Z. Bing and J. Tomaszewski, “Clear Cell Papillary Renal Cell Carcinoma in the Bilateral Native Kidneys after 2 Years of Renal Transplantation: Report of a Case and Review of the Literature,” Case Reports in Transplantation, Vol. 2011, 2011, Article ID 387645, 4 pages. doi:10.1155/2011/387645

has been cited by the following article:

• TITLE: Clear Cell Papillary Renal Cell Carcinoma: A Rare Subtype

  AUTHORS: Armin Kamyab, Michael J. Jacobs

  KEYWORDS: Renal Cell Carcinoma, Clear Cell, Papillary

  JOURNAL NAME: Journal of Cancer Therapy, Vol.2 No.5, December 31, 2011

  ABSTRACT: Introduction: Renal cell carcinoma (RCC) is generally divided into clear cell, papillary, and chromophobe subtypes. Clear cell papillary RCC is a recently described subtype. Case report: We report the case of a 42 year old female who was found on computed tomography scan of the abdomen to have a cyst which appeared to involve the right kidney. Pathology of the cyst wall revealed features consistent with a RCC, clear cell papillary type. Discussion: Clear cell papillary RCC are a recently described entity with less than 100 cases reported in the literature. Most cases in the literature have been associated with end-stage renal disease, however more case are being reported in patients without renal disease. Conclusion: Clear cell papillary RCC is a rare distinct entity in the spectrum of renal cell carcinoma. Based on the literature they appear to be clinically indolent tumors; however, more research is required to further characterize and prognosticate these rare tumors.