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非典型乳头状胶质神经元肿瘤。

Atypical papillary glioneuronal tumor.

作者信息

Vaquero Jesús, Coca Santiago

机构信息

Department of Neurosurgery, Puerta de Hierro Hospital, Autonomous University, San Martin de Porres, 4, Madrid 28035, Spain.

出版信息

J Neurooncol. 2007 Jul;83(3):319-23. doi: 10.1007/s11060-007-9333-3. Epub 2007 Feb 7.

Abstract

We describe a 34-year-old man who presented with headaches for about 3 months. Magnetic Resonance Imaging (MRI) revealed a large cystic tumor, involving the right frontoparietal lobe region. Pathological study revealed a papillary glioneuronal tumor (PGNT) with mitotic activity and a Ki-67 labeling index of approximately 15%. Five years after radical surgery and radiotherapy, the patient is symptom-free, without tumor recurrence or residual tumor. This case supports the existence of an atypical variant of PGNT, with mitotic activity and high proliferative index, and suggests that in these tumors, histological findings of malignity not necessarily indicate a short-term unfavorable behavior.

摘要

我们描述了一名34岁男性,他出现头痛症状约3个月。磁共振成像(MRI)显示一个巨大的囊性肿瘤,累及右侧额顶叶区域。病理研究显示为具有有丝分裂活性且Ki-67标记指数约为15%的乳头状胶质神经元肿瘤(PGNT)。根治性手术和放疗五年后,患者无症状,无肿瘤复发或残留肿瘤。该病例支持存在具有有丝分裂活性和高增殖指数的PGNT非典型变体,并表明在这些肿瘤中,恶性的组织学表现不一定预示短期不良行为。

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