ISSN 2149-3235 | E-ISSN 2149-3057
Case Report
Renal angiomyoadenomatous tumour
1 Department of Pathology, Government Medical College, Thrissur, Kerala, India  
2 Department of Urology, Government Medical College, Thrissur, Kerala, India  
Turk J Urol 2017; 43: 378-382
DOI: 10.5152/tud.2017.32067
Key Words: Labrynthine vascular channels; rare renal tumour; renal angiomyoadenomatous tumour
Abstract

Renal angiomyoadenomatous tumour is a newly described rare neoplasm. This tumour is characterised microscopically by admixture of three components- epithelial cells arranged in tubules and nests, angiomyomatous stroma and capillary sized interconnecting vascular channels in close association with the epithelial cell clusters. Microscopically it has wide range of differential diagnoses which include mixed epithelial and stromal tumour of kidney, angiomyolipoma and clear cell renal cell carcinoma with angiomyolipomatous/angiomyoadenomatous areas. Renal angiomyoadenomatous tumour should be differentiated from these tumours. Till now, only 10 cases have been reported in English medical literature. Here, we are reporting a case of renal angiomyoadenomatous tumour in a 29 year- old female patient who presented with hematuria and low backache and describing its main features so as to differentiate this entity from other renal tumours. To the best of our knowledge, this is the first case to be reported from India.

 

 

Cite this article as: Jayalakshmy PS, Jose M, Feroze M, Kumar RK. Renal Angiomyoadenomatous tumour. Turk J Urol 2017; 43: 378-82

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