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原发性骨髓纤维化(IMF)是一种少见的克隆增殖性疾病,其临床特征存在很大的异质性。我们回顾性分析了127例IMF患者的临床资料,报道如下。1临床资料127例系1971-02～2001-09中国协和医科大学血液学研究所血液病医院门诊及住院IMF患者,符合国内血液病诊断及疗效标准[1]。男69例,女
Primary myelofibrosis (IMF) is a rare clonal proliferative disease with a large heterogeneity of clinical features. We retrospectively analyzed the clinical data of 127 cases of IMF patients, reported as follows. 1 clinical data 127 cases 1971-02 ~ 2001-09 Peking Union Medical College Hematology Institute of hematology hospital outpatient and inpatient IMF patients, in line with the domestic blood disease diagnosis and efficacy standards [1]. 69 males and females