Abstract

Purpose: Eagle syndrome is a rare symptomatic clinical and radiological entity. It is characterized by an elongation of the styloid process or calcification of the stylohyoid ligament, and it typically causes head and neck pain, odynophagia, otalgia, or headache. Observation: The first case dealt with an elongation of the left styloid by 46 mm, and the second case dealt with a calcification of the right stylohyoid ligament at the lesser horn of the hyoid bone. In both cases, cervical rotation caused a vagal episode by the compression of the carotid arteries. Both cases were treated surgically, the first with an intrabuccal procedure and the second by cervicotomy. Both patients have shown no postoperative recurrence of their symptoms. Conclusion: Eagle syndrome, although rare, should be considered when patients describe pain symptoms with no identified etiology in the head and neck area. A simple additional diagnostic procedure such as a computed tomography (CT) scan or an orthopantomogram can easily show a long styloid process or calcified stylohyoid ligament and their anatomical relations, in particular, any vascular relations. The use of piezosurgery decreases intraoperative risks in the mastoid cut of styloid process.

Highlights

  • Described for the first time by Eagle in 1937 [1], Eagle syndrome consists of a set of symptoms of the head and neck region

  • Its etiology is the calcification of the stylohyoid ligament or elongation of the styloid process over the average length of 25 mm, and it affects approximately 5% of the population [2]

  • We present two clinical cases: the first is a typical elongation of the styloid process and the second is an ossification of the lower segment of the stylohyoid ligament, in level with the lesser horn of the hyoid bone

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Summary

Introduction

Described for the first time by Eagle in 1937 [1], Eagle syndrome consists of a set of symptoms of the head and neck region. Its etiology is the calcification of the stylohyoid ligament or elongation of the styloid process over the average length of 25 mm, and it affects approximately 5% of the population [2]. The classical clinical presentation is a unilateral oropharyngeal pain, exacerbated by swallowing, tonsillar fossa palpation, or cephalic torsion [2]. We present two clinical cases: the first is a typical elongation of the styloid process and the second is an ossification of the lower segment of the stylohyoid ligament, in level with the lesser horn of the hyoid bone.

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