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儿童脑实质巨大脉络丛乳头状瘤术后复发1例及文献复习
作者:张瑞1  王新法1  高修成2  钱静1  郑雷1  祝永杰1  王刚1  何俊平1 
单位:1. 南京医科大学附属儿童医院 神经外科, 江苏 南京 210029;
2. 南京医科大学附属儿童医院 影像科, 江苏 南京 210029
关键词:脉络丛乳头状瘤 脑室外 复发 
分类号:R739.41
出版年·卷·期(页码):2017·36·第四期(547-550)
摘要:

目的:探讨脑室外脉络丛乳头状瘤的临床表现、影像病理学特征及治疗预后。方法:回顾性分析1例发生于脑实质的脉络丛乳头状瘤患儿的临床资料及复习相关文献。结果:患儿肿瘤组织起源于脑实质,病理学结果证实为脉络丛乳头状瘤。结论:脑室外脉络丛乳头状瘤为中枢神经系统少见良性肿瘤,复发率极低,明确诊断须行组织病理学检查,手术全切是其主要治疗手段。

Objective:To explore the clinical manifestation, radiological and histopathological characteristics, treatment and prognosis of extraventricular choroid plexus papilloma. Methods:Data including clinical manifestations, imaging features, histopathological characteristics and treatment strategies were analyzed in a cerebral parenchymal choroid plexus papilloma case followed by literature review. Results:The lesion in the three-year-old boy originated in the cerebral parenchymal areas was indentified as choroid plexus papilloma via histopathological tests. Conclusion:Extraventricular choroid plexus papilloma is a rare benign tumor of central nervous system,whose recurrence is extremely rare. The diagnosis mainly depends on histopathological findings. The preferred treatment of these lesions is gross total resection.

参考文献:

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[8] NOMURA H,MOMMA F,FURUICHI S,et al.Primary choroid plexus papilloma of the foramen magnum-case report[J].Neurol Med Chir (Tokyo),1997,37(9):685-687.
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