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A case report of high-grade astroblastoma in a young adult

机译:青年人高级星形母细胞瘤1例

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Astroblastoma is an uncommon neuroepithelial primary tumor of the brain which is of uncertain origin. We present a case of high-grade astroblastoma in an 18-year-old female with a severe headache, loss of appetite, vomiting and generalized weakness. The patient had undergone a right frontoparietal craniotomy. Large subfalcine meningioma was excised. The lesion was suspected to be a meningioma. Primary radiological investigation revealed a 6.8?cm?×?5.8?cm?×?5.4?cm lesion. Although the radiological and intraoperative findings were of an extra-axial tumor, the histology and immunophenotype was of an astroblastoma. The patient was treated with cyclophosphamide, cisplatin and etoposide chemotherapy regimen. The patient was later treated with bi-weekly bevacizumab. The patient had improved symptomatically post-chemotherapy. However, there was no significant difference in lesion size. The patient died after 2 weeks. The prognosis of patients with astroblastoma is extremely poor as observed in our case.
机译:星形母细胞瘤是一种罕见的大脑神经上皮原发性肿瘤,来源不明。我们在一名严重头痛,食欲不振,呕吐和全身无力的18岁女性中出现一例高级星形母细胞瘤。该患者已进行了一次右前额开颅手术。切除了大的亚足膜下脑膜瘤。病变被怀疑是脑膜瘤。初步放射学检查发现病变为6.8?cm?×?5.8?cm?×?5.4?cm。尽管放射学和术中发现是轴外肿瘤,但组织学和免疫表型是星形母细胞瘤。该患者接受了环磷酰胺,顺铂和依托泊苷化疗方案的治疗。该患者随后每两周接受一次贝伐单抗治疗。患者在化学疗法后对症改善。但是,病变大小无明显差异。该患者在2周后死亡。如本例所述,星形母细胞瘤患者的预后极差。

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