Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:14571432rdf:typepubmed:Citationlld:pubmed
pubmed-article:14571432lifeskim:mentionsumls-concept:C1266042lld:lifeskim
pubmed-article:14571432lifeskim:mentionsumls-concept:C1510411lld:lifeskim
pubmed-article:14571432pubmed:issue5lld:pubmed
pubmed-article:14571432pubmed:dateCreated2003-10-22lld:pubmed
pubmed-article:14571432pubmed:abstractTextWe present a rare case of a chromophobe renal cell carcinoma that progressed to a high-grade spindle cell sarcoma. The tumor affected a 50-year-old man who had presented with right upper quadrant discomfort and hematuria and subsequently underwent a right radical nephrectomy. Microscopically, the tumor was composed of two distinct components, a chromophobe renal cell carcinoma and a sarcomatoid component. The sarcomatoid component had exhibited aggressive behavior by spreading to a regional lymph node. This case report shows that chromophobe carcinoma can develop a sarcomatoid transformation with a high propensity for invasive growth and metastasis.lld:pubmed
pubmed-article:14571432pubmed:languageenglld:pubmed
pubmed-article:14571432pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:14571432pubmed:citationSubsetIMlld:pubmed
pubmed-article:14571432pubmed:statusMEDLINElld:pubmed
pubmed-article:14571432pubmed:monthOctlld:pubmed
pubmed-article:14571432pubmed:issn1092-9134lld:pubmed
pubmed-article:14571432pubmed:authorpubmed-author:AyalaAlberto...lld:pubmed
pubmed-article:14571432pubmed:authorpubmed-author:AbrahamsNeil...lld:pubmed
pubmed-article:14571432pubmed:authorpubmed-author:CzerniakBogda...lld:pubmed
pubmed-article:14571432pubmed:issnTypePrintlld:pubmed
pubmed-article:14571432pubmed:volume7lld:pubmed
pubmed-article:14571432pubmed:ownerNLMlld:pubmed
pubmed-article:14571432pubmed:authorsCompleteYlld:pubmed
pubmed-article:14571432pubmed:pagination296-9lld:pubmed
pubmed-article:14571432pubmed:dateRevised2004-11-17lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:meshHeadingpubmed-meshheading:14571432...lld:pubmed
pubmed-article:14571432pubmed:year2003lld:pubmed
pubmed-article:14571432pubmed:articleTitleChromophobe renal cell carcinoma with sarcomatoid transformation.lld:pubmed
pubmed-article:14571432pubmed:affiliationDepartment of Pathology, The University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA.lld:pubmed
pubmed-article:14571432pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:14571432pubmed:publicationTypeCase Reportslld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14571432lld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:14571432lld:pubmed