papillary adenocarcinoma renal cell adenocarcinoma papillary renal cell carcinoma DOID:4465 EFO:0000640 GARD:0009572 GARD:0009575 HPRCC ICD10:C64 MONDO:0017884 NCIT:C6975 OMIM:605074 ONCOTREE:PRCC Orphanet:319298 Orphanet:47044 Papillary renal cell carcinoma is 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. RCCP RCCP1 SCTID:733608000 UMLS:C1306837 UMLS:C1336078 UMLS:CN205129 chromophil RCC chromophil carcinoma of kidney chromophil carcinoma of the kidney chromophil renal cell carcinoma https://rarediseases.info.nih.gov/diseases/9572/papillary-renal-cell-carcinoma papillary (chromophil) renal cell carcinoma papillary kidney carcinoma papillary renal carcinoma, malignant - (subtype) papillary renal cell adenocarcinoma papillary renal cell cancer papillary renal cell carcinoma papillary renal cell carcinoma, bilateral - (subtype) papillary renal cell carcinoma, familial - (subtype) papillary renal cell carcinoma, multiple - (subtype) papillary renal cell carcinoma, sporadic - (subtype) renal adenocarcinoma renal cell carcinoma, papillary, 1 renal cell carcinoma, papillary, type 1 sporadic papillary renal cell carcinoma inherited renal cancer-predisposing syndrome