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

被引:5
作者
Chan, Winnie K. Y. [1 ]
Chang, Kai On [1 ]
Lau, Wing Hung [1 ]
机构
[1] Queen Elizabeth Hosp, Dept Paediat, Hong Kong, Hong Kong, Peoples R China
关键词
Tumour genesis syndrome; Hypophosphatemia; Hypokalemia; Acute renal failure; Electrolyte disorder; RENAL TUBULAR DYSFUNCTION; MARKED HYPOPHOSPHATEMIA; PATIENT; ELECTROLYTE;
D O I
10.1007/s00431-017-2899-7
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
We report a 16-year-old girl who was diagnosed with acute leukaemia and a marked leucocytosis > 200 x 10(9)/L. She presented with marked hypophosphatemia, hypokalemia, acute renal failure and acute respiratory failure. These electrolytes disturbances may indicate rapid tumour genesis. These ominous findings required urgent treatment to halt the crises of rapid leukemic cell proliferation. Conclusion: Mark hypophosphatemia and hypokalemia may be presenting electrolyte abnormalities in a patient with acute leukaemia, and these may be indicators of aggressive tumour genesis.
引用
收藏
页码:1137 / 1141
页数:5
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