Finneran Megan, Marotta Dario A, Altenburger Dana, Nardone Emilio
Neurosurgery, Advocate BroMenn Medical Center, Normal, USA.
Department of Research, Alabama College of Osteopathic Medicine, Dothan, USA.
Cureus. 2020 Feb 7;12(2):e6914. doi: 10.7759/cureus.6914.
Butterfly glioblastoma (bGBM) is a malignant glioma that crosses the corpus callous with bilateral cerebral hemisphere involvement. Literature reports are scarce and highlight a dismal prognosis with limited successful treatment options. We describe a patient who survived more than five years from the initial diagnosis. A 44-year-old woman presented to the emergency room for evaluation one day after a motor vehicle collision at the insistence of her husband, with four weeks of confusion, behavioral changes, and increased fatigue. Magnetic resonance imaging (MRI) of the brain revealed an enhancing, heterogeneous mass with significant necrosis, centered in the septum pellucidum and corpus callosum with intraventricular extension. She underwent a stereotactic biopsy of the lesion. Pathology was consistent with glioblastoma, WHO grade IV. She underwent standard radiation treatment and adjuvant temozolomide, demonstrating a near-complete disappearance of the tumor on imaging for the subsequent two years. Upon recurrence, she underwent additional chemotherapy with limited response. A repeat biopsy was positive for a mutation and she was treated with lomustine. After two cycles, she developed thrombocytopenia and shortly after elected to discontinue treatment. She succumbed to the progression of disease five years and two months after the initial presentation. bGBMs are uncommon and highly aggressive brain tumors. A tailored treatment protocol may improve survival. This case marks an unusually long survival of a patient with bGBM and may prompt further research to better understand the behavior of these tumors and how to improve treatment response and survival.
蝶形胶质母细胞瘤(bGBM)是一种恶性胶质瘤,可穿过胼胝体,累及双侧大脑半球。文献报道稀少,且突出显示其预后不佳,成功的治疗选择有限。我们描述了一名从初始诊断起存活超过五年的患者。一名44岁女性在其丈夫的坚持下,于机动车碰撞一天后到急诊室进行评估,她已经困惑、行为改变并疲劳加重四周。脑部磁共振成像(MRI)显示一个强化的、不均匀的肿块,伴有明显坏死,以透明隔和胼胝体为中心,并向脑室内延伸。她接受了病变的立体定向活检。病理结果符合WHO四级胶质母细胞瘤。她接受了标准放疗和辅助替莫唑胺治疗,在随后两年的影像学检查中显示肿瘤几乎完全消失。复发后,她接受了额外化疗,但反应有限。重复活检显示一种突变呈阳性,她接受了洛莫司汀治疗。两个周期后,她出现血小板减少症,不久后选择停止治疗。她在首次就诊五年零两个月后因疾病进展而死亡。bGBM是罕见且高度侵袭性的脑肿瘤。量身定制的治疗方案可能会提高生存率。该病例标志着一名bGBM患者异常长的生存期,可能会促使进一步研究,以更好地了解这些肿瘤的行为以及如何改善治疗反应和生存率。