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Papillary meningioma: an aggressive variant meningioma with clinical features and treatment: a retrospective study of 10 cases

机译:乳头状脑膜瘤:具有临床特征和治疗方法的侵袭性变异型脑膜瘤:10例回顾性研究

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Introduction: Papillary meningioma is a rare subtype of malignant meningiomas. The aim of this retrospective study was to investigate the clinical, radiological, histopathological features and prognosis for papillary meningioma at our institutions. Materials and methods: Ten patients with clinically, radiologically and histopathologically confirmed papillary meningiomas were treated at our hospitals. The clinical data, imaging characteristics, histopathological features, surgical treatment and postoperative follow-up, were analyzed retrospectively. Results: The patients with a mean age of 36.9 years at the time of their initial operations. The papillary meningiomas were predominantly located in the convexity (n = 6). At their initial operation, six patients underwent gross total resection and four patients underwent subtotal resection. The mean post-operative follow-up period was 42.6 months (range: 12-90 months). Six patients underwent multiple surgical resections. The mean time to first recurrence was 21.5 months. On magnetic resonance imaging scan, marked enhancements and dural tail signs were displayed in all lesions. All lesions showed peritumoral edema. Cysts were seen in four lesions. Bone hyperostosis or destruction was seen in six lesions. Cerebrospinal fluid dissemination was seen in three lesions. Incomplete surgical resection was associated with recurrence. MIB-1 labeling index was associated with progression-free survival for patients (p = 0.0442). Conclusions: Papillary meningioma has a tendency to present in middle-aged patients, and it has specific clinical and histopathological characteristics. MIB-1 labeling index and the extent of resection might predict the recurrence. Cystic formation, peritumoral edema, osseous change and CSF dissemination might be neuroimaging characteristics of papillary meningioma, especially in recurrence papillary meningioma.
机译:简介:乳头状脑膜瘤是一种罕见的恶性脑膜瘤亚型。这项回顾性研究的目的是调查我们机构中乳头状脑膜瘤的临床,影像学,组织病理学特征和预后。材料和方法:十例经临床,放射学和组织病理学证实为乳头状脑膜瘤的患者在我们医院接受治疗。回顾性分析其临床资料,影像学特征,组织病理学特征,手术治疗和术后随访情况。结果:初次手术时平均年龄为36.9岁的患者。乳头状脑膜瘤主要位于凸面(n = 6)。初次手术时,有6例患者行了全切除,有4例患者进行了大体切除。术后平均随访时间为42.6个月(范围:12-90个月)。六名患者接受了多次手术切除。首次复发的平均时间为21.5个月。在磁共振成像扫描中,所有病变均显示出明显的增强和硬脑膜尾征。所有病变均表现为肿瘤周围水肿。在四个病变中可见囊肿。在六个病变中可见骨肥大或破坏。在三个病变中可见脑脊液扩散。手术切除不完全与复发有关。 MIB-1标记指数与患者的无进展生存期相关(p = 0.0442)。结论:乳头状脑膜瘤倾向于在中年患者中出现,具有特定的临床和组织病理学特征。 MIB-1标记指数和切除范围可预测复发。囊性形成,肿瘤周围水肿,骨性改变和CSF传播可能是乳头状脑膜瘤的神经影像学特征,尤其是在复发性乳头状脑膜瘤中。

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