Spurgeon Angela, Le Viet, Konakondla Sanjay, Miller Douglas C, Hopkins Tamera, Litofsky N Scott
Division of Neurosurgery, University of Missouri School of Medicine, Columbia, MO 65212, USA.
University of Missouri School of Medicine, Columbia, MO 65212, USA.
Case Rep Neurol Med. 2016;2016:6813089. doi: 10.1155/2016/6813089. Epub 2016 May 8.
Background. High-grade gliomas of the brainstem are rare in adults and are particularly rare in the anterolateral medulla. We describe an illustrative case and discuss the diagnostic and treatment issues associated with a tumor in this location, including differential diagnosis, anatomical considerations for options for surgical management, multimodality treatment, and prognosis. Case Description. A 69-year-old woman presented with a 3-week history of progressive right lower extremity weakness. She underwent an open biopsy via a far lateral approach with partial condylectomy, which revealed a glioblastoma. Concurrent temozolomide and radiation were completed; however, she elected to stop her chemotherapy after 5.5 weeks of treatment. She succumbed to her disease 11 months after diagnosis. Conclusions. Biopsy can be performed relatively safely to provide definitive diagnosis to guide treatment, but long-term prognosis is poor.
背景。脑干高级别胶质瘤在成人中罕见,在前外侧延髓尤为罕见。我们描述一例典型病例,并讨论与该部位肿瘤相关的诊断和治疗问题,包括鉴别诊断、手术治疗选择的解剖学考量、多模态治疗及预后。病例描述。一名69岁女性,有3周进行性右下肢无力病史。她通过远外侧入路行开放性活检并部分髁突切除术,结果显示为胶质母细胞瘤。同步进行了替莫唑胺化疗和放疗;然而,治疗5.5周后她选择停止化疗。诊断11个月后,她死于该疾病。结论。活检可相对安全地进行以提供明确诊断来指导治疗,但长期预后较差。