Kang Ho, Kim Jin Wook, Se Young-Bem, Park Sung-Hye
Department of Neurosurgery, Seoul National University Hospital, Seoul, Korea.
Department of Pathology, Seoul National University Hospital, Seoul, Korea.
J Korean Neurosurg Soc. 2016 May;59(3):302-5. doi: 10.3340/jkns.2016.59.3.302. Epub 2016 May 10.
Gliofibroma is an extremely rare biphasic tumor with an astrocytic and benign mesenchymal component, which commonly occurs within the first two decades of life. The exact biological behavior of the tumor is not fully understood. Therefore, it is not listed as a distinct entity in the current World Health Organization classification of central nervous system tumors. Here, we describe a rare case of gliofibroma, which was located on the medial temporal lobe in a 61-year-old woman. Preoperatively, we misdiagnosed it as a meningioma because it was a well-demarcated and well-enhanced extra-axial mass with calcification and bony destruction. On the histopathological and immunohistochemical examination, the tumor consisted of a mixture of glial tissue and mesenchymal tissue and it was finally diagnosed as a gliofibroma. To our knowledge, this case of intracranial gliofibroma is in the oldest patient ever reported.
胶质纤维瘤是一种极其罕见的双相肿瘤,具有星形细胞和良性间充质成分,通常发生在生命的前二十年。肿瘤的确切生物学行为尚未完全了解。因此,在世界卫生组织目前的中枢神经系统肿瘤分类中,它未被列为一个独立的实体。在此,我们描述一例罕见的胶质纤维瘤病例,该病例位于一名61岁女性的颞叶内侧。术前,我们将其误诊为脑膜瘤,因为它是一个边界清晰、强化良好的轴外肿块,伴有钙化和骨质破坏。经组织病理学和免疫组织化学检查,肿瘤由神经胶质组织和间充质组织混合组成,最终被诊断为胶质纤维瘤。据我们所知,该例颅内胶质纤维瘤患者是有报道以来年龄最大的。