pubmed-article:14571432 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:14571432 | lifeskim:mentions | umls-concept:C1266042 | lld:lifeskim |
pubmed-article:14571432 | lifeskim:mentions | umls-concept:C1510411 | lld:lifeskim |
pubmed-article:14571432 | pubmed:issue | 5 | lld:pubmed |
pubmed-article:14571432 | pubmed:dateCreated | 2003-10-22 | lld:pubmed |
pubmed-article:14571432 | pubmed:abstractText | We 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:14571432 | pubmed:language | eng | lld:pubmed |
pubmed-article:14571432 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14571432 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:14571432 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:14571432 | pubmed:month | Oct | lld:pubmed |
pubmed-article:14571432 | pubmed:issn | 1092-9134 | lld:pubmed |
pubmed-article:14571432 | pubmed:author | pubmed-author:AyalaAlberto... | lld:pubmed |
pubmed-article:14571432 | pubmed:author | pubmed-author:AbrahamsNeil... | lld:pubmed |
pubmed-article:14571432 | pubmed:author | pubmed-author:CzerniakBogda... | lld:pubmed |
pubmed-article:14571432 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:14571432 | pubmed:volume | 7 | lld:pubmed |
pubmed-article:14571432 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:14571432 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:14571432 | pubmed:pagination | 296-9 | lld:pubmed |
pubmed-article:14571432 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
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pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:meshHeading | pubmed-meshheading:14571432... | lld:pubmed |
pubmed-article:14571432 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:14571432 | pubmed:articleTitle | Chromophobe renal cell carcinoma with sarcomatoid transformation. | lld:pubmed |
pubmed-article:14571432 | pubmed:affiliation | Department of Pathology, The University of Texas, MD Anderson Cancer Center, Houston, TX 77030, USA. | lld:pubmed |
pubmed-article:14571432 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:14571432 | pubmed:publicationType | Case Reports | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:14571432 | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:14571432 | lld:pubmed |