Cai Ning, Kahn Leonard B
Department of Pathology, Long Island Jewish Medical Center, Long Island Campus for the Albert Einstein College of Medicine, New Hyde Park, NY 11040, USA.
J Neurooncol. 2004 Jun;68(2):161-7. doi: 10.1023/b:neon.0000027740.70380.5c.
Primary fibrosarcoma of the central nervous system (CNS) is an extremely rare tumor. To the best of our knowledge, only 40 cases have been reported in the literature. We document such a case in a 9-year-old child who presented with a short history of headache and vomiting. A mass was completely removed and histologic examination revealed a primary fibrosarcoma with features resembling solitary fibrous tumor, meningioma, and malignant fibrous histiocytoma. In addition, the tumor was associated with meningioangiomatosis. A primary CNS fibrosarcoma with these features is most unusual and rendered a precise diagnosis difficult.
中枢神经系统原发性纤维肉瘤是一种极为罕见的肿瘤。据我们所知,文献中仅报道过40例。我们记录了这样一例发生在一名9岁儿童身上的病例,该患儿有短暂的头痛和呕吐病史。肿瘤被完整切除,组织学检查显示为原发性纤维肉瘤,其特征类似于孤立性纤维瘤、脑膜瘤和恶性纤维组织细胞瘤。此外,该肿瘤与脑膜血管外皮细胞瘤相关。具有这些特征的原发性中枢神经系统纤维肉瘤非常罕见,难以做出准确诊断。