Mehta J S, Sharr M M
Department of Neurosurgery, King's College Hospital, London, UK.
J Laryngol Otol. 1998 Feb;112(2):193-5. doi: 10.1017/s0022215100140290.
We report a case of a 40-year-old man presenting with acute vertigo and deafness. Computed tomography (CT) scanning at initial presentation was normal. However, one year later he developed numbness on the right side of his face and examination revealed fifth, seventh and eighth cranial nerve palsies as well as cerebellar dysfunction. Magnetic resonance imaging (MRI) demonstrated a cerebellopontine angle lesion. He underwent near total excision followed by neuro-axis irradiation. The main mass of the tumour projected into the cerebellopontine angle. Histology showed this to be a medulloblastoma. All features of this case are unusual; hence we discuss the pathogenesis and management of this very rare tumour.
我们报告一例40岁男性,表现为急性眩晕和耳聋。初诊时计算机断层扫描(CT)正常。然而,一年后他出现右侧面部麻木,检查发现有第五、第七和第八颅神经麻痹以及小脑功能障碍。磁共振成像(MRI)显示桥小脑角病变。他接受了次全切除,随后进行了神经轴照射。肿瘤的主要肿块突入桥小脑角。组织学检查显示为髓母细胞瘤。该病例的所有特征均不寻常;因此,我们讨论了这种非常罕见肿瘤的发病机制和治疗方法。