Tumour genesis syndrome: severe hypophosphatemia and hypokalemia may be ominous presenting findings in childhood acute myeloid leukaemia-Reference-Cited by-同舟云学术

Tumour genesis syndrome: severe hypophosphatemia and hypokalemia may be ominous presenting findings in childhood acute myeloid leukaemia

Published:2017-05-04 Issue:8 Volume:176 Page:1137-1141
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Chan Winnie KY,Chang Kai On,Lau Wing Hung

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/article/10.1007/s00431-017-2899-7/fulltext.html

Reference15 articles.

1. Brautbar N, Leibovici H, Massry SG (1983) On the mechanism of hypophosphatemia during acute hyperventilation: evidence for increased muscle glycolysis. Miner Electrolyte Metab 9:45–50

2. Dalal BI, Brigden ML (2009) Factitious biochemical measurements resulting from hematologic conditions. Am J Clin Pathol 131:195–204

3. Filippatos TD, Milionis HK, Elisaf MS (2005) Alternations in electrolyte equilibrium in patients with acute leukemia. Eur J Haematol 75:449–460

4. Liamis G, Elisaf M (2000) Hypokalemia, hypophosphatemia and hypouricemia due to proximal renal tubular dysfunction in acute myeloid leukemia. Eur J Haematol 64:277–278

5. Majhail NS, Lichtin AE (2004) Acute leukemia with a very high leukocyte count: confronting a medical emergency. Cleve Clin J Med 71(8):633–637

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4. Erratum to: Tumour genesis syndrome: severe hypophosphatemia and hypokalemia may be ominous presenting findings in childhood acute myeloid leukaemia;European Journal of Pediatrics;2017-07-03