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Masked polycythemia vera diagnosed according to WHO and BCSH classification

Authors :
Tiziano Barbui
Marco Ruggeri
Ayalew Tefferi
Heinz Gisslinger
Alessandra Carobbio
Elisa Rumi
Bettina Gisslinger
Alessandro Rambaldi
Maria Luigia Randi
Guido Finazzi
Alessandro M. Vannucchi
Leonhard Müllauer
Jürgen Thiele
Source :
American Journal of Hematology. 89:199-202
Publication Year :
2014
Publisher :
Wiley, 2014.

Abstract

Polycythemia vera (PV) is currently diagnosed by the World Health Organization (WHO) criteria regarding hemoglobin (HB) levels and JAK2V617F and related mutations or by the British Committee for Standards in Haematology (BCSH) guidelines predominantly based on hematocrit (HCT) values (>52% in men and >48% in women) in JAK2 mutated patients. We examined clinical features at diagnosis and outcome in 397 mutated PV patients showing a bone marrow (BM) morphology conforming with the WHO descriptions but including also cases with a HB level 65 years and white blood cell count >15 × 10(9) /L. Without these risk factors mPV patients had the same survival as overt PV suggesting that a fraction of patients with HB lower than that required for WHO diagnosis should still be considered as overt PV. This study has established the existence of mPV by two different classification systems based on either HB or HCT threshold values.

Details

ISSN :
03618609
Volume :
89
Database :
OpenAIRE
Journal :
American Journal of Hematology
Accession number :
edsair.doi...........63704cde6ee52a375429c910d4047c72
Full Text :
https://doi.org/10.1002/ajh.23617