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急性髓系白血病中的血小板缺陷。

The platelet defect in acute myeloid leukaemia.

作者信息

Woodcock B E, Cooper P C, Brown P R, Pickering C, Winfield D A, Preston F E

出版信息

J Clin Pathol. 1984 Dec;37(12):1339-42. doi: 10.1136/jcp.37.12.1339.

DOI:10.1136/jcp.37.12.1339
PMID:6595273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC499013/
Abstract

In a study of platelets from 13 patients with acute myeloid leukaemia abnormal aggregation and release reactions were found. A previously unrecognised quantitative defect of thromboxane B2 production may, at least in part, explain these findings. In contrast to a previous report, we were unable to show a convincing storage pool defect in these platelets. The platelet membrane glycoproteins were largely normal.

摘要

在一项对13例急性髓细胞白血病患者血小板的研究中,发现了异常的聚集和释放反应。一种先前未被认识的血栓素B2生成的定量缺陷可能至少部分地解释了这些发现。与之前的一份报告相反,我们未能在这些血小板中显示出令人信服的储存池缺陷。血小板膜糖蛋白在很大程度上是正常的。

相似文献

1
The platelet defect in acute myeloid leukaemia.急性髓系白血病中的血小板缺陷。
J Clin Pathol. 1984 Dec;37(12):1339-42. doi: 10.1136/jcp.37.12.1339.
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Blood platelets in cardiopulmonary bypass operations. Recovery occurs after initial stimulation, rather than continual activation.心肺转流手术中的血小板。恢复发生在初始刺激之后,而非持续激活之后。
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Deficiency of (33P)2MeS-ADP binding sites on platelets with secretion defect, normal granule stores and normal thromboxane A2 production. Evidence that ADP potentiates platelet secretion independently of the formation of large platelet aggregates and thromboxane A2 production.血小板存在分泌缺陷、颗粒储存正常且血栓素A2生成正常时,其(33P)2MeS-ADP结合位点缺乏。有证据表明,ADP增强血小板分泌独立于大血小板聚集体的形成及血栓素A2的生成。
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[Thrombocyte function in vitro in storage over 5 days].
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引用本文的文献

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J Clin Med. 2021 Dec 26;11(1):118. doi: 10.3390/jcm11010118.
2
Impaired mitochondrial activity explains platelet dysfunction in thrombocytopenic cancer patients undergoing chemotherapy.线粒体活性受损解释了正在接受化疗的血小板减少症癌症患者的血小板功能障碍。
Haematologica. 2018 Sep;103(9):1557-1567. doi: 10.3324/haematol.2017.185165. Epub 2018 Jun 7.
3
Membrane transport and disease.膜转运与疾病
Mol Cell Biochem. 1989;91(1-2):3-11. doi: 10.1007/BF00228073.

本文引用的文献

1
Biochemical and metabolic aspects of platelet dysfunction in chronic myeloproliferative disorders.慢性骨髓增殖性疾病中血小板功能障碍的生化和代谢方面
Thromb Haemost. 1982 Apr 30;47(2):84-9.
2
Relationship of megakaryocyte size at diagnosis to chemotherapeutic response in children with acute nonlymphocytic leukemia.急性非淋巴细胞白血病患儿诊断时巨核细胞大小与化疗反应的关系。
Blood. 1983 May;61(5):867-70.
3
Relationship between platelet aggregation, thromboxane synthesis and albumin concentration in nephrotic syndrome.肾病综合征中血小板聚集、血栓素合成与白蛋白浓度之间的关系。
Br J Haematol. 1982 Sep;52(1):69-77. doi: 10.1111/j.1365-2141.1982.tb03862.x.
4
Plasma beta-thromboglobulin values in thrombocytopenic patients with acute leukemia.急性白血病血小板减少患者的血浆β-血小板球蛋白值
Am J Hematol. 1980;8(4):339-45. doi: 10.1002/ajh.2830080402.
5
Severe platelet dysfunction in hairy cell leukemia with improvement after splenectomy.毛细胞白血病中的严重血小板功能障碍,脾切除术后有所改善。
Blood. 1980 Jun;55(6):903-6.
6
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
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Thrombokinetics in acute nonlymphocytic leukemia.急性非淋巴细胞白血病的血栓动力学
J Lab Clin Med. 1973 Dec;82(6):911-23.
8
Qualitative platelet defects with reduced life-span in acute leukaemia.急性白血病中伴有血小板寿命缩短的定性血小板缺陷。
Aust N Z J Med. 1972 Nov;2(4):339-45. doi: 10.1111/j.1445-5994.1972.tb03934.x.
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Platelet function in acute leukemia.急性白血病中的血小板功能
J Lab Clin Med. 1972 Jun;79(6):893-905.
10
Platelet storage pool deficiency and prostaglandin synthesis in chronic granulocytic leukaemia.慢性粒细胞白血病中的血小板储存池缺陷与前列腺素合成
Br J Haematol. 1978 Dec;40(4):597-607. doi: 10.1111/j.1365-2141.1978.tb05836.x.