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血小板计数正常和异常人群骨髓巨核细胞倍性分布的评估。

Evaluation of bone marrow megakaryocyte ploidy distributions in persons with normal and abnormal platelet counts.

作者信息

Mazur E M, Lindquist D L, de Alarcon P A, Cohen J L

机构信息

Department of Medicine, Brown University, Providence, RI.

出版信息

J Lab Clin Med. 1988 Feb;111(2):194-202.

PMID:3276801
Abstract

Using bone marrow smears of the type prepared routinely in clinical practice, we determined megakaryocyte ploidy distributions in five normal persons, eight patients with both normal platelet counts and normal bone marrow morphology, and 18 patients with quantitative platelet disorders. To include 2N and 4N megakaryocytes in the ploidy distribution histograms, all megakaryocytes were identified by serial immunologic labelling with rabbit antiserum to human platelet glycoproteins and rhodamine-conjugated goat anti-rabbit igG. Cell nuclei were concurrently Feulgen stained with bis-aminophenyl-oxdiazole, and the nuclear fluorescent signals were quantified photometrically. A modal megakaryocyte ploidy value of 32N was seen in 10 of the 13 persons with normal platelet counts, and geometric mean megakaryocyte ploidy values averaged 24.9N +/- 7.0N (arithmetic mean +/- SD). In these normal control individuals, 2N and 4N megakaryocytes accounted for 11.1% of all megakaryocytes, and 2.6% of the megakaryocytes were 128N. Shifts to a higher mean ploidy were observed in five of seven patients with idiopathic thrombocytopenic purpura, resulting from increased percentages of 64N and 128N megakaryocytes at the expense of 4N, 8N, and 16N cells. Shifts to lower ploidy were demonstrated in two patients with acute myelogenous leukemia and one patient each with thrombotic thrombocytopenic purpura and isoimmune thrombocytopenia. Four of five patients with essential thrombocythemia had strikingly abnormal megakaryocyte ploidy histograms characterized by the presence of unusually high ploidy 256N and 512N megakaryocytes. These 256N and 512N cells were virtually unique to the patients with essential thrombocythemia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们使用临床实践中常规制备的骨髓涂片,测定了5名正常人、8名血小板计数和骨髓形态均正常的患者以及18名血小板数量异常患者的巨核细胞倍性分布。为了在倍性分布直方图中纳入2N和4N巨核细胞,所有巨核细胞均通过用兔抗人血小板糖蛋白抗血清和罗丹明偶联的山羊抗兔IgG进行系列免疫标记来识别。细胞核同时用双氨基苯基恶二唑进行Feulgen染色,并通过光度法对核荧光信号进行定量。在13名血小板计数正常的人中,有10人观察到巨核细胞倍性的众数为32N,巨核细胞倍性的几何平均值平均为24.9N±7.0N(算术平均值±标准差)。在这些正常对照个体中,2N和4N巨核细胞占所有巨核细胞的11.1%,2.6%的巨核细胞为128N。在7名特发性血小板减少性紫癜患者中的5名中观察到平均倍性向更高值转变,这是由于64N和128N巨核细胞百分比增加,以4N、8N和16N细胞为代价。在2名急性髓性白血病患者以及各1名血栓性血小板减少性紫癜和同种免疫性血小板减少症患者中观察到倍性向更低值转变。5名原发性血小板增多症患者中有4名的巨核细胞倍性直方图异常显著,其特征是存在异常高倍性的256N和512N巨核细胞。这些256N和512N细胞实际上是原发性血小板增多症患者所特有的。(摘要截短于250字)

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