1IntroductionSolitary fibrous tumors (SFT) are rare mesenchymal tumors that account for approximately 2% of all soft tissue neoplasms[1]. The etiology of SFTs is unknown; however, they are typically slow-growing tumors with a favorable prognosis. These soft tissue tumors can be found in any part of the body, with the thorax identified as the most common site. Renal SFT are relatively rare, with only 105 cases of renal SFTs reported in the literature[1]. The clinical presentation of renal SFT varies widely, ranging from asymptomatic incidental findings to abdominal discomfort, hematuria, renal masses, and large abdominal masses. Furthermore, owing to the nonspecific nature of radiologic features, renal SFT are frequently misdiagnosed and managed as Renal Cell Carcinoma. Surgical resection remains the primary treatment modality for localized renal SFT and, yields favorable outcomes in most cases.