Vollmer Kathrin, Pantazis Georgios, Añon Javier, Roelcke Ulrich, Schwyzer Lucia
Department of Oncology, Kantonsspital Aarau, Aarau, Switzerland.
Department of Pathology, Kantonsspital Aarau, Aarau, Switzerland.
World Neurosurg X. 2019 Feb 12;2:100019. doi: 10.1016/j.wnsx.2019.100019. eCollection 2019 Apr.
Glioblastoma multiforme with a primitive neuronal component is a rare entity, with few cases reported in the literature.
A patient who had a supratentorial glioblastoma multiforme with a primitive neuronal component developed spinal metastasis during the disease course. With his history of leukemia during childhood, he was likely exposed to therapeutic ionizing brain radiation, which could have increased the risk of developing brain cancer in adulthood.
The range of incidence rates of dissemination in the literature is 2%-4%, typically in cases of cerebellar glioblastoma multiforme, but as high as 25% in autopsy series. Our case highlights several other topics in the literature, such as immunohistochemical patterns that differ between the primary tumor and spinal metastases and dissemination locations, typically leptomeningeal or ventricular invasion.
伴有原始神经成分的多形性胶质母细胞瘤是一种罕见的实体瘤,文献报道的病例较少。
一名患有伴有原始神经成分的幕上多形性胶质母细胞瘤的患者在病程中发生了脊髓转移。由于他童年时有白血病病史,他可能接受过脑部治疗性电离辐射,这可能增加了成年后患脑癌的风险。
文献中报道的播散发生率范围为2%-4%,通常见于小脑多形性胶质母细胞瘤病例,但在尸检系列中高达25%。我们的病例突出了文献中的其他几个主题,例如原发性肿瘤与脊髓转移瘤之间不同的免疫组化模式以及播散部位,通常为软脑膜或脑室侵犯。