Article:
Rare solitary fibrous tumour of kidney

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorPathak, Tilak Bahadur
dc.contributor.authorNepal, Umesh
dc.creator.affiliationB.P. Koirala Memorial Cancer Hospital, Bharatpur, Chitwan, Nepal.
dc.creator.affiliationB.P. Koirala Memorial Cancer Hospital, Bharatpur, Chitwan, Nepal.
dc.date.accessioned2026-10-29T07:20:03Z
dc.date.available2026-10-29T07:20:03Z
dc.date.issued2013
dc.description.abstractAbstract A solitary fibrous tumour (SFT) is an unusual spindle cell neoplasm. It frequently arises from the serosal surface of pleural cavity but has recently been described in diverse extrapleural sites. Urogenital localization is rare and only 36 cases of SFTs of the kidney have been described on published report. We report a case of a large SFT clinically and radiologically thought to be renal cell carcinoma arising in the kidney of a 30- year-old female. The radical nephrectomy was performed. The tumour was a well- circumscribed, solid mass attached to the renal pelvis without necrosis and haemorrhage. Histopathologically, a spindle cell neoplasia with alternating hypo and hypercellular areas, storiform, fascicular and hemangipericytoma- like growth pattern and less cellular dense collagen deposits were observed. Immunohistochemical studies revealed reactivity for CD34, CD99 and Bcl-2 protein.
dc.identifier.doihttps://doi.org/10.31729/jnma.485
dc.identifier.urihttps://hdl.handle.net/20.500.14572/8220
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.titleRare solitary fibrous tumour of kidney
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage390
oaire.citation.startPage388
relation.isJournalIssueOfPublication22c338ba-3239-42cd-b94b-32397e5e8b5a
relation.isJournalIssueOfPublication.latestForDiscovery22c338ba-3239-42cd-b94b-32397e5e8b5a
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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