[造血发育不良的预后(作者译)]。

C Dresch, A Faille, A Glogowski, Y Najean
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引用次数: 0

摘要

用铁动力学研究了90例造血发育不良(白血病前期)患者贫血的机制,其中23例进行了骨髓放射自显影,18例在半固体培养基中进行了骨髓培养。一半的病例是由急性髓细胞白血病转化(LAM)引起的,一半的病例是由全血细胞减少症(感染、出血)或血色素沉着症引起的并发症引起的。三个数据给出了短期或长期的预后因素:骨髓发育不全,无严重骨髓发育不全患者(肝脏和骶骨的59Fe固定比大于2)在检查后存活超过2年。成髓细胞和早幼髓细胞的标记指数低,研究结束后生活不到一年的患者的平均LI为0.20,生活超过两年的患者的平均LI为0.35。大聚集型骨髓培养,研究后没有患者骨髓生长有大聚集,没有菌落存活超过8个月。这三个数据在hemopoïetic发育不良患者的常规调查中似乎是必不可少的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Prognosis of hematopoietic dysplasia (author's transl)].

90 patients with hemopoietic dysplasia (preleukemia) have been studied with iron kinetics for the mechanism of the anaemia, 23 patients had a bone marrow autoradiography and 18 a bone marrow culture in semi-solid medium. The death was caused in half the cases by acute myeloblastic leukaemia transformation (LAM) and in half the cases by complications of pancytopenia (infection, haemorrhage) or hemochromatosis. Three data give prognostic factors at short or long term: the bone marrow hypoplasia, no patient with major bone marrow hypoplasia (ratio of 59Fe fixation in liver and sacrum of more than 2) lived more than 2 years after the examination. The low labeling index of myeloblasts and promyelocytes, the mean LI is 0.20 patients having lived less than one year after the study and 0.35 for those who lived more than two years. The bone marrow culture of the macroclusters type, no patient whose bone marrow grew with macroclusters and no colonies survived more than 8 months after the study. These three data seem to be essential in the regular survey of the patients with hemopoïetic dysplasia.

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