Hossein Rekabi, Kambiz Mohammadi, Mohammad Davoody, Mina Najarzade
Department of Otolaryngology, Head and Neck Surgery, Ahwaz University of Medical Sciences, Ahwaz, Iran.
J Craniofac Surg. 2010 Jan;21(1):275-6. doi: 10.1097/SCS.0b013e3181c5a444.
Eagle syndrome is considered a rare disease. It is an aggregation of symptoms that includes neck, throat, and hemifacial pain; sensation of foreign body in the throat; dysphagia; otalgia; and change in voice as a direct result of an elongated styloid process or calcified stylohyoid ligament.The clinical diagnosis is generally difficult and must be confirmed by radiologic imaging. Our patient was a 37-year-old woman who had a 3 years' history of dysphagia and foreign body sensation. Computed tomographic scan showed a long left styloid process and calcification in the upper part of the stylohyoid ligament suggestive of Eagle syndrome. The patient underwent surgical removal of the elongated styloid process through an intraoral approach. The patient became symptom-free at 9 months after the surgery.
鹰嘴综合征被认为是一种罕见疾病。它是一组症状的集合,包括颈部、咽喉和半侧面部疼痛;咽喉部异物感;吞咽困难;耳痛;以及由于茎突过长或茎突舌骨韧带钙化直接导致的声音改变。临床诊断通常较为困难,必须通过影像学检查来确诊。我们的患者是一名37岁女性,有3年吞咽困难和异物感病史。计算机断层扫描显示左侧茎突过长,茎突舌骨韧带上部钙化,提示鹰嘴综合征。患者通过口内入路接受了手术切除过长的茎突。术后9个月患者症状消失。