2020, Number 3
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Rev Hematol Mex 2020; 21 (3)
Spontaneous tumor lysis syndrome
Gutiérrez-Aguirre CH, Castro-Gutiérrez PM, Contreras-Ruiz F, Colunga-Pedraza P, Jaime-Pérez JC, Gómez-Almaguer D
Language: Spanish
References: 14
Page: 172-178
PDF size: 270.09 Kb.
ABSTRACT
Background: Tumor lysis syndrome is the most frequent oncological emergency
resulting from severe electrolytic and metabolic imbalance due to intracellular emptying
of ions and metabolites by the destruction of neoplastic cells. The main laboratory
alterations are hyperuricemia, hypercalcemia, hyperphosphatemia, hyperkalemia and
hypocalcemia. There are two types of presentations, induced tumor lysis syndrome,
in which its etiology is mainly linked to treatment, including chemotherapy and radiotherapy,
steroids, biological immunomodulators and monoclonal antibodies, and
spontaneous tumor lysis syndrome, observed in a third of cases, in which the pathophysiology
remains unknown, but it is presented in the absence of treatment and is
associated with a higher mortality. Within hematological malignancies, tumor lysis
syndrome is more frequently observed in acute leukemias.
Clinical case: A 31-year-old male patient in the blast phase of chronic granulocytic
leukemia presenting with a spontaneous tumor lysis syndrome.
Conclusions: Spontaneous tumor lysis syndrome is a potentially mortal complication
observed in different neoplasms, more frequently in hematologic ones. It is
necessary to remember its characteristics and suspect it to initiate the treatment as
soon as possible.
REFERENCES
Ñamendys S, Arredondo J, Plata E, Guevara H, Garcia F, Rivero E, et al. Tumor lysis syndrome in the emergency department: challenges and solutions. Emerg Med 2015; 7: 39-44. Doi: 10.2147/OAEM.S73684
Belay Y, Yirdaw K, Enawgaw B. Tumor lysis syndrome in patients with hematological malignancies. J Oncol 2017. doi: 10.1155/2017/9684909
Burgi G, Berutti D, Manzanares W. Síndrome de lisis tumoral en terapia intensiva: encare diagnóstico y terapéutico. Medicina Intensiva 2011; 35(3): 170-178. DOI: 10.1016/j. medin.2010.07.014
Saeed F, Ali M, Ashraf M, Vadsaria K, Siddiqui D. Síndrome de lisis tumoral en niños con cánceres hematológicos: experiencia en un hospital de atención terciaria en Karachi. J Pak Med Asoc 2018; 68(11): 1625-1630.
Kollathodi S, Parameswaran K, Madhavan L, Kuruvilla S. Hematological malignancies presenting as spontaneous tumor lysis syndrome: A case series. J Family Med Prim Care 2018; 7(5): 1116-1119. doi: 10.4103/jfmpc.jfmpc_171_18
Gogia A, Raina V, Iqbal N, Murugan V. Síndrome de lisis tumoral espontánea en un paciente con leucemia linfocítica crónica. Indio J Med Paediatr Oncol 2014; 35(1): 120. doi: 10.4103 / 0971-5851.133740
Adeyinka A, Bashir K. Síndrome de lisis tumoral. StatPearls [Internet]. Brooklyn: 2020. StatPearls Publishing LLC. Disponible en: www.ncbi.nlm.nih.gov › books › NBK518985
Caravaca-Fontan F, Martínez-Sáenz O, Pampa-Saico S, Olmedo M, Gomis A, Garrido P. Síndrome de lisis tumoral en neoplasias sólidas: características clínicas y pronóstico. Medicina Clínica 2017; 148(3): 121-124. DOI: 10.1016/j. medcli.2016.10.040
Calvo-Villas J. Síndrome de lisis tumoral. Medicina Clínica 2019; 152(10): 397-404. DOI: 10.1016/j.medcli. 2018.10.029
McBride A, Trifilio S, Baxter N, Gregory T, Howard S. Managing tumor lysis syndrome in the era of novel cancer therapies. J Adv Pract Oncol 2017; 8: 705-720.
Sánchez-Tatay V, López-Castilla J, Carmona-Ponce J, Pérez- Hurtado J, Quiroga-Cantero E, Loscertales-Abril M. Rasburicasa versus alopurinol como tratamiento de la hiperuricemia en el síndrome de lisis tumoral. Anales de Pediatría 2010; 72(2): 103-110. DOI: 10.1016/j.anpedi.2009.10.011
Mirrakhimov AE, Voore P, Khan M, Ali AM. Tumor lysis syndrome: A clinical review. World J Crit Care Med 2015; 4(2): 130-138.
Worcester EM, Coe FL. Clinical practice. Calcium kidney stones. N Engl J Med 2010; 363: 954-963.
Maxwell AP, Linden K, O’Donnell S, Hamilton PK, McVeigh GE. Management of hyperkalaemia. J R Coll Physicians Edinb 2013; 43: 246-251.