Erslev A J, Palascak J E, Shaikh B S, Martinez J
Cardeza Foundation for Hematologic Research, Jefferson Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
J Lab Clin Med. 1998 Jun;131(6):488-95; discussion 487. doi: 10.1016/s0022-2143(98)90056-7.
A family with autosomal dominant macrothrombocytopenia is described. Despite severe thrombocytopenia, only a moderate hemorrhagic tendency was observed. Kinetic studies revealed a normal platelet survival, normal megakaryocytic numbers, and normal bone marrow responsiveness. The rate of platelet production was set low, despite moderately impaired hemostasis and thrombocytopenia; it apparently was set to maintain another platelet parameter at an optimal level. Measurements of total circulating platelet mass and platelet surface suggested that the platelet production was set to maintain the platelet surface rather than the platelet mass at a normal value.
本文描述了一个常染色体显性遗传性大血小板减少症家族。尽管存在严重的血小板减少,但仅观察到中度出血倾向。动力学研究显示血小板生存期正常、巨核细胞数量正常以及骨髓反应正常。尽管止血功能中度受损且存在血小板减少症,但血小板生成速率设定较低;显然这是为了将另一个血小板参数维持在最佳水平。对总循环血小板量和血小板表面的测量表明,血小板生成设定为将血小板表面而非血小板量维持在正常水平。