Otero-Rodríguez A, Sarabia-Herrero R, García-Tejeiro M, Zamora-Martínez T
Servicios de Neurocirugía, Hospital Clínico Universitario, Valladolid, España.
Neurocirugia (Astur). 2010 Jun;21(3):245-52. doi: 10.1016/s1130-1473(10)70084-1.
Pilocytic astrocytoma (PA) is a circumscribed neoplasia considered as a grade I astrocytoma by the World Health Organization. Its most common location is the cerebellum and it develops during the first two decades of the life. Prognosis is mostly excellent if gross-total resection can be achieved, with 10-year survival rates of up to 80%. Anaplastic or malignant transformation (MT) can rarely occur and is usually related to previous radiation. Spontaneous MT has exceptionally been reported. Histological criteria for diagnosis of MT are unclear, so no consensus exists. We present an atypical case of MT of a frontal PA without previous radiotherapy in a 28 years old patient. Also, we review the literature about prognostic factors of PA and discuss histological features that are considered as anaplastic or malignant in the PA.
毛细胞型星形细胞瘤(PA)是一种边界清楚的肿瘤,被世界卫生组织视为I级星形细胞瘤。其最常见的部位是小脑,多在生命的前二十年发生。如果能实现全切,预后大多良好,10年生存率高达80%。间变或恶性转化(MT)很少发生,通常与既往放疗有关。曾有过自发性MT的罕见报道。MT的组织学诊断标准尚不明确,因此尚未达成共识。我们报告了一例28岁未曾接受过放疗的额叶PA发生MT的非典型病例。此外,我们回顾了有关PA预后因素的文献,并讨论了PA中被视为间变或恶性的组织学特征。