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原发性血小板增多症是一种慢性骨髓增殖性疾患,以巨核细胞增生伴持续性血小板增多为其特征。主要发生在中年人,在儿童则罕见。作者报道一家族连续三代女3、男2人发生本症。
Primary thrombocythemia is a chronic myeloproliferative disorder characterized by megakaryocyte hyperplasia with persistent thrombocytopenia. Mainly occurs in middle-aged people, is rare in children. The authors report a family of three consecutive generations of women 3, 2 men and 2 this disease.