Alexiou G A, Moschovi M, Stefanaki K, Prodromou C, Sfakianos G, Prodromou N
Department of Neurosurgery, Children's Hospital "Agia Sofia", Athens, Greece.
Neuropediatrics. 2010 Aug;41(2):69-71. doi: 10.1055/s-0030-1255094. Epub 2010 Aug 26.
Pleomorphic xanthoastrocytoma (PXA) is a recently recognized rare cerebral neoplasm that predominantly affects young patients. We report on the case of a 3-year-old boy who presented with a 2-week history of headaches and seizures. Radiological investigation revealed a lesion in the right parietal-occipital lobe. The lesion was excised and histology disclosed the presence of a PXA with anaplastic features. 1 year later follow-up magnetic resonance imaging (MRI) revealed tumor relapse. An MRI of the spine was also performed and demonstrated leptomeningeal dissemination. The patient underwent a second operation. Histology revealed that the presence of a malignant PXA with anaplastic features. The patient received radiotherapy and 9 months later on follow-up MRI a new tumor recurrence was noted. A third craniotomy was performed and the tumor removed. Histological examination revealed dedifferentiation to glioblastoma multiforme. The patient was referred to the oncology department and received chemotherapy with temozolamide. 8 months later the patient was stable without tumor recurrence. PXAs require close follow-up because of their unpredictable biological behaviour.
多形性黄色星形细胞瘤(PXA)是一种最近才被认识的罕见脑肿瘤,主要影响年轻患者。我们报告了一名3岁男孩的病例,他有2周的头痛和癫痫病史。影像学检查发现右侧顶枕叶有一个病变。该病变被切除,组织学检查显示存在具有间变特征的PXA。1年后的随访磁共振成像(MRI)显示肿瘤复发。还进行了脊柱MRI检查,显示有软脑膜播散。患者接受了第二次手术。组织学检查显示存在具有间变特征的恶性PXA。患者接受了放疗,9个月后的随访MRI发现有新的肿瘤复发。进行了第三次开颅手术并切除了肿瘤。组织学检查显示已分化为多形性胶质母细胞瘤。患者被转诊至肿瘤科并接受了替莫唑胺化疗。8个月后患者病情稳定,无肿瘤复发。由于PXA的生物学行为不可预测,因此需要密切随访。