Hanabusa K, Morikawa A, Murata T, Taki W
Department of Neurosurgery and Pathology, Suzuka General Hospital, Tsu, Mie, Japan.
J Neurosurg. 2001 Sep;95(3):518-21. doi: 10.3171/jns.2001.95.3.0518.
The authors describe the case of a 57-year-old woman who had a right-sided hearing disturbance that had remained untreated for 1 year. The diagnosis was of a right cerebellopontine angle tumor, and the patient underwent its removal via retrosigmoid approach. Pathologically, the tumor was a typical benign neuroma. Growth of residual tumor was detected 4 years after the initial operation, and it was treated with gamma knife surgery (GKS). Six months later, the tumor had grown, and the patient underwent surgery via a combined retrosigmoid-translabyrinthine approach. Abnormal mitotic figures were observed on histological studies, indicating that the tumor had become malignant. Thereafter, the tumor grew rapidly, and the patient died 6.5 years after the initial treatment. It cannot be ruled out that GKS affected the outcome, but the causal sequence was unclear. Because such a patient is rare, documentation of the case was considered clinically important.
作者描述了一名57岁女性的病例,该患者右侧听力障碍,未经治疗长达1年。诊断为右侧桥小脑角肿瘤,患者通过乙状窦后入路进行了肿瘤切除。病理检查显示,肿瘤为典型的良性神经瘤。初次手术后4年检测到残留肿瘤生长,遂采用伽玛刀手术(GKS)进行治疗。6个月后,肿瘤继续生长,患者通过乙状窦后-迷路联合入路接受了手术。组织学研究观察到异常有丝分裂象,表明肿瘤已恶变。此后,肿瘤迅速生长,患者在初次治疗后6.5年死亡。不能排除GKS对结果产生了影响,但因果关系尚不清楚。由于此类患者罕见,该病例记录被认为具有临床重要性。