Tang W, Cai S P, Eng B, Poon M C, Waye J S, Illum N, Chui D H
Department of Pathology, McMaster University, School of Medicine, Hamilton, Ontario, Canada.
Blood. 1993 Mar 15;81(6):1636-40.
A 10-year-old Danish girl with congenital anemia is described. At birth, she had severe anemia and erythroblastosis and was transfused a number of times during the first year. The need for transfusions has since declined steadily. Her reticulocyte counts varied between 2% and 15%, and her bone marrow aspirate showed some dyserythropoietic features. Her hemoglobin F level was consistently elevated, up to as much as 41%. Her erythrocytes had a normal level of I antigen but an undetectable level of i antigen. Moreover, embryonic zeta-globin and epsilon-globin chains were present in some of her circulating erythrocytes. These findings may represent the manifestations of a new variant of congenital anemia.
本文描述了一名患有先天性贫血的10岁丹麦女孩。出生时,她患有严重贫血和红细胞增多症,并在第一年接受了多次输血。此后输血需求稳步下降。她的网织红细胞计数在2%至15%之间波动,骨髓穿刺显示有一些红细胞生成异常的特征。她的血红蛋白F水平持续升高,高达41%。她的红细胞I抗原水平正常,但i抗原水平检测不到。此外,她的一些循环红细胞中存在胚胎ζ-珠蛋白和ε-珠蛋白链。这些发现可能代表了一种先天性贫血新变体的表现。