儿童Ewing肉瘤脑内转移的手术治疗。病例报告及复查]。

Q4 Medicine

Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko Pub Date : 2025-01-01 DOI:10.17116/neiro20258902192

A V Sanakoeva, A E Samarin, E I Konopleva, A V Tarakanova, I V Sidorov, A E Druy, A I Karachunsky

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引用次数: 0

摘要

背景：儿童尤文氏肉瘤继发于骨骼和软组织的转移性脑病变极为罕见，且预后不良。很少有出版物专门讨论这个问题。开颅手术后的存活率极低。作者描述了一个患者转移形式的尤文氏肉瘤和两个脑内（幕上和幕下）转移。全切除后放疗和化疗，病情稳定缓解23个月。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

[Surgical treatment of intracerebral metastases of Ewing sarcoma in children. Case report and review].

Background: Metastatic brain lesions following Ewing sarcoma of bones and soft tissues in children are extremely rare and have unfavorable prognosis. There are few publications devoted to this issue. Survival rates after craniotomy are extremely low.

The authors describe a patient with metastatic form of Ewing sarcoma and two intracerebral (supra- and infratentorial) metastases. Total resection with subsequent radio- and chemotherapy were followed by stable remission for 23 months.

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来源期刊

Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko Medicine-Neurology (clinical)

CiteScore

0.70

自引率

0.00%

发文量

期刊介绍： Scientific and practical peer-reviewed journal. This publication covers the theoretical, practical and organizational problems of modern neurosurgery, the latest advances in the treatment of various diseases of the central and peripheral nervous system. Founded in 1937. English version of the journal translates from Russian version since #1/2013.