“…Accounting for 70% of all RCCs, the clear cell subtype is the most common, followed by papillary (10%-15%), chromophobe (5%), unclassified (4%), and other rare subtypes (<1%), including multilocular cystic, collecting duct, medullary, mucinous tubular and spindle cell, neuroblastoma-associated, Xp11.2 translocation-TFE3, and hybrid oncocytic tumor [associated with BirtHogg-Dube´(BHD)] [8-10]. Subtyping has prognostic significance, as clear cell, collecting duct, papillary type 2, and medullary can be aggressive, while papillary type 1, chromophobe, and multilocular cystic are more indolent [8,[10][11][12]. Subtyping can potentially alter management as well; while surgical resection remains the standard of treatment for RCC, in patients who are elderly, have multiple co-morbidities, or are otherwise poor surgical candidates, preoperative knowledge that a tumor is more likely to be a less aggressive RCC subtype may lead to consideration of ablation therapy or surveillance, rather than surgery.…”