Spontaneous tumor lysis syndrome

Authors

  • Victoria Augustín Bandera Servicio de Medicina Interna. Hospital Costa del Sol. Marbella (Málaga). España
  • María Ángeles Villena-Ruiz Servicio de Medicina Interna. Hospital Costa del Sol. Marbella (Málaga). España
  • Francisco Granados Pacheco Servicio de Anatomía Patológica. Hospital Costa del Sol. Marbella (Málaga). España
  • Luis Robles Cabeza Servicio de Anatomía Patológica. Hospital Costa del Sol. Marbella (Málaga). España
  • Josefa Andrea Aguilar García Servicio de Medicina Interna. Hospital Costa del Sol. Marbella (Málaga). España

DOI:

https://doi.org/10.32818/reccmi.a5n2a4

Keywords:

kidney failure, hyperuricemia, tumor lysis.

Abstract

Tumor lysis syndrome is a complication that usually occurs at the beginning of antineoplastic treatment, being the cases of spontaneous appearance very rare and even less associated with solid tumors.
We present the case of a 69-year-old male with the constitutional syndrome and the presence of multiple hepatic micronodules, evolving rapidly and progressively to a spontaneous tumor lysis syndrome.

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References

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Published

2020-08-31

How to Cite

1.
Augustín Bandera V, Villena-Ruiz M Ángeles, Granados Pacheco F, Robles Cabeza L, Aguilar García JA. Spontaneous tumor lysis syndrome. Rev Esp Casos Clin Med Intern [Internet]. 2020 Aug. 31 [cited 2024 Jul. 22];5(2):65-7. Available from: https://www.reccmi.com/RECCMI/article/view/494