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CASE REPORT
Management of tumour lysis syndrome during first-line palliative chemotherapy for high-volume colorectal cancer
  1. Helena S Gouveia1,
  2. Sílvia O Lopes2,
  3. Ana Luísa Faria1
  1. 1Medical Oncology Department, Centro Hospitalar de Entre Douro e Vouga, EPE, Santa Maria da Feira, Portugal
  2. 2Medical Oncology Department, Centro Hospitalar do Porto, Porto, Portugal
  1. Correspondence to Dr Helena S Gouveia, helena.gouveia{at}chedv.min-saude.pt

Summary

Tumour lysis syndrome (TLS) is a rare oncological emergency in solid tumours. Because it is associated with bad short-term prognosis, early recognition and treatment are mandatory. This case refers to a middle-aged woman who presented with stage IV colon cancer, with massive hepatic involvement. After three cycles of first-line FOLFOX (folinic acid, 5-fluorouracil and oxaliplatin), she developed acute kidney injury and hyperkalaemia that did not respond to standard measures. High suspicion of TLS prompted further corroborating investigations and early intensive care unit admission. With vigorous hydration and allopurinol, TLS completely resolved and the patient was discharged. Prophylaxis of subsequent TLS recurrence was complicated by biopsy-proven neutrophilic vasculitis secondary to allopurinol. Prevention of TLS with hydration and rasburicase was performed prior to each subsequent cycle of chemotherapy. This case report is intended to highlight risk factors for TLS in solid tumours and focus on treatment and secondary prophylaxis of TLS.

  • chemotherapy
  • colon cancer
  • acute renal failure
  • fluid electrolyte and acid-base disturbances

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Footnotes

  • HS and SOL contributed equally.

  • Contributors HSG and SOL were responsible for writing the article. HSG was responsible for choosing the clinical case for its scientific relevance and performing the systematic literature review. SOL— who was the attending physician—obtained informed consent and was responsible for choosing images and captions in the article. ALF was responsible for giving valuable input in writing the article and steering contents in the discussion.

  • Funding This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

  • Competing interests None declared.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.