论文部分内容阅读
我院1988年3月至1992年11月对15例骨髓异常增生综合征,MDS演变进行初步临床观察,现报告如下。 1 临床资料:①一般资料:15例MDS男9例,女6例。年龄16岁—72岁。②诊断按FAB协作组《关于骨髓增生异常综合征的分类建议》。MDS类型:难治性贫血(RA)12例,原发性铁粒幼红细胞难治性贫血(RAS)1例,原始细胞过多性难治性贫血(RAEB)1例,转化型原始细胞过多性难治性贫血(RAEB—T)1例。③定状与体征:贫血15例。11例鼻衄、齿龈出血、皮肤粘膜出
Our hospital from March 1988 to November 1992 on 15 cases of myelodysplastic syndrome, MDS evolution of the initial clinical observations are as follows. 1 Clinical data: ① General Information: 15 cases of MDS male 9 cases, 6 females. Age 16 years old - 72 years old. ② diagnosis by FAB collaboration group “on the classification of myelodysplastic syndrome suggestion.” MDS type: refractory anemia (RA) in 12 cases, primary iron refractory anemia (RAS) in 1 case, primitive refractory anemia (RAEB) in 1 case, transformed primitive cells 1 case of multiple refractory anemia (RAEB-T). ③ shape and signs: anemia in 15 cases. 11 cases of epistaxis, gum bleeding, skin and mucous membranes out