Gadiraju Sumana, Jacob Gregg A, Mazzola Catherine A
Norton College of Medicine, Upstate Medical University, Syracuse, NY, 13210, USA.
Northeast Facial and Oral Surgery Specialists, Florham Park, NJ, 07932, USA.
Childs Nerv Syst. 2024 Dec 23;41(1):65. doi: 10.1007/s00381-024-06727-8.
Goldenhar syndrome is a clinically heterogeneous disorder defined by a rare combination of congenital anomalies-an eye abnormality, in addition to two of the following three: ear anomalies, mandibular malformations, and vertebral defects. Notably, children with Goldenhar syndrome present with a high incidence of cervical spine malformations.
In this report, we present an unusual case of a 15-year-old child with Goldenhar syndrome, who additionally presents with some clinical features of VACTERL syndrome. The patient was scheduled for mandibular distraction surgery with oral maxillofacial surgery. It was noted on pre-operative three-dimensional computed tomography (3D CT) that there was mild basilar invagination and stenosis of the foramen magnum. A magnetic resonance imaging (MRI) study was recommended and showed cervicomedullary compression, for which a suboccipital craniectomy and C1 laminectomy were performed.
Considering the cervical spine anomalies in Goldenhar syndrome, we describe precautions to manage the risk of cervical spinal cord injury during general anesthesia, including pre-operative evaluation for cervical spine compression and/or instability and minimizing neck movement during intubation. For the latter, we recommend a controlled, neutral neck position during intubation, operation, and recovery.
Goldenhar综合征是一种临床异质性疾病,由先天性异常的罕见组合所定义——一种眼部异常,此外还伴有以下三项中的两项:耳部异常、下颌骨畸形和脊柱缺损。值得注意的是,Goldenhar综合征患儿颈椎畸形的发生率很高。
在本报告中,我们介绍了一例不同寻常的病例,一名15岁患有Goldenhar综合征的儿童,还表现出一些VACTERL综合征的临床特征。该患者计划接受口腔颌面外科的下颌骨牵张手术。术前三维计算机断层扫描(3D CT)显示存在轻度基底凹陷和枕骨大孔狭窄。建议进行磁共振成像(MRI)检查,结果显示颈髓受压,为此实施了枕下颅骨切除术和C1椎板切除术。
考虑到Goldenhar综合征中的颈椎异常,我们描述了在全身麻醉期间管理颈脊髓损伤风险的注意事项,包括对颈椎压迫和/或不稳定进行术前评估,以及在插管期间尽量减少颈部活动。对于后者,我们建议在插管、手术和恢复期间保持颈部处于可控的中立位置。