Mutoh S, Sasaki R, Takaku F, Aoyama M, Moriyama S, Yoshimoto M, Yawata Y
Am J Hematol. 1983 Apr;14(2):113-20. doi: 10.1002/ajh.2830140203.
A rare familial case of hereditary stomatocytosis with hemolytic anemia, increased autohemolysis, increased osmotic fragility, and shortened erythrocyte survival is described. The erythrocytes were abnormally permeable to sodium and potassium. In addition, "Na-K pump" rate of the red blood cells was increased, while Na+-K+-ATPase, Mg2+-ATPase and Mg2+-Ca2+-ATPase activities were within normal limits. Splenectomy induced marked improvement of anemia.
描述了一例罕见的家族性遗传性口形红细胞增多症病例,伴有溶血性贫血、自身溶血增加、渗透脆性增加和红细胞存活期缩短。红细胞对钠和钾的通透性异常。此外,红细胞的“钠-钾泵”速率增加,而钠钾ATP酶、镁ATP酶和镁钙ATP酶活性在正常范围内。脾切除术后贫血明显改善。