Department of Neuroradiology, Cavale Blanche Brest University Hospital, boulevard Tanguy-Prigent, 29200 Brest, France.
J Neuroradiol. 2012 Mar;39(1):57-63. doi: 10.1016/j.neurad.2011.10.002. Epub 2011 Dec 15.
Isolated congenital anomalies of the stapes are infrequent but highly variable. The goal of this study is to present the numerous observed anomalies based on a large number of cases, and to describe anatomical variations and malformations of the stapes using high-resolution computed tomography (CT), after proper reorientation in the "axial stapes" plane.
The 1805 CT of temporal bones performed during the past 5 years have been retrospectively studied. After reconstructing the images in the stapes axial plane, the ears presenting a congenital anomaly of the stapes were included in this study. All the ears with acquired lesions were excluded. The anomalies have been sorted according to the affected part of the stapes: the superstructure, the footplate or the obturator foramen. Two neuroradiologists classified the anomalies as either anatomical variation, malformation, or undetermined.
Sixty-one stapes in 47 patients were found to have one or more congenitally abnormal shapes (bilateral anomalies were found in 14 of these patients). The abnormal part of the stapes was the superstructure in 17 cases, the footplate in 13 cases, the obturator foramen in 19 cases (with a high frequency of "double stapes" shape) while in 12 cases multiple parts were affected.
The use of ossicle reconstructions in the "axial stapes" plane with current multislice CT allows analyzing even minor congenital anomalies of the stapes. The boundaries between normal variations and malformations are sometimes difficult to set, especially when anomalies are minor. Malformations are more easily diagnosed when multiple parts of the stapes are affected.
孤立性镫骨先天性畸形较为罕见,但表现形式多样。本研究旨在通过大量病例展示所观察到的多种畸形,并在“镫骨轴位”适当重定向后,使用高分辨率计算机断层扫描(CT)描述镫骨的解剖变异和畸形。
回顾性研究过去 5 年期间进行的 1805 例颞骨 CT。在重建镫骨轴位图像后,将存在镫骨先天性畸形的耳朵纳入本研究。所有存在获得性病变的耳朵均被排除。根据病变累及的镫骨部位对畸形进行分类:镫骨上部、镫骨底板或镫骨导孔。两名神经放射科医生将畸形分为解剖变异、畸形或不确定。
在 47 名患者的 61 只耳朵中发现存在一个或多个先天性异常形态(这些患者中有 14 例存在双侧异常)。异常的镫骨部位为:17 例为镫骨上部,13 例为镫骨底板,19 例为镫骨导孔(“双镫骨”形态高发),12 例为多个部位受累。
目前多层螺旋 CT 可在“镫骨轴位”重建图像,有助于分析即使是较小的镫骨先天性畸形。正常变异和畸形之间的界限有时难以划定,尤其是当畸形较小时。当多个镫骨部位受累时,畸形更容易诊断。