期刊文献+
共找到1篇文章
< 1 >
每页显示 20 50 100
唐氏综合征新生儿患者的一过性骨髓增生综合征:对来自AML-BFM和ESPED研究项目的115例患儿的综述和分析
1
作者 diekamp s. Creutzig U. +2 位作者 Reinhardt D. Baumann-Khler M. 唐彦 《世界核心医学期刊文摘(儿科学分册)》 2006年第8期55-55,共1页
Transient myeloproliferative syndrome(TMS)is a disorder of neonates with Dow n syndrome(trisomy 21)and occurs at an incidence of up to 10%.Typical for th is entity is a proliferation of myeloid blasts with megakaryobl... Transient myeloproliferative syndrome(TMS)is a disorder of neonates with Dow n syndrome(trisomy 21)and occurs at an incidence of up to 10%.Typical for th is entity is a proliferation of myeloid blasts with megakaryoblastic and/or eryt hroblastic features detectable in the peripheral blood.In the majority of cases TMS is asymptomatic,and only a small percentage of children show clinical symp toms due to hyperleukocytosis,thrombocytopenia,anemia,or hepatomegaly.Almost all children will achieve spontaneous remission after 2-4 months(disappearanc e of myeloid blasts and regression of clinical symptoms).Patients with initial hyperleukocytosis and hepatomegaly,however,carry a particular risk of developi ng hepatopathy followed frequently by lethal liver fibrosis.Chemotherapy with c ytarabine is indicated in patients with clinical symptoms of hyperleukocytosis o r early signs of hepatopathy.Within the first 4 years the risk of developing ac ute myeloblastic leukemia(AML)is high at 20-30%;therefore,regular followup s are advised.This analysis is based on one of the largest databases for TMS. 展开更多
关键词 骨髓增生综合征 新生儿患者 唐氏综合征 一过性 患儿 AML 白细胞增多 21三体综合征 粒细胞性白血病 项目
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部