Spontaneous Tumor Lysis Syndrome Revealing Advanced Ovarian Carcinoma: From Oncologic Emergency to Complete Pathologic Response

Tumor lysis syndrome (TLS) is an oncologic emergency characterized by metabolic abnormalities resulting from rapid tumor cell breakdown. It is most frequently observed following cytotoxic therapy in hematologic malignancies and is rarely encountered spontaneously in solid tumors. Spontaneous TLS associated with ovarian carcinoma remains exceptionally uncommon. A 53-year-old woman with no pertinent medical history presented with progressive abdominal distension, dyspnea, and oliguria. Laboratory evaluation demonstrated acute kidney injury with a serum creatinine of 4.09 mg/dL, accompanied by hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia, fulfilling the Cairo-Bishop criteria for clinical TLS. Computed tomography (CT) revealed massive ascites and a 16.2 × 15 × 15 cm pelvic mass without evidence of obstructive uropathy. Ascitic fluid cytology demonstrated metastatic carcinoma. Tumor markers showed a cancer antigen (CA)-125 level of 445 U/mL and a CA-125:carcinoembryonic antigen ratio greater than 25, strongly supporting a gynecologic primary malignancy. In the absence of recent chemotherapy or other precipitating factors, spontaneous TLS secondary to previously undiagnosed ovarian carcinoma was diagnosed. The patient was treated with aggressive intravenous hydration, rasburicase, electrolyte correction, and close multidisciplinary monitoring, resulting in rapid normalization of metabolic abnormalities and recovery of renal function without dialysis. Following stabilization, the patient underwent neoadjuvant carboplatin-paclitaxel chemotherapy followed by interval cytoreductive surgery. Histopathologic examination demonstrated a complete pathologic response, with no residual invasive carcinoma. Follow-up positron emission tomography/CT imaging showed no evidence of residual or metastatic disease, and CA-125 normalized to 5.2 U/mL. This case highlights spontaneous TLS as a rare initial manifestation of advanced ovarian carcinoma and emphasizes the importance of early recognition and prompt intervention. Timely management may reverse life-threatening metabolic complications, facilitate definitive oncologic treatment, and result in favorable long-term outcomes.

Authors

Publication Details

Journal
Cureus
Published
2026-07-23
DOI
https://doi.org/10.7759/cureus.113241
Primary Topic
Methemoglobinemia and Tumor Lysis Syndrome
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Spontaneous Tumor Lysis Syndrome Revealing Advanced Ovarian Carcinoma: From Oncologic Emergency to Complete Pathologic Response

John-Luke Rivera, Milton Carrero Quinones, C Mendez Vargas, Madeline Guerrero-Gonzalez et al.
Cureus
Methemoglobinemia and Tumor Lysis Syndrome
article

Spontaneous Tumor Lysis Syndrome Revealing Advanced Ovarian Carcinoma: From Oncologic Emergency to Complete Pathologic Response

John-Luke Rivera, Milton Carrero Quinones, C Mendez Vargas, Madeline Guerrero-Gonzalez, Alejandra P Rivera Caro, Eden Ocana-Vazquez, Santa Merle
article en

Abstract

Tumor lysis syndrome (TLS) is an oncologic emergency characterized by metabolic abnormalities resulting from rapid tumor cell breakdown. It is most frequently observed following cytotoxic therapy in hematologic malignancies and is rarely encountered spontaneously in solid tumors. Spontaneous TLS associated with ovarian carcinoma remains exceptionally uncommon. A 53-year-old woman with no pertinent medical history presented with progressive abdominal distension, dyspnea, and oliguria. Laboratory evaluation demonstrated acute kidney injury with a serum creatinine of 4.09 mg/dL, accompanied by hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia, fulfilling the Cairo-Bishop criteria for clinical TLS. Computed tomography (CT) revealed massive ascites and a 16.2 × 15 × 15 cm pelvic mass without evidence of obstructive uropathy. Ascitic fluid cytology demonstrated metastatic carcinoma. Tumor markers showed a cancer antigen (CA)-125 level of 445 U/mL and a CA-125:carcinoembryonic antigen ratio greater than 25, strongly supporting a gynecologic primary malignancy. In the absence of recent chemotherapy or other precipitating factors, spontaneous TLS secondary to previously undiagnosed ovarian carcinoma was diagnosed. The patient was treated with aggressive intravenous hydration, rasburicase, electrolyte correction, and close multidisciplinary monitoring, resulting in rapid normalization of metabolic abnormalities and recovery of renal function without dialysis. Following stabilization, the patient underwent neoadjuvant carboplatin-paclitaxel chemotherapy followed by interval cytoreductive surgery. Histopathologic examination demonstrated a complete pathologic response, with no residual invasive carcinoma. Follow-up positron emission tomography/CT imaging showed no evidence of residual or metastatic disease, and CA-125 normalized to 5.2 U/mL. This case highlights spontaneous TLS as a rare initial manifestation of advanced ovarian carcinoma and emphasizes the importance of early recognition and prompt intervention. Timely management may reverse life-threatening metabolic complications, facilitate definitive oncologic treatment, and result in favorable long-term outcomes.

Cureus
Good health and well-being
Openalex Percentile: Top 10%
Methemoglobinemia and Tumor Lysis Syndrome
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.