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Table of Contents
Vol. 74, No. 2, 2007
Issue release date: June 2007
Section title: Review
Pathobiology 2007;74:72–80

Histological and Molecular Classification of Chronic Myeloproliferative Disorders in the Age of JAK2: Persistence of Old Questions despite New Answers

Hussein K. · Bock O. · Kreipe H.
Institute of Pathology, Hannover Medical School, Hannover, Germany
email Corresponding Author

Prof. Hans Kreipe

Institute of Pathology, Medizinische Hochschule Hannover

Carl-Neuberg-Strasse 1

DE–30625 Hannover (Germany)

Tel. +49 511 532 4501, Fax +49 511 532 5799, E-Mail Kreipe.Hans@MH-Hannover.de

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The discovery of the Janus kinase 2 gain-of-function V617F mutation (JAK2V617F) provided a major breakthrough in the understanding of Philadelphia chromosome-negative chronic myeloproliferative disorders (Ph CMPD). Among haematologic neoplasm the mutation appears to be almost specific for Ph CMPD but the different entities comprising polycythaemia vera (PV), essential thrombocythaemia and chronic idiopathic myelofibrosis (CIMF) are not discriminated by the mutation. It is unclear how the diversity with heterogeneous clinical and pathoanatomical presentations comes about. It has been suggested that differences in JAK2V617F gene dosage or different degrees to which the haematologic lineages are affected by the mutation could explain the heterogeneity of morphology and prognosis. Indeed the mutation mediates a PV-like phenotype but with regard to myelofibrosis JAK2V617F does not appear to be a causative factor. Megakaryocytes are homozygous in the majority of fibrotic CIMF and PV, whereas JAK2V617F heterozygosity is predominantly encountered in prefibrotic CIMF and essential thrombocythaemia but transition from hetero- to homozygosity with onset of fibrosis is rare. In conclusion, JAK2V617F provides a valuable adjunct to the diagnosis of Ph CMPD, in particular with regard to discrimination from reactive proliferations, but the challenge of correct subtyping and hence prognostication persists for clinicians and bone marrow pathologists.

© 2007 S. Karger AG, Basel

Article / Publication Details

First-Page Preview
Abstract of Review

Published online: June 25, 2007
Issue release date: June 2007

Number of Print Pages: 9
Number of Figures: 0
Number of Tables: 1

ISSN: 1015-2008 (Print)
eISSN: 1423-0291 (Online)

For additional information: http://www.karger.com/PAT

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