Goebel K M, von Manteuffel G, Hausmann L, Kaffarnik H
Med Klin. 1979 May 4;74(18):691-4.
Heterogeneous clinical features of inherited hemolytic anemia due to pyruvate kinase (PK) deficiency were observed in three related homozygous patients. Erythrocytes were separated into old and young cells by means of density-layer centrifugation using a new supporting medium: Stractan-Urografin gradients. Those fractions containing older RBC disclosed defective PK which resulted in an impaired metabolism. Following an intake of chloramphenicol the clinical course of one female family member converted to acute monocytic leukemia. Thus, the report of a PK instability trait, in one family member associated with pancytopenia which converted in leukemia, suggests that inherited red cell enzyme deficiency might be also an expression of the vulnerability of the hematopoietic stem cells.
在三名相关的纯合子患者中观察到丙酮酸激酶(PK)缺乏所致遗传性溶血性贫血的异质性临床特征。使用一种新的支持介质:Stractan-泛影葡胺梯度,通过密度层离心法将红细胞分为老细胞和年轻细胞。那些含有较老红细胞的组分显示PK缺陷,这导致代谢受损。一名女性家庭成员在摄入氯霉素后临床病程转变为急性单核细胞白血病。因此,一名家庭成员中与全血细胞减少相关且转变为白血病的PK不稳定特征报告表明,遗传性红细胞酶缺乏可能也是造血干细胞易损性的一种表现。