Mutation screening for JAK2V617F: when to order the test and how to interpret the results.

Abstract:

:With the application of adequately sensitive tests, it is now becoming evident that more than 90% of patients with conventionally-defined polycythemia vera (PV) carry the somatic JAK2V617F mutation in their granulocytes. However, the specific mutation is also found in other classic and atypical myeloproliferative disorders (MPD), albeit at a lesser frequency. In contrast, JAK2V617F has not been reported in patients with either reactive myeloproliferation or lymphoid disorders. Therefore, mutation screening for JAK2V617F can be considered as a myeloid-specific clonality assay and it is diagnostically most useful in the evaluation of "polycythemia".

journal_name

Leuk Res

journal_title

Leukemia research

authors

Tefferi A,Pardanani A

doi

10.1016/j.leukres.2006.01.004

keywords:

subject

Has Abstract

pub_date

2006-06-01 00:00:00

pages

739-44

issue

6

eissn

0145-2126

issn

1873-5835

pii

S0145-2126(06)00023-3

journal_volume

30

pub_type

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