Indian Journal of Urology
CASE REPORT
Year
: 2007  |  Volume : 23  |  Issue : 3  |  Page : 319--320

Adrenal angiomyolipoma: A rare entity


Rajesh Godara1, MG Vashist1, Sham L Singla1, Pradeep Garg1, Jyotsena Sen2, SK Mathur3, Anshu Gupta3 
1 Department of Surgery, Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India
2 Department of Radiodiagnosis, Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India
3 Department of Pathology, Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India

Correspondence Address:
Rajesh Godara
58/9J, Medical Enclave, Rohtak, Haryana - 124 001
India

Angiomyolipoma is apparently a part of a family of neoplasms that derive from perivascular epitheloid cells. It is a rare mesenchymal tumor, usually found in the kidney. Extrarenal angiomyolipoma is uncommon and the most common extrarenal site is the liver. Only two cases of adrenal angiomyolipoma are reported in English literature. Authors wish to add one more case to world literature. Because of its large size and symptomatic presentation of extremely rare tumor merits documentation.


How to cite this article:
Godara R, Vashist M G, Singla SL, Garg P, Sen J, Mathur S K, Gupta A. Adrenal angiomyolipoma: A rare entity.Indian J Urol 2007;23:319-320


How to cite this URL:
Godara R, Vashist M G, Singla SL, Garg P, Sen J, Mathur S K, Gupta A. Adrenal angiomyolipoma: A rare entity. Indian J Urol [serial online] 2007 [cited 2022 Sep 30 ];23:319-320
Available from: https://www.indianjurol.com/article.asp?issn=0970-1591;year=2007;volume=23;issue=3;spage=319;epage=320;aulast=Godara;type=0