难治性慢性免疫性血小板减少症的巨核细胞生成。

N Suvajdzić, Z Rolović, I Elezović, M Colović
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引用次数: 7

摘要

对14例严重难治性慢性免疫性血小板减少症(rchr ITP)患者的巨核细胞增生(Mk-poiesis)程度和临床结果进行了评估。14名患者中有3人因出血死亡。出血次数和治疗方式数量均为预后生存的敏感参数(p < 0.05)。32例皮质类固醇反应性chr ITP患者(chr ITPPR), 15例未治疗患者(chr ITP(NT))和14名健康志愿者(C)作为对照。两组患者血小板计数比较,差异有统计学意义(p < 0.05)。rchr ITP患者骨髓中每mm3的巨核细胞和前巨核母细胞数量显著低于chr ITP(PR)组和chr ITP(NT)组(p < 0.05),提示rITP chr患者mk生成不足。从这里提供的数据可以看出,rchr ITP的mk - poesis不足。
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Megakaryocytopoiesis in refractory chronic immune thrombocytopenia.

The extent of megakaryocytopoiesis (Mk-poiesis) and clinical outcome are evaluated in 14 patients with severe refractory chronic immune thrombocytopenia (rchr ITP). Three out of 14 patients died due to hemorrhage. The number of bleeding episodes and the number of treatment modalities proved to be both sensitive prognostic survival parameters (p < 0.05). Thirty two corticosteroid responsive chr ITP patients (chr ITPPR), 15 not treated patients (chr ITP(NT)) and 14 healthy volunteers (C) served as a control. There was a significant difference in the platelet count between the study groups (p < 0.05). The number of megakaryocytes and promegakaryoblasts per mm3 of bone marrow were significantly lower in rchr ITP patients (p < 0.05) than in chr ITP(PR) and in chr ITP(NT) group, thus implying an inadequate Mk-poiesis in rITP chr patients. From the data presented here it may be suggested that the inadequate Mk-poiesis is operating in rchr ITP.

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