Matsumoto N, Ishihara T, Takahashi M, Uchino F, Ono J
Acta Pathol Jpn. 1976 Sep;26(5):533-42. doi: 10.1111/j.1440-1827.1976.tb00510.x.
Light and electron microscopic studies of the spleen and liver from a patient with hereditary elliptocytosis have been reported. Characteristic findings are congestion of the cordal space, diminished variation of the erythrocyte shape in the cord, relatively empty sinuses and erythrophagocytosis by the cordal macrophages. The same basic defect of the red cell membrane as has been documented in hereditary sperocytosis might be a possible explanation on the pathogenesis of this rare hemolytic anemia.
已有报道对一名遗传性椭圆形红细胞增多症患者的脾脏和肝脏进行了光镜和电镜研究。特征性发现包括脾索间隙充血、脾索内红细胞形状变化减少、脾窦相对空虚以及脾索巨噬细胞的红细胞吞噬现象。与遗传性球形红细胞增多症中所记录的相同的红细胞膜基本缺陷可能是这种罕见溶血性贫血发病机制的一种可能解释。
