Myelodysplastic syndrome terminating in erythropoietic protoporphyria after 15 years of aplastic anemia

被引：0
|
作者：
Shirota, T [1 ]
Yamamoto, H [1 ]
Hayashi, S [1 ]
Fujimoto, H [1 ]
Harada, Y [1 ]
Hayashi, T [1 ]
机构：
[1] Tokyo Med Univ, Dept Internal Med 3, Shinjuku Ku, Tokyo, Japan
来源：
INTERNATIONAL JOURNAL OF HEMATOLOGY | 2000年 / 72卷 / 01期
关键词：
myelodysplastic syndrome; aplastic anemia; erythropoietic protoporphyria;
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
The authors report a case of aplastic anemia in which refractory anemia, a subtype of myelodysplastic syndrome (MDS), developed 15 years after the onset and was subsequently followed by erythropoietic protoporphyria (EPP). Defects of stem cells in MDS are thought to be responsible for the disturbance of the heme biosynthetic pathway leading to the development of EPP. Int J Hematol. 2000;71:44-47. (C) 2000 The Japanese Society of Hematology.
引用
收藏
页码：44 / 47
页数：4
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