松细胞瘤:赫尔辛基神经外科四例病例的长期随访研究

J. Choque-Velasquez, Julio C. Resendiz-Nieves, B. R. Jahromi, R. Colasanti, R. Raj, O. Tynninen, M. Niemelä, J. Hernesniemi
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引用次数: 1

摘要

背景:松细胞瘤是一种罕见的良性病变,如果可以实现全切除,预后相对较好。病例报告:我们对1997年后连续手术的4例经组织学证实的松果体细胞瘤患者进行了回顾性分析。我们所有患者的平均随访时间为224,5个月(204-246个月)。所有病例均完成了大体全切除。报道了手术切除松果体细胞瘤的基石。结论:在对松果体病变进行全显微外科大体切除的基础上,对松果体细胞瘤进行适当的治疗,可以获得良好的长期疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pineocytomas: a long-term follow up study of four cases in Helsinki Neurosurgery
Background: Pineocytomas are rare benign lesions with a relatively good prognosis if gross total resection can be achieved. Report of cases: We present a retrospective review of four patients with histologically confirmed pineocytomas consecutively operated on after 1997. All of our patients were alive at a mean follow-up of 224,5 months (range 204-246). A gross total resection was accomplished in all cases. The cornerstones for the surgical resection of pineocytomas are reported. Conclusions: A proper management of pineocytomas, based on the gross total microsurgical resection of the lesion, results in an excellent long term outcome of these pineal lesions.
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