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  

Recurrence of giant cerebral parenchymal choroid plexus papilloma: a case report and literature review

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] 

机构地区：[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

出　　处：《东南大学学报（医学版）》2017年第4期547-550,共4页Journal of Southeast University(Medical Science Edition)

基　　金：国家自然科学基金资助项目(81602212);江苏省自然科学基金资助项目(BK20161119);南京市医学科技发展基金资助项目(YKK15139);南京医科大学科技发展基金资助项目(2014NJMUZD080)

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.

关 键 词：脉络丛乳头状瘤 脑室外 复发 

分 类 号：R739.41[医药卫生—肿瘤]