


Often patients who are distressed after suffering from diagnostic failures, and after having completed courses of medication to no avail, will turn to an ENT specialist to find a remedy for the numerous pains they are experiencing.
There are symptoms that, due to their low frequency of occurrence, may be unknown even to the doctor. A doctor may dismiss them, or not be able to make a connection between the symptoms. Without previous experience, Eagle Syndrome is difficult to recognise.
Everyone has a tusk-shaped bone of 4-5cm in length on each side of the base of the skull. . They are called styloid processes and, with the stylo-hyoid ligament, attach the skull to the hyoid bone in the neck. When one or both ligaments ossify or calcify, they give rise to Eagle Syndrome. It is a very rare disorder.
The diagnosis of a patient with Eagle Syndrome is based on the presence of a series of symptoms to which it’s difficult to find an explanation.
Common symptoms include:
The only treatment for Eagle Syndrome is surgery. It consists of the removal of the ligament that is ossified, and can be done in two ways:
Anna, a patient, explains it this way: "I had just had a son. For more than three years I had been to see countless specialists who gave me lots of medication. I was very nervous and stressed with having a new baby. Many visits were depressing and I learned that you should be careful telling the doctor about your state of mind, as it was leading them to a diagnosis of depression or anxiety."
"It is very frustrating to see that nobody understands you and think that you may have to spend the rest of your life with that unbearable pain. I ended up thinking I had lymphoma. It was not until I was diagnosed and operated on that I was able to go back to being the person I had been before: a healthy and happy person."