Shibahara Ichiyo, Kawaguchi Tomohiro, Kanamori Masayuki, Yonezawa Shingo, Takazawa Hiroki, Asano Kenichiro, Ohkuma Hiroki, Kaimori Mitsuomi, Sasaki Tatsuya, Nishijima Michiharu
Department of Neurosurgery, Aomori Prefectural Central Hospital, Aomori, Japan.
Neurol Med Chir (Tokyo). 2011;51(2):144-7. doi: 10.2176/nmc.51.144.
Pilocytic astrocytoma sometimes transforms to a malignant type, and previous radiation therapy is considered to be a key factor. We report a case of pilocytic astrocytoma with histological malignant features without previous radiation therapy. A 21-year-old man presented a sudden onset of severe headache. Neuroimaging had detected a cystic mass in the posterior fossa at the age of one year without therapeutic intervention. On admission, computed tomography depicted a brain tumor in the posterior fossa with cystic components, intratumoral hemorrhage, and upward herniation. Urgent surgery was performed, and histological examination revealed some features of pilocytic astrocytoma but also broad necrosis, high cellularity, and MIB-1 labeling index of more than 20%. The histological diagnosis was pilocytic astrocytoma with malignant features. This tumor had continued a benign clinical course for 20 years, but had eventually transformed to a malignant type. Therefore, pilocytic astrocytoma may undergo spontaneous malignant transformation during its natural clinical course.
毛细胞型星形细胞瘤有时会转变为恶性类型,既往放疗被认为是一个关键因素。我们报告一例具有组织学恶性特征但既往未接受过放疗的毛细胞型星形细胞瘤病例。一名21岁男性突发剧烈头痛。神经影像学检查在其1岁时发现后颅窝有一个囊性肿块,未进行治疗干预。入院时,计算机断层扫描显示后颅窝有一个脑肿瘤,伴有囊性成分、瘤内出血和向上疝出。紧急进行了手术,组织学检查显示有一些毛细胞型星形细胞瘤的特征,但也有广泛坏死、高细胞密度以及MIB-1标记指数超过20% 的情况。组织学诊断为具有恶性特征的毛细胞型星形细胞瘤。该肿瘤在20年的时间里一直保持良性临床病程,但最终转变为恶性类型。因此,毛细胞型星形细胞瘤在其自然临床病程中可能会发生自发恶性转化。