Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms.

作者: A Tefferi , J W Vardiman

DOI: 10.1038/SJ.LEU.2404955

关键词: Chronic neutrophilic leukemiaMyeloproliferative DisordersOncologyImmunologyInternal medicineChronic eosinophilic leukemiaPolycythemia veraMyelofibrosisHypereosinophilic syndromeMedicineEssential thrombocythemiaMyelogenous

摘要: The 2001 World Health Organization (WHO) treatise on the classification of hematopoietic tumors lists chronic myeloproliferative diseases (CMPDs) as a subdivision myeloid neoplasms that includes four classic disorders (MPDs)-chronic myelogenous leukemia, polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (PMF)-as well neutrophilic leukemia (CNL), eosinophilic leukemia/hypereosinophilic syndrome (CEL/HES) 'CMPD, unclassifiable'. In upcoming 4th edition WHO document, due out in 2008, term 'CMPDs' is replaced by 'myeloproliferative (MPNs)', MPN category now mast cell disease (MCD), addition to other subcategories mentioned above. At same time, however, with molecularly characterized clonal eosinophilia, previously classified under CEL/HES, are removed from section assembled into new their own. diagnostic criteria for both BCR-ABL-negative MPDs (that PV, ET PMF) CEL/HES have also been revised, 2008 edition, incorporating information molecular pathogenesis. current review highlights these changes provides algorithms tailored routine clinical practice.

参考文章(111)
Nathaniel I. Berlin, Diagnosis and classification of the polycythemias Seminars in Hematology. ,vol. 12, pp. 339- 351 ,(1975) , 10.5555/URI:PII:0037196375900098
Animesh Pardanani, Ayalew Tefferi, Systemic mastocytosis: current concepts and treatment advances. Current hematology reports. ,vol. 3, pp. 197- 202 ,(2004)
Hsiao-Wen Chang, Kah-Hoo Leong, Dow-Rhoon Koh, Szu-Hee Lee, Clonality of Isolated Eosinophils in the Hypereosinophilic Syndrome Blood. ,vol. 93, pp. 1651- 1657 ,(1999) , 10.1182/BLOOD.V93.5.1651
G Morgan, JM Goldman, F Rassool, Philippe Martiat, J Gow, Norbert Ifrah, F Giles, Molecular analysis of Philadelphia positive essential thrombocythemia. Leukemia. ,vol. 3, pp. 563- 565 ,(1989)
Shireen Sirhan, Virgil F. Fairbanks, Ayalew Tefferi, Red cell mass and plasma volume measurements in polycythemia: Cancer. ,vol. 104, pp. 213- 215 ,(2005) , 10.1002/CNCR.21105
PJ Fialkow, GB Faguet, RJ Jacobson, K Vaidya, S Murphy, Evidence that essential thrombocythemia is a clonal disorder with origin in a multipotent stem cell Blood. ,vol. 58, pp. 916- 919 ,(1981) , 10.1182/BLOOD.V58.5.916.916
Jamie Robyn, Steven Lemery, J. Philip McCoy, Joseph Kubofcik, Yae-Jean Kim, Svetlana Pack, Thomas B. Nutman, Cynthia Dunbar, Amy D. Klion, Multilineage involvement of the fusion gene in patients with FIP1L1/PDGFRA-positive hypereosinophilic syndrome British Journal of Haematology. ,vol. 132, pp. 286- 292 ,(2006) , 10.1111/J.1365-2141.2005.05863.X
Elias Campo, N Lee Harris, Elaine S Jaffe, Stefano A Pileri, Harald Stein, Jurgen Thiele, James W Vardiman, None, WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues ,(2017)