Suppr超能文献

难治性骨髓增生异常综合征长期存活者的临床特征。一项日本合作研究。

Clinical features of long-term survivors of refractory myelodysplastic anemias. A Japanese cooperative study.

作者信息

Yoshida Y, Oguma S, Uchino H, Maekawa T, Nomura T

机构信息

Department of Medicine, Faculty of Medicine, Kyoto University, Japan.

出版信息

Leuk Res. 1992 Aug;16(8):775-9. doi: 10.1016/0145-2126(92)90156-2.

Abstract

Eighty-one of 473 patients with refractory myelodysplastic anemias registered by the Japanese Cooperative Study Group prior to January 1987 survived more than 5 years. At presentation, most patients had mild cytopenia, a less aggressive form of the disease (48 with refractory anemia, 23 with refractory anemia with ring sideroblasts, 10 with refractory anemia with excess of blasts), less blast cells in the marrow and blood, and onset at younger ages. Their clinical profiles 5 years after presentation showed no significant improvement. The results suggest that the long-term survivors were found in a subpopulation of patients with a favorable prognosis and that it is a part of the natural course rather than the results of treatment.

摘要

在1987年1月之前由日本合作研究组登记的473例难治性骨髓增生异常综合征贫血患者中,81例存活超过5年。就诊时,大多数患者有轻度血细胞减少,疾病侵袭性较低(48例难治性贫血,23例伴有环形铁粒幼细胞的难治性贫血,10例伴有过多原始细胞的难治性贫血),骨髓和血液中的原始细胞较少,且发病年龄较轻。就诊5年后他们的临床特征无显著改善。结果表明,长期存活者见于预后良好的患者亚群中,这是自然病程的一部分而非治疗结果。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验