acquired cystic disease-associated renal cell carcinoma
http://purl.obolibrary.org/obo/MONDO_0018449
Acquired cystic disease-associated renal cell carcinoma is a rare subtype of renal cell carcinoma, ocurring in the context of end-stage kidney disease and acquired cystic kidney disease, characterized by a usually well circumscribed, solid, multifocal, bilateral tumor with inter- or intracellular microlumen formation (leading to cribiform architecture). Tumors are often diagnosed incidentally in early stages, although complications caused by renal cysts (dull flank or abdominal pain, fever) or renal parenchymal bleeding may mask the underlying neoplastic process. Most have an indolent behavior. [ Orphanet:404514 ]
Term info
- UMLS:CN226194 (MONDO:equivalentTo)
- Orphanet:404514 (MONDO:equivalentTo)
- NCIT:C157718 (MONDO:equivalentTo)
ordo_disease
Acquired cystic disease-associated renal cell carcinoma is a rare subtype of renal cell carcinoma, ocurring in the context of end-stage kidney disease and acquired cystic kidney disease, characterized by a usually well circumscribed, solid, multifocal, bilateral tumor with inter- or intracellular microlumen formation (leading to cribiform architecture). Tumors are often diagnosed incidentally in early stages, although complications caused by renal cysts (dull flank or abdominal pain, fever) or renal parenchymal bleeding may mask the underlying neoplastic process. Most have an indolent behavior.
http://linkedlifedata.com/resource/umls/id/CN226194, http://purl.obolibrary.org/obo/Orphanet_404514, http://purl.obolibrary.org/obo/NCIT_C157718
MONDO:0018449