| Literature DB >> 21267700 |
Naoto Kuroda1, Tomoyuki Shiotsu, Ondrej Hes, Michal Michal, Taro Shuin, Gang-Hong Lee.
Abstract
Acquired cystic disease (ACD)-associated renal cell carcinoma (RCC) has been recently described. To date, there are no reports on genetic findings of G-band karyotype of ACD-associated RCC. In this article, we report the first report of G-band karyotype of ACD-associated RCC. A 66-year-old Japanese man was found to have a left renal tumor during the follow-up of hemodialysis consequent to chronic renal failure. Left nephrectomy was performed. Histological examination of three tumors in the left kidney showed the cribriform or microcystic growth pattern of neoplastic cells with eosinophilic cytoplasm, and many oxalate crystals were observed. The G-band karyotype of ACD-associated RCC showed 49, X, +X, -Y, +3, +7, +16. These chromosomal abnormalities resemble those of sporadic papillary RCC that has been previously reported. Finally, we suggest that this tumor may show a close relationship between ACD-associated RCC and papillary RCC, but a large-scale study will be needed to clarify the relationship between ACD-associated RCC and papillary RCC.Entities:
Mesh:
Year: 2011 PMID: 21267700 DOI: 10.1007/s00795-009-0465-8
Source DB: PubMed Journal: Med Mol Morphol ISSN: 1860-1499 Impact factor: 2.309