来自匹配的非亲属供体(MUD)的造血干细胞移植(HSCT)在使用清髓方案的患有MDS的儿科患者中的成功:来自印度西部的病例报告。

I. Madabhavi, Gaurang Modi, Sandip Shah, A. Patel, A. Anand, H. Panchal, S. Parikh
{"title":"来自匹配的非亲属供体(MUD)的造血干细胞移植(HSCT)在使用清髓方案的患有MDS的儿科患者中的成功:来自印度西部的病例报告。","authors":"I. Madabhavi, Gaurang Modi, Sandip Shah, A. Patel, A. Anand, H. Panchal, S. Parikh","doi":"10.14800/SCTI.738","DOIUrl":null,"url":null,"abstract":"Myelodysplastic syndrome (MDS) is heterogeneous hematopoietic stem cell disorders characterized by ineffective erythropoiesis and dyserythropoiesis. Allogenic HSCT from siblings in our country in pediatric MDS is very well documented. But HSCT from matched unrelated donor (MUD) in paediatric age is still a new concept to implement in our country. We are here presenting the relapse case of MDS (myelodysplastic syndrome) and we had done successful HSCT from MUD in a 14 year old paediatric patient. Myeloablative regimen (fludarabine, busulfan, cyclophosphamide, ATG) was used during HSCT. 100% donor chimerism was found on +day 34 VNTR study. Patient is doing well 1year after HSCT without any complications.","PeriodicalId":90974,"journal":{"name":"Stem cell and translational investigation","volume":"2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2015-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Successful Hematopoietic stem cell transplantation (HSCT) from matched unrelated donor (MUD) in a pediatric patient using myeloablative regimen suffering from MDS: case report from western India.\",\"authors\":\"I. Madabhavi, Gaurang Modi, Sandip Shah, A. Patel, A. Anand, H. Panchal, S. Parikh\",\"doi\":\"10.14800/SCTI.738\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Myelodysplastic syndrome (MDS) is heterogeneous hematopoietic stem cell disorders characterized by ineffective erythropoiesis and dyserythropoiesis. Allogenic HSCT from siblings in our country in pediatric MDS is very well documented. But HSCT from matched unrelated donor (MUD) in paediatric age is still a new concept to implement in our country. We are here presenting the relapse case of MDS (myelodysplastic syndrome) and we had done successful HSCT from MUD in a 14 year old paediatric patient. Myeloablative regimen (fludarabine, busulfan, cyclophosphamide, ATG) was used during HSCT. 100% donor chimerism was found on +day 34 VNTR study. Patient is doing well 1year after HSCT without any complications.\",\"PeriodicalId\":90974,\"journal\":{\"name\":\"Stem cell and translational investigation\",\"volume\":\"2 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-04-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Stem cell and translational investigation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14800/SCTI.738\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem cell and translational investigation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14800/SCTI.738","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

骨髓增生异常综合征(MDS)是一种异质性造血干细胞疾病,其特征是红细胞生成和红细胞生成功能低下。在我国,来自兄弟姐妹的同种异体造血干细胞移植治疗小儿MDS有很好的文献记载。但在我国,儿童年龄非亲属匹配供体造血干细胞移植仍是一个新概念。我们在这里介绍MDS(骨髓增生异常综合征)复发病例,我们已经成功地对一名14岁的儿科患者进行了MUD的HSCT。HSCT期间使用清髓方案(氟达拉滨、丁硫凡、环磷酰胺、ATG)。在第34天的VNTR研究中发现100%的供体嵌合。患者移植后1年情况良好,无任何并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Successful Hematopoietic stem cell transplantation (HSCT) from matched unrelated donor (MUD) in a pediatric patient using myeloablative regimen suffering from MDS: case report from western India.
Myelodysplastic syndrome (MDS) is heterogeneous hematopoietic stem cell disorders characterized by ineffective erythropoiesis and dyserythropoiesis. Allogenic HSCT from siblings in our country in pediatric MDS is very well documented. But HSCT from matched unrelated donor (MUD) in paediatric age is still a new concept to implement in our country. We are here presenting the relapse case of MDS (myelodysplastic syndrome) and we had done successful HSCT from MUD in a 14 year old paediatric patient. Myeloablative regimen (fludarabine, busulfan, cyclophosphamide, ATG) was used during HSCT. 100% donor chimerism was found on +day 34 VNTR study. Patient is doing well 1year after HSCT without any complications.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信