Akay Kamil Melih, Erdogan Ersin, Izci Yusuf, Kaya Ayper, Timurkaynak Erdener
Department of Neurosurgery, Gulhane Military Medical Academy, Ankara, Turkey.
Neurol Med Chir (Tokyo). 2003 Nov;43(11):555-8. doi: 10.2176/nmc.43.555.
A 21-year-old male patient presented with a rare cerebellopontine angle medulloblastoma manifesting as cerebellar and long tract involvement signs and symptoms. The clinical and radiological characteristics of the lesion were similar to extraaxial lesions of cerebellopontine angle. The histological diagnosis of the lesion was medulloblastoma. Surgery achieved partial removal and was followed by radiotherapy and chemotherapy. The patient remained well after 18 months. Medulloblastoma of the cerebellopontine angle is a relatively rare clinical entity and may occur as a dural-based extraaxial mass.
一名21岁男性患者出现罕见的小脑桥脑角髓母细胞瘤,表现为小脑及长束受累的体征和症状。该病变的临床和影像学特征与小脑桥脑角的轴外病变相似。病变的组织学诊断为髓母细胞瘤。手术实现了部分切除,随后进行了放疗和化疗。18个月后患者情况良好。小脑桥脑角髓母细胞瘤是一种相对罕见的临床实体,可能以硬脑膜为基底的轴外肿块形式出现。