DOI: 10.36347/sasjm.2024.v10i06.018

Pages: 564-566

Rhabdoid tumors of the kidney are rare childhood renal neoplasms, extremely aggressive and typically carrying a grim prognosis, its common correlation with primary or metastatic central nervous system (CNS) lesions these tumors primarily impact infants, with an average age of onset at 11 months (ranging from birth to 9 years [1]. Initially thought to be a sarcomatoid subtype of Wilms' tumor, it is now recognized as a separate pathological entity [2]. At the beginning of the illness, typical clinical signs in clued hematurie, abdominal pain, and abdominal swelling. Imaging studies are the primary method used to diagnose renal masses in children.