Familial thrombocytosis in infancy presenting with a leukaemoid reaction

Acta Paediatrica, International Journal of Paediatrics

Volumn 85, Issue 9, 1996, Pages 1132-1134

  Van Dijken, P J ^a,b   Woldendorp, K H ^a   Van Wouwe, J P ^c  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b The General Directorate of Armed Forces Health Services   (Saudi Arabia)

^c Drechtsteden Ziekenhuis   (Netherlands)

Author keywords

Chronic myelocytic leukaemia; Essential thrombocytosis; Familial thrombocytosis

Indexed keywords

ARTICLE; BONE MARROW BIOPSY; CASE REPORT; CHRONIC MYELOID LEUKEMIA; CONTROLLED STUDY; FAILURE TO THRIVE; FAMILIAL DISEASE; FOLLOW UP; HEPATOSPLENOMEGALY; HUMAN; HUMAN CELL; INFANT; LEUKEMOID REACTION; MALE; MEGAKARYOPOIESIS; PRIORITY JOURNAL; THROMBOCYTOSIS;

EID: 0029743453     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1651-2227.1996.tb14234.x     Document Type: Article

References (20)

1. Linch DC, Hutton R, Cowan D, Moore AR, Richards JDM, Wilkinson LS. Primary thrombocythemia in childhood. Scand J Haematol 1982;28:72-6
2. Pearson TC. Primary thrombocythaemia: diagnosis and treatment. Br J Haematol 1991;78:145-8
3. Randi ML, Fabris F, Visentin I, Girolami A. Low incidence of familial occurrence of thrombocythaemia and or thrombocytosis. Folia Haematol (Leipz) 1988;115:695-9
4. Janssen JWG, Anger HG, Drexler HG, Bartram CR, Heimpel H. Essential thrombocythemia in two sisters originating from different stem cell levels. Blood 1990;75:1633-6
5. Perez-Encinas M, Bello JL, Perez-Crespo, De Miguel R, Tome S. Familial myeloproliferative syndrome. Am J Hematol 1994;46: 225-9
6. Beretta Anguissola A, Prato V. Trombocitosi ereditaria, prima osservazione. Minerva Med 1961;52:4545-8
7. Pickers M, Speck B. Thrombocythaemia. Familial occurrence and transition into blastic crisis. Acta Haematol 1974;51:257-65
8. Slee PHTJ, van Everdingen JJE, Geraedts JPM, te Velde J, den Ottolander GJ. Familial myeloproliferative disease. Haematological and cytogenetic studies. Acta Med Scand 1981;210:321-7
9. Eyster MF, Saletan SL, Rabellino EM, Karanas A, McDonald TP, Locke LA, et al. Familial essential thrombocythemia. Am J Med 1986;80:497-502
10. Fernandez-Robles E, Vermylen C, Martiat P, Ninane J, Cornu G. Familial essential thrombocythemia. Pediatr Hematol Oncol 1990;7:373-6
11. Williams EC, Shahidi NT. Benign familial thrombocytosis. Am J Hematol 1991;37:124-5
12. Schlemper RJ, van der Maas AP, Eykenboom JC. Familial essential thrombocythemia: clinical characteristics of eleven cases. Ann Hematol 1994;68:153-8
13. Hehlmann R, Jahn M, Baumann B, Koepcke W. Essential thrombocythemia: clinical characteristics and course of 61 patients. Cancer 1988;61:2487
14. Freedman MH, Estrov Z, Chan HSL. Juvenile chronic myelogenous leukemia. Am J Pediatr Hematol Oncol 1988;10:261-7
15. McNiel JR. The possible teratogenic effect of salicylates on the developing fetus. Brief summaries of eight suggestive cases. Clin Pediatr 1973;12:347-50
16. Belucci S, Gautier M, Tobelern G, Flandrin G, Charpa K, Berger R, Doiron M. Essential thrombocythemia: clinical evolution and histological data. Cancer 1986;58:2440-6
17. Dodsworth H. Primary thrombocythaemia in monozygotic twins. Br Med J 1980;280:1506
18. Dedichen J, Refvem O, Ytrehus K. Essential thrombocythaemia. Nordisk Medicin 1959;62:1265-70
19. Schultz Beardsley D. Platelet abnormalities in infancy and childhood. In: Nathan DG, Oski FA, editors. Hematology of infancy and childhood. 4th ed. Philadelphia: WB Saunders, 1993:1561-604
20. Bokarewa MI, Bremme K, Falk G, Sten-Linder M, Egberg N, Blomback M. Studies on phospholipid antibodies. APC-resistance and associated mutation in the coagulation factor V gene. Thromb Res 1995;78:193-200