J.L. de Serdio-Arias
Autoarrancamiento de apófisis estiloides en síndrome de Eagle
Acta Otorrinolaringol Esp., 65 (2014), pp. 322-323

Please cite this article as: Benet-Muñoz S, Tacoronte-Pérez L, Fernández-Belda R, Artazkoz-del Toro JJ. Síndrome de Eagle como causa infrecuente de disfagia. Revista de Gastroenterología de México. 2017;82:257–258.

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Copyright © 2017. Asociación Mexicana de Gastroenterología
Rev Gastroenterol Mex 2017;82:257-8 - Vol. 82 Num.3 DOI: 10.1016/j.rgmxen.2017.05.005