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Spontaneous Tumor Lysis Syndrome in a Case of Hepatocellular Carcinoma with Sarcomatoid Differentiation

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Abstract

Sarcomatoid hepatocellular carcinoma is a rare histologic variant of primary liver cancer comprising of malignant spindle cells and typical hepatocellular carcinoma (HCC). In terms of clinical presentation, they usually exhibit extensive tumor burden due to their larger size and a metastatic disease at the time of diagnosis as compared to conventional HCC. Tumor lysis syndrome is an oncological emergency, usually seen after cytotoxic chemotherapy in haematological malignancies. Here, we highlight a case of 76-year old male with no comorbidities, presenting with an excruciating backache and a paravertebral soft tissue mass and multiple osteolytic lesions, was clinically suspected to be a plasma cell neoplasm. On further evaluation, the patient was diagnosed of a sarcomatoid variant of hepatocellular carcinoma. This report showcases multiple rare findings by the presence of non-specific symptoms, non-cirrhotic liver, normal serum alpha protein levels and the occurrence of a spontaneous tumor lysis syndrome in a solid malignancy.

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The authors received no financial support for the research, authorship, and/or publication of this article.

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Contributions

Conceptualization: RC, AV, SR, JS, MAO.

Data curation: RC, JS.

Project administration: AV, SR, JS.

Writing-original draft: RC, MAO.

Writing-review & editing: RC, MAO.

Approval of final manuscript: RC, AV, SR, JS, MAO.

Corresponding author

Correspondence to Md Ali Osama.

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Chhabra, R., Vidushi, A., Rajpurohit, S. et al. Spontaneous Tumor Lysis Syndrome in a Case of Hepatocellular Carcinoma with Sarcomatoid Differentiation. Indian J Surg Oncol 15, 370–374 (2024). https://doi.org/10.1007/s13193-024-01895-0

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  • DOI: https://doi.org/10.1007/s13193-024-01895-0

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