Tumor lysis syndrome (TLS) is an oncologic emergency characterized by severe metabolic derangements resulting from rapid tumor cell breakdown. We present the case of a 66-year-old man with extensive-stage small cell lung cancer (SCLC) involving the mediastinum, pleura, and left upper lobe, who developed TLS shortly after initiation of cisplatin-etoposide chemotherapy. Laboratory evaluation demonstrated hyperuricemia, hyperkalemia, hyperphosphatemia, syndrome of inappropriate antidiuretic hormone secretion (SIADH)-related hyponatremia, and acute kidney injury, consistent with TLS. Imaging revealed extensive intrathoracic disease with a large left pleural effusion and mediastinal involvement. The patient required aggressive electrolyte management and close monitoring following chemotherapy initiation. This case emphasizes the importance of maintaining clinical suspicion for TLS in patients with bulky SCLC receiving cytotoxic therapy and highlights the need for early recognition and prompt intervention.
Figueroa et al. (Mon,) studied this question.