非婴儿期结缔组织增生神经节胶质瘤的长期随访。

Central European Neurosurgery Pub Date : 2010-02-01 Epub Date: 2009-12-18 DOI:10.1055/s-0029-1241180
K Nanassis, P P Tsitsopoulos, D Marinopoulos, I Venizelos, P D Tsitsopoulos
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引用次数: 4

摘要

结缔组织增殖性神经节胶质瘤是一种混合性脑肿瘤,传统上报道发生于婴儿。然而,一些非婴儿病例已被记录。我们报告一个16岁男性的结缔组织增生神经节胶质瘤病例。病人说头疼得厉害。影像学检查显示右侧额叶有一个大肿块。病灶被完全切除。组织病理学检查证实了结缔组织增生神经节胶质瘤的诊断。术后过程良好。10(1/2)年随访未见肿瘤复发。虽然结缔组织增殖性神经节胶质瘤具有侵袭性特征,完全手术切除是治疗的选择,避免了辅助治疗的需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term follow-up of a non-infantile desmoplastic ganglioglioma.

Desmoplastic gangliogliomas are mixed cerebral tumors traditionally reported in infants. However, a few non-infantile cases have been documented. A case of a desmoplastic ganglioglioma in a 16-year male is presented. The patient reported severe headaches. Radiological examination revealed a large mass occupying the right frontal lobe. The lesion was totally excised. Histopathological examination confirmed the diagnosis of a desmoplastic ganglioglioma. The postoperative course was excellent. At the 10(1/2) year follow-up there was no evidence of tumor recurrence. Although desmoplastic gangliogliomas have aggressive features, complete surgical removal is the treatment of choice obviating the need for adjuvant therapy.

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Central European Neurosurgery
Central European Neurosurgery CLINICAL NEUROLOGY-NEUROSCIENCES
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