Ossifying renal tumor of infancy: A case report

Abstract

Ossifying Renal Tumor of Infancy (ORTI) represents an extremely rare and benign renal neoplasm, with limited cases published in the literature. Predominantly characterized by painless and intermittent gross hematuria, the diagnostic evaluation is effectively facilitated through ultrasound, computed tomography, and magnetic resonance imaging. Despite progress, its etiology has not yet been elucidated. We report an additional case with an unusual clinical presentation.

Keywords

• Ossifying renal tumor of infancy (ORTI)
• Renal tumor
• Hematuria
• Infant