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使用三维计算机断层扫描技术对眼-耳-脊椎综合征进行临床胚胎学与放射学相关性研究

Clinical-embryological and radiological correlations of oculo-auriculo-vertebral spectrum using 3D-CT.

作者信息

Santos D T, Miyazaki O, Cavalcanti M G P

机构信息

Department of Radiology, College of Dentistry, University of São Paulo, São Paulo, SP, Brazil.

出版信息

Dentomaxillofac Radiol. 2003 Jan;32(1):8-14. doi: 10.1259/dmfr/36409607.

Abstract

OBJECTIVES

The purpose of this paper is to present a variety of imaging findings of oculo-auriculo-vertebral spectrum (Goldenhar syndrome) using three-dimensional reconstructed images from computed tomography (3D-CT), associating clinical and embryological patterns of the syndrome.

METHODS

The study population consisted of 10 patients with oculo-auriculo-vertebral spectrum with clinically identified hemifacial microsomia. The patients were examined using spiral CT, and abnormal imaging features were grouped under facial, ear and temporal bone, vertebral, and skull base anomalies. The original CT data were transferred to a networked computer workstation with a computer graphics system to generate 3D-CT volume rendered images of the skull and vertebra. Two observers analysed the bone and muscular setting protocols to assess the relationship between bone and muscular structures.

RESULTS

Asymmetric underdevelopment was a characteristic pattern of this syndrome resulting from hypoplasia of the mandibular ramus and condyle, the zygomatic, sphenoid and auricular conduct bones, and the temporal and masseter muscles. The syndrome was associated with local atrophy seen on 3D-CT images using specific bone and muscles protocols in all cases.

CONCLUSIONS

Understanding the aetiology, embryology and wide imaging spectrum of this syndrome is essential to make a correct diagnosis, for treatment planning, and for evaluation when associated with a 3D-CT computer graphics system.

摘要

目的

本文旨在通过计算机断层扫描三维重建图像(3D-CT)展示眼-耳-脊椎综合征(Goldenhar综合征)的多种影像学表现,并结合该综合征的临床和胚胎学模式。

方法

研究对象为10例经临床确诊为半侧颜面短小畸形的眼-耳-脊椎综合征患者。对患者进行螺旋CT检查,将异常影像学特征分为面部、耳及颞骨、脊椎和颅底异常。将原始CT数据传输至配备计算机图形系统的联网计算机工作站,以生成颅骨和脊椎的3D-CT容积再现图像。两名观察者分析骨骼和肌肉设置方案,以评估骨骼与肌肉结构之间的关系。

结果

不对称发育不全是该综合征的特征性模式,由下颌支和髁突、颧骨、蝶骨和耳传导骨以及颞肌和咬肌发育不全引起。在所有病例中,使用特定的骨骼和肌肉方案,该综合征与3D-CT图像上所见的局部萎缩相关。

结论

了解该综合征的病因、胚胎学和广泛的影像学表现对于正确诊断、治疗计划制定以及与3D-CT计算机图形系统相关联时的评估至关重要。

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