Qap (Anatomical Pathology) 

QAP Peer Review

AP223
Case History: M/80, 5 cm multicystic renal mass
Intended diagnosis: Tubulocystic carcinoma with a component of papillary renal cell carcinoma. Contributed by:MST
Code Diagnosis Comment Score
anonymous Papillary renal cell carcinoma (100%) nil  90
anonymous papillary renal cell carcinoma nil  90
anonymous Renal cell carcinoma, mixed pattern (conventional & papillary) (100%) If there is clinical history of end stage renal failure, the diagnosis would be acquired cystic disease associated Renal cell carcinoma  90
anonymous Papillary renal cell carcinoma (associated with acquired renal cystic disease) Correlate with clinical finding of presence of end-stage renal disease.  90
anonymous Tubulocystic carcinoma with a component of papillary renal cell carcinoma, Furhman nuclear grade 3 out of 4. 100% nil  100
anonymous Renal cell carcinoma.(100%) nil  80
anonymous Kidney - composite Papillary carcinoma and Tubulocystic carcinoma 100% nil  100
anonymous Papillary renal cell carcinoma nil  90
anonymous PAPILLARY RENAL CELL CARCINOMA TYPE II NUCLEAR GRADE 2 100% nil  90
anonymous Renal cell carcinoma, papillary variant. nil  90
anonymous Kidney - Renal cell carcinoma, grade 2 (Fuhrman) The overall features are suggestive of renal cell carcinoma complicating acquired cystic disease secondary to chronic dialysis. The prognosis is better than sporadic cases.  80
anonymous Renal cell carcinoma There are focal cystic and papillary areas. Suggest correlation with clinical history for evidence of acquired cystic disease of kidney and history of renal dialysis.  90
anonymous Multilocular cystic renal cell carcinoma (100% probability) nil  80
anonymous Papillary renal cell carcinoma (100%) nil  90
anonymous Tubulocytic carcinoma (100%). Immunohistochemical stain for CK7.  95