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2008 WHO指南:真性红细胞增多症、原发性血小板增多症及原发性骨髓纤维化的诊断标准

发布日期:2008-01-01

制定者:世界卫生组织(WHO)

来源:WHO官网.

概述

Several international working groups cooperated to propose new diagnostic guidelines for polycythemia vera (PV), essential thrombocythemia (ET), and primary myelofi brosis (PMF) to the steering committee of the World Health Organization. Because JAK2 mutation status presents a decisive diagnostic test in PV, this feature was introduced as a major criterion. Minor criteria, such as characteristic bone marrow morphology, low erythropoietin level, and erythroid colony formation, were kept as supporting parameters. In PMF, major diagnostic criteria were established by histologic features independent of the presence of relevant fi brosis or myelofi brosis with myeloid metaplasia. JAK2 mutation status was restricted to positive fi ndings to exclude reactive myelofi brosis. A decrease in the platelet level was proposed for ET, because vascular complications may occur at lower platelet counts. As with PMF, morphology plays a distinctive role in diagnosis, particularly for its differentiation from early-stage PV or prodromal PMF associated with thrombocytosis.