papillary adenocarcinoma renal cell adenocarcinoma papillary renal cell carcinoma https://rarediseases.info.nih.gov/diseases/9572/papillary-renal-cell-carcinoma https://www.malacards.org/card/papillary_renal_cell_carcinoma Orphanet:319298 papillary renal cell adenocarcinoma GARD:0009572 NCIT:C6975 A rare subtype of renal cell carcinoma, arising from the renal tubular epithelium and showing a papillary growth pattern, which typically manifests with hematuria, flank pain, palpable abdominal mass or nonspecific symptoms, such as fatigue, weight loss or fever. Symptoms related to metastatic spread, such as bone pain or persistent cough, are frequently associated since early diagnosis is not common. It is typically multifocal, bilateral, and in most cases sporadic, although different hereditary syndromes, such as Hereditary leiomyoma renal cell carcinoma, Birt-Hogg-DubC) syndrome and Tuberous sclerosis, may predispose to the development of papillary renal cell carcinoma. renal cell carcinoma, papillary, 1 papillary (chromophil) renal cell carcinoma papillary renal cell carcinoma, multiple - (subtype) papillary renal cell carcinoma RCCP renal adenocarcinoma renal cell carcinoma, papillary, type 1 papillary renal cell carcinoma, bilateral - (subtype) SCTID:733608000 chromophil carcinoma of the kidney DOID:4465 papillary renal carcinoma, malignant - (subtype) MONDO:0017884 chromophil carcinoma of kidney RCCP1 papillary renal cell carcinoma, sporadic - (subtype) ONCOTREE:PRCC chromophil RCC EFO:0000640 chromophil renal cell carcinoma HPRCC papillary renal cell carcinoma, familial - (subtype) MEDGEN:266300 UMLS:C1306837 papillary renal cell cancer obsolete inherited renal cancer-predisposing syndrome