Publication:
Retroperitoneal fibrosis due to malignancy: A case report

dc.contributor.authorsErton M.L., Ilker Y.N., Ceyhan N., Akdas A.
dc.date.accessioned2022-03-15T01:53:04Z
dc.date.accessioned2026-01-11T10:26:13Z
dc.date.available2022-03-15T01:53:04Z
dc.date.issued1995
dc.description.abstractRetroperitoneal fibrosis is idiopathic in two thirds of cases and is found most commonly as an isolated fibrotic plaque centered over the lumbar spine and entrapping one or both ureters. It has been postulated that fibrosis in the idiopathic cases results from a hypersensitivity reaction to antigens leaking into the retroperitoneum from atheromatous plaques in the aorta or common iliac arteries. In the remaining one third of cases, causes include ergot-derivative drugs, retroperitoneal haemorrhage or urine extravasation, and a desmoplastic response to a variety of tumours. © 1995 Akadémiai Kiadó.
dc.identifier.doi10.1007/BF02551311
dc.identifier.issn3011623
dc.identifier.pubmed7591570
dc.identifier.urihttps://hdl.handle.net/11424/246246
dc.language.isoeng
dc.publisherKluwer Academic Publishers
dc.relation.ispartofInternational Urology and Nephrology
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleRetroperitoneal fibrosis due to malignancy: A case report
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage150
oaire.citation.issue2
oaire.citation.startPage147
oaire.citation.titleInternational Urology and Nephrology
oaire.citation.volume27

Files