论文部分内容阅读
1328 靛玉红治疗原发性血小板增多症一例报告翁维权等中华血液学杂志2(1):64,1981一例46岁男性患者,2年来易有齿龈出血,体征无异常,查血红、白细胞无异常,血小板110万、血块收缩不良,血小板对 ADP 凝聚时间39秒,(正常20秒)。骨髓增生明显活跃,红系、粒系无异常,巨核细胞全片86个,过渡型45%、裸核型20%,成熟型巨核细胞胞本巨大,形态不规则,有分叶过多现象,血小板成堆出现,可见巨大血小
1328 indirubin treatment of primary thrombocytopenia A case report Weng Weigang et al Chinese Journal of Hematology 2 (1): 64,1981 A 46-year-old male patient, 2 years prone to bleeding gums, no abnormal signs, check the red, white blood cells Abnormal, 1.1 million platelets, clot maladjustment, platelet aggregation of ADP 39 seconds, (normal 20 seconds). Myeloid hyperplasia was obviously active. There was no abnormal erythroid and granulocytic lineage. There were 86 megakaryocytes, 45% transitional type and 20% naked nucleus. The megakaryocyte of mature type was huge, with irregular shape and excessive lobulation. Platelets pile up, showing huge blood