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神经母细胞瘤转化为节细胞神经瘤的临床观察
引用本文:李穗生,刘唐彬,周慕珩. 神经母细胞瘤转化为节细胞神经瘤的临床观察[J]. 中华小儿外科杂志, 2001, 22(6): 341-342
作者姓名:李穗生  刘唐彬  周慕珩
作者单位:1. 中山医科大学附属第一医院小儿外科
2. 中山医科大学病理教研室
摘    要:目的:了解神经母细胞瘤转化为良性的节细胞神经瘤的规律,总结经验,提出治疗方法。方法:回顾1981年1月-1998年12月我院收治103例神经母细胞瘤中3例转化为节细胞神经瘤的治疗经过及组织学变化。结果:3例患儿至今生存,分别经过2次以上手术,采用多药联合的强化化疗。组织学已改变成为节细胞神经瘤。结论:对神经母细胞瘤的治疗应 积极,尤其对那些第一次手术不能完整切除肿瘤的患儿更应如此。对带瘤生长时间长,生活质量好的病例应高度怀疑肿瘤有转化为良性肿瘤的可能。

关 键 词:神经母细胞瘤 细胞转化 肿瘤 节细胞神经瘤 小儿
修稿时间:2000-04-29

Clinical study on neuroblastoma transforming into ganglioneuroma
LI Suisheng,LIU Tangbin,ZHOU Muheng. Clinical study on neuroblastoma transforming into ganglioneuroma[J]. Chinese Journal of Pediatric Surgery, 2001, 22(6): 341-342
Authors:LI Suisheng  LIU Tangbin  ZHOU Muheng
Affiliation:LI Suisheng,LIU Tangbin,ZHOU Muheng.Department of Pediatric Surgery,The First Affiliated Hospital of Sun Yat-Sen University of Medical Sciences,Guangzhou 510080,China
Abstract:Objective To identify the pattern of neuroblastoma transforming into ganglioneuroma and find the treatment for the condition.Methods The histological changes and course of treatment were reviewed on 3 patients who had experienced tumor transformation. They were among 103 neuroblastoma patients admitted from 1981.1 to 1998.12.Results Three patients have all survived and received operations for over two times. Combined intensive chemical therapy was employed on them. Histological study showed change to ganglioneuroma.Conclusions Aggressive treatment should be adopted, especially for children in whom the complete removal of tumor can not be achieved by the first operation. For patients who had long tumor-loaded survival and good life quality, the possibility of neuroblastoma transforming into ganalioneuroma should be suspected.
Keywords:Neuroblastoma  Cell transformation  neoplastic  Neoplasms by histologic type
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