Publication:
Solitary fibrous tumor of the kidney

dc.contributor.authorKAYA, HANDAN
dc.contributor.authorBOZKURT, SÜHEYLA
dc.contributor.authorsBozkurt, Suheyla Uyar; Ahiskali, Rengin; Kaya, Handan; Demir, Aslan; Ilker, Yalcin
dc.date.accessioned2022-03-12T17:32:32Z
dc.date.accessioned2026-01-11T13:15:32Z
dc.date.available2022-03-12T17:32:32Z
dc.date.issued2007
dc.description.abstractSolitary fibrous tumors are rare spindle cell neoplasms usually arising in the pleura. They have, however, also been reported at extrapleural locations. Solitary fibrous tumor (SFT) of the kidney is rare. Despite its rarity, histological diagnosis of solitary fibrous tumor is crucial to avoid misdiagnosis with other more aggressive tumors arising in the kidney. We report a solitary fibrous tumor of the left kidney that presented as a malignant tumor in a 51-year-old woman, and include clinical and radiographic findings. The tumor was well circumscribed and composed of spindle cells in a collagenous stroma. Immunohistochemistry showed reactivity for vimentin, CD 34, BCL-2 protein and CD99. Immunohistochemical stains for cytokeratin, S-100, desmin, alpha-smooth muscle actin and HMB-45 were negative. A diagnosis of SFT was made based on light microscopy and immunohistochemistry.
dc.identifier.doi10.1111/j.1600-0463.2007.apm_500.x
dc.identifier.eissn1600-0463
dc.identifier.issn0903-4641
dc.identifier.pubmed17367473
dc.identifier.urihttps://hdl.handle.net/11424/228611
dc.identifier.wosWOS:000244881000012
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofAPMIS
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectsolitary fibrous tumor
dc.subjectCD 34
dc.subjectBCL-2
dc.subjectCD99
dc.subjectkidney
dc.subjectSPECTRUM
dc.subjectBENIGN
dc.titleSolitary fibrous tumor of the kidney
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage262
oaire.citation.issue3
oaire.citation.startPage259
oaire.citation.titleAPMIS
oaire.citation.volume115

Files