The classification and diagnosis of erythrocytosis

被引:75
作者
McMullin, M. F. [1 ]
机构
[1] Queens Univ Belfast, Dept Haematol, Belfast BT9 7AB, Antrim, North Ireland
关键词
Polycythaemia vera; erythrocytosis; erythropoietin;
D O I
10.1111/j.1751-553X.2008.01102.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
An absolute erythrocytosis is present when the red cell mass is raised and the haematocrit is elevated above prescribed limits. Causes of an absolute erythrocytosis can be primary where there is an intrinsic problem in the bone marrow and secondary where there an event outside the bone marrow driving erythropoiesis. This can further be divided into congenital and acquired causes. There remain an unexplained group idiopathic erythrocytosis. Investigation commencing with thorough history taking and examination and then investigation depending on initial features is required. Clear simple criteria for polycythaemia vera are now defined. Those who do not fulfil these criteria require further investigation depending on the clinical scenario and initial results. The erythropoietin level provides some guidance as to the direction in which to proceed and the order and extent of investigation necessary in an individual patient. It should thus be possible to make an accurate diagnosis in the majority of patients.
引用
收藏
页码:447 / 459
页数:13
相关论文
共 76 条
[1]   POLYCYTHEMIA-VERA - STEM-CELL AND PROBABLE CLONAL ORIGIN OF DISEASE [J].
ADAMSON, JW ;
FIALKOW, PJ ;
MURPHY, S ;
PRCHAL, JF ;
STEINMANN, L .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (17) :913-916
[2]   Endemic polycythemia in Russia: Mutation in the VHL gene [J].
Ang, SO ;
Chen, H ;
Gordeuk, VR ;
Sergueeva, AI ;
Polyakova, LA ;
Miasnikova, GY ;
Kralovics, R ;
Stockton, DW ;
Prchal, JT .
BLOOD CELLS MOLECULES AND DISEASES, 2002, 28 (01) :57-62
[3]   A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis [J].
Arcasoy, MO ;
Karayal, AF ;
Segal, HM ;
Sinning, JG ;
Forget, BG .
BLOOD, 2002, 99 (08) :3066-3069
[4]   Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene [J].
Arcasoy, MO ;
Degar, BA ;
Harris, KW ;
Forget, BG .
BLOOD, 1997, 89 (12) :4628-4635
[5]   Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders [J].
Baxter, EJ ;
Scott, LM ;
Campbell, PJ ;
East, C ;
Fourouclas, N ;
Swanton, S ;
Vassiliou, GS ;
Bench, AJ ;
Boyd, EM ;
Curtin, N ;
Scott, MA ;
Erber, WN ;
Green, AR .
LANCET, 2005, 365 (9464) :1054-1061
[6]  
Berk PD., 1995, Polycythemia Vera and the Myeloproliferative Disorders, P166
[7]   Erythrocytosis after renal transplantation represents an abnormality of insulin-like growth factor-I and its binding proteins [J].
Brox, AG ;
Mangel, J ;
Hanley, JA ;
St Louis, G ;
Mongrain, S ;
Gagnon, RF .
TRANSPLANTATION, 1998, 66 (08) :1053-1058
[8]  
BRUNEVAL P, 1993, BLOOD, V81, P1593
[9]   CIGARETTE-SMOKING AND SECONDARY POLYCYTHEMIA IN HYPOXIC COR-PULMONALE [J].
CALVERLEY, PMA ;
LEGGETT, RJ ;
MCELDERRY, L ;
FLENLEY, DC .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1982, 125 (05) :507-510
[10]  
Campbell PJ, 2006, METH MOLEC MED, V125, P253