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关于“白血病前期”病程及预后标准的前瞻性研究(作者译)

[A prospective study on course and prognostic criteria in "preleukemia" (author's transl)].

作者信息

Heimpel H, Drings P, Mitrou P, Queisser W

出版信息

Klin Wochenschr. 1979 Jan 1;57(1):21-9. doi: 10.1007/BF01476978.

Abstract

The natural course of disease was followed in 33 patients with so-called preleukemia by a prospective multicentric protocol. Patients with the following criteria were included: Anaemia with granulocytopenia and/or thrombocytopenia, normal or increased cellularity of the bone marrow and exclusion of a known diagnosis of underlying disease. Follow up after assumption of "preleukemia" was 3 years or more. Median survival was 26 months after diagnosis of preleukemia and 36 months after the first unequivocal symptoms of the blood dyscrasia. 40% of the patients changed to the picture of leukemia within 2 years. The most important parameters suggesting subsequent transition to overt leukemia where chromosomal abberations and an increased blast count of the bone marrow.

摘要

通过一项前瞻性多中心方案,对33例所谓的白血病前期患者的疾病自然病程进行了跟踪研究。纳入符合以下标准的患者:伴有粒细胞减少和/或血小板减少的贫血、骨髓细胞数量正常或增加,且排除已知的潜在疾病诊断。确诊“白血病前期”后的随访时间为3年或更长时间。白血病前期诊断后的中位生存期为26个月,血液恶液质首次明确症状出现后的中位生存期为36个月。40%的患者在2年内转变为白血病状态。提示随后转变为明显白血病的最重要参数是染色体畸变和骨髓原始细胞计数增加。

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