loading...| Preferred Name |
papillary renal cell carcinoma |
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| Synonyms |
papillary renal cell adenocarcinoma HPRCC papillary renal cell cancer papillary (chromophil) renal cell carcinoma renal cell carcinoma, papillary, type 1 papillary kidney carcinoma chromophil carcinoma of kidney chromophil renal cell carcinoma sporadic papillary renal cell carcinoma chromophil carcinoma of the kidney papillary renal cell carcinoma papillary renal cell carcinoma, familial - (subtype) papillary renal carcinoma, malignant - (subtype) RCCP1 RCCP renal adenocarcinoma papillary renal cell carcinoma, sporadic - (subtype) renal cell carcinoma, papillary, 1 chromophil RCC papillary renal cell carcinoma, multiple - (subtype) papillary renal cell carcinoma, bilateral - (subtype) |
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| Definitions |
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. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0017884 |
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| database_cross_reference |
GARD:9572 ONCOTREE:PRCC Orphanet:319298 EFO:0000640 DOID:4465 UMLS:C1306837 NCIT:C6975 SCTID:733608000 |
|
| definition |
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. |
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| exactMatch |
http://purl.obolibrary.org/obo/NCIT_C6975 http://purl.obolibrary.org/obo/Orphanet_319298 http://linkedlifedata.com/resource/umls/id/C1306837 |
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| has_exact_synonym |
papillary renal cell adenocarcinoma HPRCC papillary renal cell cancer papillary (chromophil) renal cell carcinoma renal cell carcinoma, papillary, type 1 papillary kidney carcinoma chromophil carcinoma of kidney chromophil renal cell carcinoma sporadic papillary renal cell carcinoma chromophil carcinoma of the kidney papillary renal cell carcinoma |
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| has_related_synonym |
papillary renal cell carcinoma, familial - (subtype) papillary renal carcinoma, malignant - (subtype) RCCP1 RCCP renal adenocarcinoma papillary renal cell carcinoma, sporadic - (subtype) renal cell carcinoma, papillary, 1 chromophil RCC papillary renal cell carcinoma, multiple - (subtype) papillary renal cell carcinoma, bilateral - (subtype) |
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| id |
MONDO:0017884 |
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| in_subset |
http://purl.obolibrary.org/obo/mondo#ordo_disease http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#nord_rare http://purl.obolibrary.org/obo/mondo#orphanet_rare |
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| label |
papillary renal cell carcinoma |
|
| notation |
MONDO:0017884 |
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| prefLabel |
papillary renal cell carcinoma |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/9572/papillary-renal-cell-carcinoma |
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| treeView | ||
| excluded subClassOf | ||
| subClassOf |