Fagan P A, Misra S N, Doust B
St. Vincent's Hospital, Sydney, Australia.
Laryngoscope. 1993 Apr;103(4 Pt 1):442-6. doi: 10.1002/lary.5541030414.
Four cases of facial neuroma confined to the cerebellopontine angle and internal auditory canal are presented. Prior to surgery, three of these were diagnosed as an acoustic tumor. At operation the true diagnosis of facial neuroma was made. The operative procedure was recorded on film and videotape. The magnetic resonance imaging (MRI) and computed tomography (CT) scans were reviewed retrospectively. In the first three cases the tumor was not centered on the axis of the internal auditory canal (IAC), as would be typical of an acoustic neuroma, but instead occupied a position eccentric to this axis. In one case, this eccentricity was marked. A similar appearance in the fourth case enabled the true diagnosis of facial neuroma to be made before surgery. The postoperative behavior of the tumors was unpredictable. The patient with the largest tumor, which was debulked at operation, did not develop a facial palsy. However, a patient with a small tumor which was not biopsied, developed a delayed but complete paralysis from which she subsequently recovered. This small series suggests that it may be possible, by use of the appropriate imaging technique, to diagnose, preoperatively, a cerebellopontine angle facial neuroma which is otherwise indistinguishable from an acoustic neuroma.
本文报告了4例局限于桥小脑角和内耳道的面神经瘤。术前,其中3例被诊断为听神经瘤。手术时确诊为面神经瘤。手术过程进行了电影和录像记录。对磁共振成像(MRI)和计算机断层扫描(CT)进行了回顾性分析。在前3例中,肿瘤并非像听神经瘤那样以内耳道(IAC)轴为中心,而是位于该轴的偏心位置。在1例中,这种偏心很明显。第4例的类似表现使得在手术前就能确诊为面神经瘤。肿瘤的术后表现不可预测。术中肿瘤大部分被切除的最大肿瘤患者未出现面瘫。然而,1例未进行活检的小肿瘤患者出现了延迟性但完全性的面瘫,随后恢复。这一小组病例表明,通过使用适当的成像技术,术前有可能诊断出与听神经瘤难以区分的桥小脑角面神经瘤。