两名患有先天性红细胞生成异常性贫血II型（CDA-II）并伴有铁过载的脾切除兄弟姐妹出现帕彭海默小体（含铁红细胞）过多。
Excess of Pappenheimer bodies (siderocytes) in two splenectomized siblings with congenital dyserythropoietic anemia--type II (CDA-II) and iron overload.
作者信息
Chrobák Ladislav, Matysová Jindriska
机构信息
Charles University in Prague, Faculty of Medicine and University Hospital in Hradec Králové: 2nd Department of Medicine, Division of Clinical Hematology.
出版信息
Acta Medica (Hradec Kralove). 2004;47(3):187-8.
PMID:15568737
Abstract
In two splenectomized siblings with congenital dyserythropoietic anemia type-II (CDA-II) and iron overload excess of Pappenheimer bodies reaching 46.4% and 15.9% respectively was found. Cause, significance and differential diagnosis of this finding were discussed.
摘要
在两名患有II型先天性红细胞生成异常性贫血（CDA-II）的脾切除同胞中，发现帕彭海默小体过多，铁过载分别达到46.4%和15.9%。讨论了这一发现的原因、意义及鉴别诊断。
Zotero 插件