{Reference Type}: Case Reports
{Title}: A 28-year-old patient with tuberous sclerosis associated with renal angiomyolipoma:A rare case report and literature review.
{Author}: Haydar H;Sleiay M;Alqreea M;Almohamed A;Alrajab D;Alsaleh M;Lutfi MY;
{Journal}: Urol Case Rep
{Volume}: 54
{Issue}: 0
{Year}: 2024 May
暂无{DOI}: 10.1016/j.eucr.2024.102705
{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.