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A Rare Case of Renal Sarcoma Mimicking Metastatic Osteosarcoma

  • Rennen Haramaty
  • , Eddie Fridman
  • , Ignat Schwartz
  • , Haim Huri
  • , Yoram Mor
  • , Alon Lazarovich*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Pediatric renal sarcomas are exceedingly rare entities that present diagnostic challenges. We report a remarkable case of a 14-month-old female with an 8 cm right renal mass, accompanied by disseminated bone metastases, posing intricate clinical and histopathological dilemmas. Initial suspicion leaned towards clear cell sarcoma of the kidney (CCSK), however, subsequent histological examination post-chemotherapy revealed high-grade osteosarcoma and further differential considerations arose, including primary renal osteosarcoma and osseous osteosarcoma with secondary renal involvement. Despite inconclusive histology, treatment proceeded with the UH1 chemotherapy protocol for CCSK, incorporating high-dose Methotrexate for potential osteosarcoma, and the patient demonstrated a favorable response to therapy.

Original languageEnglish
Pages (from-to)e17-e20
JournalUrology
Volume190
DOIs
StatePublished - Aug 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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