Abstract
The Tumor Lysis Syndrome is an oncological emergency, caused by destruction of the tumor cell, spontaneously or secondary to chemotherapy, generating release of the intracellular content into the bloodstream. Producing hyperuricemia, hyperphosphatemia, hypocalcemia and hyperkalemia. For its diagnosis, a high degree of suspicion and the Cairo-Bishop and Howard criteria must be applied. A case of a 35-year-old patient is presented with a history of stage IIC retroperitoneal non-gonadal seminoma. He was admitted from an outpatient clinic due to intolerance to the oral route, dehydration and paresthesia in the lower limbs, hyperkalemia, hypocalcemia and hyperuricemia, in addition, elevated serum creatinine. It was considered a diagnosis of tumor lysis syndrome; it was treated with aggressive fluid therapy at a dose of 2-3 L/m2/day of normal saline solution. In addition, rasburicase it was indicated and electrolyte disturbances were corrected. Once renal function was above 60 mL/min/1,73 m3, cytoreductive treatment with cisplatin, etoposide, and bleomycin it was started. The importance of having a diagnostic suspicion in cancer patients concluded, even in low-risk neoplasms, in addition, it is highlighted that, in the literature reviews, its incidence is subject to case reports.References
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