Turtureanu-Hanganu E, Ungureanu E
Rev Med Chir Soc Med Nat Iasi. 1989 Jul-Sep;93(3):481-3.
The authors presents her experience in polycythaemia rubra vera. A number of 20 cases have been studied, with a peak of polycythaemic values of 20.6/dl for the Hb, a Ht of 80%, an WBC count of 28,000/cmm and a platelet count of 1,400,000/cmm. The following peculiarities of the cases should be underlined: 1. the personal and hereditary collateral antecedents which reveal a significant pathological background; 2. the very slow evolutive potential of the malignant erythroid clone, which permitted a quasi-normal way of life for many years; 3. a careful therapy, differentiated with respect to the evolutive stage of disease, which resulted in a long survival (over 17 years).
作者介绍了她在真性红细胞增多症方面的经验。已对20例病例进行了研究，血红蛋白的红细胞增多值峰值为20.6/dl，血细胞比容为80%，白细胞计数为28,000/cmm，血小板计数为1,400,000/cmm。应强调这些病例的以下特点：1. 个人及遗传旁系病史揭示了重要的病理背景；2. 恶性红系克隆的演变潜力非常缓慢，这使得许多患者多年来能维持近乎正常的生活方式；3. 根据疾病的演变阶段进行的精心治疗，使患者获得了较长的生存期（超过17年）。
