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原发性血小板增多症

Essential thrombocythaemia.

作者信息

Woodruff R K, Bell W R, Castaldi P A, Streatfield K, Penington D G

出版信息

Haemostasis. 1980;9(2):105-25. doi: 10.1159/000214347.

Abstract

The results of detailed studies of 3 patients with essential thrombocythaemia (ET) are presented. Qualitative tests of platelet function were abnormal, and autologous platelet survivals were diminished. Megakaryocyte ploidy distribution analysis showed an increased proporttion of cells with high ploidy, and buoyant density distribution analysis showed increased proportions of less dense platelets. Ultrastructural studies of the platelets showed proliferation of the dense tubular system with deficiency of the surface-connected canalicular system. Megakaryocyte electron microscopy showed abnormal distribution of demarcation membrane complex and granules. The precise functional abnormality of the platelets in ET has not yet been defined, but a release defect of variable severity with corresponding morphological abnormalities of dense tubular and surface-connected canalicular systems, seems the most likely explanation.

摘要

本文展示了对3例原发性血小板增多症(ET)患者的详细研究结果。血小板功能的定性测试异常,自体血小板存活期缩短。巨核细胞倍性分布分析显示高倍性细胞比例增加,浮力密度分布分析显示低密度血小板比例增加。血小板的超微结构研究显示致密管状系统增殖,表面连接小管系统缺乏。巨核细胞电子显微镜检查显示分界膜复合物和颗粒分布异常。ET中血小板的确切功能异常尚未明确,但最可能的解释似乎是程度不一的释放缺陷以及致密管状和表面连接小管系统相应的形态学异常。

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