Prodromal myeloproliferative neoplasms: The 2008 WHO classification

被引:61
作者
Kvasnicka, Hans Michael [1 ]
Thiele, Juergen [1 ]
机构
[1] Univ Cologne, Inst Pathol, D-50924 Cologne, Germany
关键词
CHRONIC IDIOPATHIC MYELOFIBROSIS; JAK2 V617F MUTATION; BONE-MARROW FEATURES; ORGANIZATION DIAGNOSTIC-CRITERIA; AGNOGENIC MYELOID METAPLASIA; INTERNATIONAL WORKING GROUP; ERYTHROID COLONY FORMATION; ESSENTIAL THROMBOCYTHEMIA MYELOFIBROSIS; TYROSINE KINASE MUTATION; PORTAL-VEIN THROMBOSIS;
D O I
10.1002/ajh.21543
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The concept of prodromal chronic myeloproliferative neoplasms has been endorsed by the WHO classification implicating a stepwise evolution of disease. Histology of the bone marrow (BM) and borderline to mildly expressed clinical features play a pivotal role for diagnosing prefibrotic-early primary myelofibrosis. By lowering the platelet count for essential thrombocythemia and regarding BM morphology, early manifestations are tackled. Pre-polycythemic stages of polycythemia vera with a low hemoglobin level at onset are diagnosed by positive JAK2V617F mutation status, a low erythropoietin value, and characteristic BM features. The revised WHO classification incorporates hematological, morphological, and moleculargenetic parameters to generate a consensus-based working diagnosis. Am. J. Hematol. 85:62-69, 2010. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:62 / 69
页数:8
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