“…Histologic presentation reveals tumors with extensive squamous differentiation, and the landmarks are pearl formation, intercellular bridges, and keratotic cellular debris and the conspicuous presence of keratinizing squamous metaplasia of the adjacent flattened urothelium, especially if associated with dysplasia, supports a diagnosis of primary SCC of the renal pelvis which is rare. [6,7] Existing literature and previous studies reveal that metastasis is sporadic and is usually a sign of end stage disease with a poor prognosis as Nativ, et al in their study have divided renal SCC in three groups, reported 1 and 2 year survival rates of locally invasive renal SCC 33% and 22% respectively. [8] The current modality of treatment of RSCC is primarily by Nephrectomy, [1,8,9] to rephrase Nephrectomy with or without ureterectomy even in the presence of distant metastasis.…”