[Secondary myelodysplastic syndrome in a boy with non-Hodgkin's lymphoma].

Q4 Medicine Cesko-Slovenska Pediatrie Pub Date : 1993-11-01
H Hrstková, V Cíhalová, M Pejchlová, M Vrba
{"title":"[Secondary myelodysplastic syndrome in a boy with non-Hodgkin's lymphoma].","authors":"H Hrstková,&nbsp;V Cíhalová,&nbsp;M Pejchlová,&nbsp;M Vrba","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The authors describe the case-history of a boy with secondary myelodysplastic syndrome (MDS) which developed into acute leukaemia. The latter was quite resistant to treatment. The disease was preceded by treatment of NH lymphoma with a high grade of malignity by radiotherapy and chemotherapy. The authors give the total doses of all cytostatics which were administered to the patient. One year prior to diagnosis of MDS cytogenetic examination of peripheral blood revealed a highly pathological karyotype, from the numerical and structural aspect. Among others monosomy of chromosome no. 5 was found which is typical for MDS and these changes indicate as a rule a poor prognosis and relatively early transformation to acute leukaemia.</p>","PeriodicalId":39741,"journal":{"name":"Cesko-Slovenska Pediatrie","volume":"48 11","pages":"641-4"},"PeriodicalIF":0.0000,"publicationDate":"1993-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cesko-Slovenska Pediatrie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The authors describe the case-history of a boy with secondary myelodysplastic syndrome (MDS) which developed into acute leukaemia. The latter was quite resistant to treatment. The disease was preceded by treatment of NH lymphoma with a high grade of malignity by radiotherapy and chemotherapy. The authors give the total doses of all cytostatics which were administered to the patient. One year prior to diagnosis of MDS cytogenetic examination of peripheral blood revealed a highly pathological karyotype, from the numerical and structural aspect. Among others monosomy of chromosome no. 5 was found which is typical for MDS and these changes indicate as a rule a poor prognosis and relatively early transformation to acute leukaemia.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[非霍奇金淋巴瘤男孩继发性骨髓增生异常综合征]。
作者描述了一个男孩继发性骨髓增生异常综合征(MDS)发展成急性白血病的病例史。后者对治疗很有抵抗力。该疾病之前曾接受过高恶性程度的NH淋巴瘤放疗和化疗。作者给出了给病人的所有细胞抑制剂的总剂量。MDS诊断前一年的外周血细胞遗传学检查显示,从数量和结构方面高度病理核型。其中第1号染色体单体。5被发现,这是MDS的典型特征,这些变化通常表明预后较差,较早转化为急性白血病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Cesko-Slovenska Pediatrie
Cesko-Slovenska Pediatrie Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.30
自引率
0.00%
发文量
32
期刊介绍: So stúpajúcou prevalenciou exogénnej obezity v detskom veku je pozorovaný i čoraz častejší výskyt zmien v lipidovom a sacharidovom metabolizme. Ich mediátorom je inzulínová reziste...
期刊最新文献
Prevention in paediatrics New therapies in cystic fibrosis Heart murmur in children The effect of restrictions associated with the covid-19 disease on the prevalence of overweight and obesity in Czech children Cystic fibrosis-related diabetes
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1