“…Furthermore, paraneoplastic syndromes such as hypercalcemia, leukocytosis, and thrombocytosis may be associated with RSCC [ 3 ]. The main differential diagnosis of renal SCC is XGP (xanthogranulomatous), a structure also associated with renal calculi that leads to hydronephrosis and forms an inflammatory mass that destroy renal parenchyma, mimicking malignancy in addition to primary and secondary renal neoplasms [ 14 , 15 ]. It is highly possible that by the time of diagnosis, the tumor has invaded the renal parenchyma or adjacent tissues, and owing to its aggressive behavior, SCC often presents at stage-pT3 or higher and may spread to regional lymph nodes, lungs, and the liver, and rarely to bones [ 3 ].…”