Urology Annals

CASE REPORT
Year
: 2020  |  Volume : 12  |  Issue : 2  |  Page : 193--195

Renal sinus angiomyolipoma: A rare case


Abhimanyu Gupta, Shivam Priyadarshi, Nachiket Vyas 
 Department of Urology, SMS Hospital, Jaipur, Rajasthan, India

Correspondence Address:
Prof. Nachiket Vyas
Department of Urology, SMS Hospital, Jaipur, Rajasthan
India

Angiomyolipoma (AML) consists of <10% of all renal tumors and is the most common benign mesenchymal neoplasm of the kidney. It arises from the renal cortex and extends toward perirenal fat. Fat-poor AML as well as those arising from rare locations may pose diagnostic difficulties. In our case, we report a rare presentation of this tumor arising from the renal sinus extending toward the pelvis thereby leading to an alternative diagnosis of transitional cell carcinoma of renal pelvis.


How to cite this article:
Gupta A, Priyadarshi S, Vyas N. Renal sinus angiomyolipoma: A rare case.Urol Ann 2020;12:193-195


How to cite this URL:
Gupta A, Priyadarshi S, Vyas N. Renal sinus angiomyolipoma: A rare case. Urol Ann [serial online] 2020 [cited 2020 Oct 19 ];12:193-195
Available from: https://www.urologyannals.com/article.asp?issn=0974-7796;year=2020;volume=12;issue=2;spage=193;epage=195;aulast=Gupta;type=0