A 28-year-old patient with tuberous sclerosis associated with renal angiomyolipoma:A rare case report and literature review

Urol Case Rep. 2024 Mar 13:54:102705. doi: 10.1016/j.eucr.2024.102705. eCollection 2024 May.

Abstract

Tuberous sclerosis complex (TSC) is a genetically inherited disorder distinguished by the development of numerous benign neoplasms across multiple organ systems. Renal angiomyolipoma represents 0.3% of all primary renal tumors and are classified as benign mixed mesenchymal neoplasms. In this report, we reported the clinical presentation of a 28-year-old individual who was received by the department of urology. The patient was admitted presenting with asymptomatic, macroscopic hematuria that had been ongoing for a period of 10 days. Subsequent diagnostic evaluations revealed an association between the presenting urinary condition and tuberous sclerosis complex with a concurrent renal angiomyolipom.

Keywords: Renal angiomyolipoma; Renal mass; TSC; Tubersclerosis.

Publication types

  • Case Reports