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

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,...

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Bibliographic Details
Main Authors: Hasan Haydar, Mouhammed Sleiay, Mohammed Alqreea, Ahmad Almohamed, Doaa Alrajab, Malak alsaleh, Mohamad Yasin Lutfi
Format: Article
Language:English
Published: Elsevier 2024-05-01
Series:Urology Case Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2214442024000597
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Summary: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
ISSN:2214-4420