Unilateral autosomal dominant polycystic kidney disease with co-existent renal cell carcinoma: A rare entity

Bilateral ADPKD is a well-known entity, but there are only a few reports on unilateral ADPKD in adults, most of which had associated contralateral agenesis. Further rare is the development of RCC in unilateral ADPKD. We present an exceedingly rare case of true unilateral ADPKD with normal contralate...

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Bibliographic Details
Main Authors: Anupama Tandon, Mohd Shuaib Qureshi, Irfan Ahmad, Usha Rani Singh, Shuchi Bhatt
Format: Article
Language:English
Published: SpringerOpen 2018-03-01
Series:The Egyptian Journal of Radiology and Nuclear Medicine
Online Access:http://www.sciencedirect.com/science/article/pii/S0378603X17302097