Literature DB >> 8949586

Investigation of patients with polycythaemia.

T C Pearson1, M Messinezy.   

Abstract

Polycythaemia may complicate or be the presenting feature of a wide variety of different pathologies. Early diagnosis and treatment of primary polycythaemia will significantly reduce the morbidity and mortality associated with this condition. Patients with a raised packed cell volume are divided into those with a raised red cell mass (absolute polycythaemia), and those with a red cell mass within their normal range (apparent polycythaemia). A standard investigative approach of an absolute polycythaemia enables patients with primary and secondary polycythaemia to be identified, leaving a group termed idiopathic erythrocytosis. There are a number of physiological situations and pathological events associated with idiopathic erythrocytosis and apparent polycythaemia. Careful follow-up of both groups of these patients is essential to identify possible causative mechanisms.

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Year:  1996        PMID: 8949586      PMCID: PMC2398572          DOI: 10.1136/pgmj.72.851.519

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN: 0032-5473            Impact factor:   2.401


  19 in total

1.  Complications and causes of death in polycythaemia vera.

Authors:  E CHIEVITZ; T THIEDE
Journal:  Acta Med Scand       Date:  1962-11

2.  A retrospective study of apparent and relative polycythaemia: associated factors and early outcome.

Authors:  M Messinezy; T C Pearson
Journal:  Clin Lab Haematol       Date:  1990

3.  The arterial complications of polycythaemia vera.

Authors:  A P Barabas; D N Offen; E A Meinhard
Journal:  Br J Surg       Date:  1973-03       Impact factor: 6.939

4.  Interpretation of measured red cell mass and plasma volume in adults: Expert Panel on Radionuclides of the International Council for Standardization in Haematology.

Authors:  T C Pearson; D L Guthrie; J Simpson; S Chinn; G Barosi; A Ferrant; S M Lewis; Y Najean
Journal:  Br J Haematol       Date:  1995-04       Impact factor: 6.998

5.  Erythrocytosis associated with diffuse parenchymal lesions of the kidney.

Authors:  E C Hoppin; T Depner; H Yamuchi; J Hopper
Journal:  Br J Haematol       Date:  1976-04       Impact factor: 6.998

6.  Low serum erythropoietin--a strong diagnostic criterion of primary polycythaemia even at normal haemoglobin levels.

Authors:  M Messinezy; N B Westwood; S P Woodcock; R M Strong; T C Pearson
Journal:  Clin Lab Haematol       Date:  1995-09

7.  Tissue specificity of X-chromosome inactivation patterns.

Authors:  R E Gale; H Wheadon; P Boulos; D C Linch
Journal:  Blood       Date:  1994-05-15       Impact factor: 22.113

Review 8.  Apparent polycythaemia.

Authors:  T C Pearson
Journal:  Blood Rev       Date:  1991-12       Impact factor: 8.250

9.  Idiopathic erythrocytosis--additional new study techniques suggest a heterogenous group.

Authors:  M Messinezy; B Sawyer; N B Westwood; T C Pearson
Journal:  Eur J Haematol       Date:  1994-09       Impact factor: 2.997

10.  Primary polycythaemia: positive diagnosis using the differential response of primitive and mature erythroid progenitors to erythropoietin, interleukin 3 and alpha-interferon.

Authors:  J M Dudley; N Westwood; S Leonard; S Eridani; T C Pearson
Journal:  Br J Haematol       Date:  1990-06       Impact factor: 6.998

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