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[原发性血小板增多症中的血小板体积]

[Platelet volume in essential thrombopenia].

作者信息

Le Tohic F, Prost-Dvojakovic R J, Le Menn R, Samama M

出版信息

Nouv Rev Fr Hematol (1978). 1978 Jun 10;20(2):155-71.

PMID:568255
Abstract

The electronic method for measuring platelet volume using the Coulter Z BI Counter coupled with a Channelyser C 1000 has been standardized. The distribution of platelet volumes was studied in 28 cases of idiopathic thrombocytopenic purpura (ITP) and in 59 cases of thrombocytopenia attributed to a failure of platelet production. Results showed that the volumetric distribution curve of platelet rich plasma (PRP) was altered in 40 cases, by the presence of small particles interfering with platelets of small volume and/or by residual red cells modifying its terminal segment. These abnormalities seem linked to the degree of thrombopenia, but independent of its central or peripheral origin. A method of isolation and concentration of platelets in an albumin gradient allowed the restoration of the classical volume distribution in 24 cases out of 40. Simulated thrombopenias obtained by dilution of platelets in their own platelet poor plasma (PPP) showed that the abnormalities in the small volume range could be reproduced in vitro by modifying the proportion of platelets and of small residual elements in the PRP. When the albumin gradient method was used, the classical distribution of platelet volumes was found. Preliminary electron-microscopy studies show that the small elements in the PRP of thrombopenic subjects could be formed by red cell fragments. Cytoenzymologic studies should be able to confirm this. Volumetric parameters were determined from the asymmetric and unimodual distribution of platelets, either directly on PRP or after concentration and separation of platelets in an albumin gradient. They showed that platelet volumes were very often increased in ITP but also occasionnally in thrombopenia of attributed to a failure of production.

摘要

使用库尔特Z BI计数器与通道分析仪C 1000联用测量血小板体积的电子方法已实现标准化。对28例特发性血小板减少性紫癜(ITP)患者和59例因血小板生成障碍导致血小板减少的患者的血小板体积分布进行了研究。结果显示,40例患者富含血小板血浆(PRP)的体积分布曲线发生改变,原因是存在干扰小体积血小板的小颗粒和/或残留红细胞改变了其末端部分。这些异常似乎与血小板减少的程度有关,但与血小板减少是中枢性还是外周性起源无关。一种在白蛋白梯度中分离和浓缩血小板的方法使40例中的24例恢复了经典的体积分布。通过在自身乏血小板血浆(PPP)中稀释血小板获得的模拟血小板减少症表明,通过改变PRP中血小板和小残留成分的比例,可以在体外重现小体积范围内的异常情况。当使用白蛋白梯度方法时,发现了血小板体积的经典分布。初步电子显微镜研究表明,血小板减少患者PRP中的小成分可能由红细胞碎片形成。细胞酶学研究应该能够证实这一点。血小板体积参数是根据血小板的不对称单峰分布直接在PRP上或在白蛋白梯度中对血小板进行浓缩和分离后确定的。结果表明,ITP患者的血小板体积常常增大,但在因生成障碍导致的血小板减少症中也偶尔会增大。

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