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Central neurocytoma

机译:中枢神经细胞瘤

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摘要

Central neurocytomas (CN) are rare intraventricular tumors with prominent neuronal differentiation. CN commonly arise in the lateral ventricles of young adults who predominantly present with raised intracranial pressure. Few studies have described the clinical, pathological, and radiological features of these tumors, and those that have are typically single case reports. Herein, we report ten patients with CN with variable clinical and pathological features and discuss the management of these tumors. Nine tumors occupied the lateral ventricle and only one was located in the sellar region. On MRI, all 10 tumors showed heterogeneous hypo-or iso-intensity on T1-weighted and hyperintensity on T2-weighted MRI. Contrast enhancement varied greatly from very slight to intense. All patients were surgically treated by macroscopic total or subtotal removal. Postoperative radiotherapy was given to six patients (four of whom had undergone subtotal resection and two of whom had undergone total resection). The surgical and histopathological data of these patients were reviewed and analyzed. No recurrences were noted although we were unable to contact two patients for follow-up. A brief review of the literature concerning differential diagnosis and therapeutic aspects of these tumors is also presented.
机译:中枢神经细胞瘤(CN)是罕见的脑室内肿瘤,具有明显的神经元分化。 CN通常出现在主要表现为颅内压升高的年轻人的侧脑室中。很少有研究描述这些肿瘤的临床,病理和放射学特征,而那些通常是单例报告。本文中,我们报告了10例具有可变临床和病理特征的CN患者,并讨论了这些肿瘤的治疗方法。 9个肿瘤占据了侧脑室,只有一个位于鞍区。在MRI上,所有10个肿瘤在T1加权MRI上均显示出异质性低或等强度,在T2加权MRI上显示高强度。对比度增强从非常轻微到强烈变化很大。所有患者均接受了宏观或整体切除术的手术治疗。六名患者接受了术后放疗(其中四名接受了大体切除术,其中两名接受了全切除术)。这些患者的手术和组织病理学数据进行了审查和分析。尽管我们无法联系两名患者进行随访,但未发现复发。还介绍了有关这些肿瘤的鉴别诊断和治疗方面的文献的简要综述。

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