双颅内原发性:罕见

Aastha Shah, M. Patel, U. Suryanarayan
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引用次数: 0

摘要

两种或两种以上不同细胞类型颅内恶性肿瘤的发生率极为罕见,在所有原发性中枢神经系统肿瘤中的发病率<0.9%。在此,我们报告一例罕见的垂体大腺瘤合并多形性胶质母细胞瘤,高度侵袭性恶性肿瘤,33岁男性,最初主诉为间歇性头痛和呕吐。临床表现,放射学特征,并接受治疗的病人简要讨论,并回顾文献。患者接受手术、放化疗和内科治疗。放疗后,脑增强计算机断层扫描显示垂体病变的分辨率随术后改变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dual intracranial primaries: A rare occurrence
The incidence of two or more intracranial malignancies of different cell types is extremely rare with an incidence of <0.9% of all primary central nervous system tumors. Herein, we report the rare combination of pituitary macroadenoma, benign condition with glioblastoma multiforme, highly aggressive malignancy in a 33-year-old male with the initial complaints of intermittent headache and vomiting. The clinical presentation, radiological characteristics, and treatments received by the patient are briefly discussed along with review of literature. The patient was treated with surgery followed by chemoradiotherapy and medical management. Post radiation, contrast-enhanced computed tomography scan of the brain showed postoperative changes with the resolution of the pituitary lesion.
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