*Department of Diagnostic and Interventional Neuroradiology, Hoppe-Seyler-Straße 3; and †Department of Otorhinolaryngology, Elfriede-Aulhorn-Straße 5, Tübingen, Germany.
Otol Neurotol. 2014 Jun;35(5):826-30. doi: 10.1097/MAO.0000000000000278.
Goldenhar syndrome is a developmental disorder presenting with orofacial and vertebral anomalies, which are also accompanied by abnormalities in other organs. We examined temporal bone changes with special emphasis on inner ear abnormalities in these patients.
A retrospective review of 7 new cases in addition to a previously published series of 14 cases with clinically diagnosed Goldenhar syndrome was carried out to search for inner ear anomalies. In addition, temporal bone imaging studies from the literature were summarized and compared with our results.
Departments of Neuroradiology and Otorhinolaryngology at a university hospital.
In addition to the previous series of 14 patients, 7 new patients with Goldenhar syndrome were identified.
Patients underwent otologic examination, audiometric studies, and high-resolution computed tomography (CT) or magnetic resonance imaging (MRI) of the temporal bone.
Temporal bone changes and specifically inner ear malformations.
Nineteen of 21 patients showed changes of the external and middle ear correlating with the literature. Seven of 21 patients showed inner ear abnormalities constituting one-third of all patients. These ranged from mild such as vestibular enlargement to severe defects such as cochlear hypoplasia and common cavity.
Inner ear abnormalities were present in one-third of patients. Although in some cases, these might not be of clinical significance, some patients show severe defects of the inner ear requiring more complex hearing loss therapy. Therefore, imaging of the temporal bone structures is important in the care of these patients.
Goldenhar 综合征是一种发育障碍性疾病,表现为颌面和脊柱异常,同时还伴有其他器官的异常。我们检查了这些患者的颞骨变化,特别强调了内耳异常。
对新诊断的 7 例 Goldenhar 综合征患者(此外,还对之前发表的 14 例临床诊断为 Goldenhar 综合征患者的系列病例进行了回顾性分析)进行回顾性研究,以寻找内耳异常。此外,我们还对文献中的颞骨影像学研究进行了总结,并与我们的结果进行了比较。
一所大学医院的神经放射科和耳鼻喉科。
除了之前的 14 例患者系列外,还发现了 7 例新的 Goldenhar 综合征患者。
患者接受了耳科学检查、听力研究以及颞骨高分辨率计算机断层扫描(CT)或磁共振成像(MRI)检查。
颞骨变化,特别是内耳畸形。
21 例患者中有 19 例出现了与文献相符的外耳和中耳变化。21 例患者中有 7 例出现内耳异常,占所有患者的三分之一。这些异常范围从单纯的前庭扩大到严重的耳蜗发育不全和共同腔等缺陷。
内耳异常在三分之一的患者中存在。尽管在某些情况下,这些异常可能没有临床意义,但有些患者表现出严重的内耳缺陷,需要更复杂的听力损失治疗。因此,颞骨结构的影像学检查对这些患者的治疗非常重要。