Polycythemia in the Young

Authors

  • Insiripong S, Yingsitsiri W, Boondumrongsagul J

Keywords:

Polycythemia, The Young, Polycythemia Vera

References

Tefferi A, Thiele J, Vardiman JW. The 2008 World Health Organization classification system for myeloproliferative neoplasms: order out of chaos. Cancer 2009; 115: 3842-7.

Fujita H, Kurosawa S, Nishimura S, Tomiyama J, Hamaki T, Ohwada A. Significance of microcytosis in the clinical course of erythrocytosis. Internet J Geriatr Gerontol 2009; 6: 1-6.

Najean Y, Mugnier P, Dresch C, Rain JD. Polycythaemia vera in young people: an analysis of 58 cases diagnosed before 40 years. Br J Haematol 1987; 67: 285-91.

Passamonti F, Malabarba L, Orlandi E, Baratè C, Canevari A, Brusamolino E, et al. Polycythemia vera in young patients: a study on the long-term risk of thrombosis, myelofibrosis and leukemia. Haematologica 2003; 88: 13-8.

Cario H, McMullin MF, Pahl HL. Clinical and hematological presentation of children and adolescents with polycythemia vera. Ann Hematol 2009; 88: 713-9.

Tefferi A, Thiele J, Orazi A, Kvasnicka HM, Barbui T, Hanson CA, et al. Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel. Blood 2007; 110: 1092-7.

Giona F, Teofili L, Moleti ML, Martini M, Palumbo G, Amendola A, et al. Thrombocythemia and polycythemia in patients younger than 20 years at diagnosis: clinical and biologic features, treatment, and long-term outcome. Blood 2012; 119: 2219-27.

McMullin MF. The classification and diagnosis of erythrocytosis. Int J Lab Hematol. 2008; 30: 447–59.

Watts EJ, Lewis SM. Spurious polycythemia-a study of 35 patients. Scand J Haematol 1983; 31: 241-7.

Johansson PL, Safai-Kutti S, Kutti J. An elevated venous haemoglobin concentration cannot be used as a surrogate marker for absolute erythrocytosis: a study of patients with polycythaemia vera and apparent polycythaemia. Br J Haematol 2005; 129: 701-5.

Williams DM, Kim AH, Rogers O, Spivak JL, Moliterno AR. Phenotypic variations and new mutations in JAK2 V617F-negative polycythemia vera, erythrocytosis, and idiopathic myelofibrosis. Exp Hematol 2007; 35: 1641–6.

Pietra D, Li S, Brisci A, Passamonti F, Rumi E, Theocharides A, et al. Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood 2008; 111: 1686–9.

Spivak JL, Silver RT. The revised World Health Organization diagnostic criteria for polycythemia vera, essential thrombocytosis, and primary myelofibrosis: an alternative proposal. Blood 2008; 112: 231-9.

Landgren O, Goldin LR, Kristinsson SY, Helgadottir EA, Samuelsson J, Björkholm M. Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24,577 first-degree relatives of 11,039 patients with myeloproliferative neoplasms in Sweden. Blood 2008; 112: 2199-204.

Ranjan A, Penninga E, Jelsig AM, Hasselbalch HC, Bjerrum OW. Inheritance of the chronic myeloproliferative neoplasms. A systematic review. Clin Genet 2013; 83: 99-107.

Weinfeld A, Swolin B, Westin J. Acute leukaemia after hydroxyurea therapy in polycythaemia vera and allied disorders: prospective study of efficacy and leukaemogenicity with therapeutic implications. Eur J Haematol 1994; 52: 134-9.

Downloads

Published

01-02-2017

How to Cite

1.
Insiripong S, Yingsitsiri W, Boondumrongsagul J. Polycythemia in the Young. J DMS [Internet]. 2017 Feb. 1 [cited 2024 May 6];42(1):118-22. Available from: https://he02.tci-thaijo.org/index.php/JDMS/article/view/248921

Issue

Section

Original Article