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S. K. Tickoo, M. N. DePeralta-Venturina, L. R. Harik, H. D. Worcester, M. E. Salama, A. N. Young, H. Moch and M. B. Amin, “Spectrum of Epithelial Neoplasms in End-Stage Renal Disease: An Experience from 66 Tumor-Bearing Kidneys with Emphasis on Histologic Patterns Distinct from Those in Sporadic Adult Renal Neoplasia,” American Journal of Surgical Pathology, Vol. 30, No. 2, 2006, pp. 141-153. doi:10.1097/01.pas.0000185382.80844.b1

has been cited by the following article:

• TITLE: Gain of Chromosomes 1, 2, 7, 10, 13 and 17 in an Acquired Cystic Kidney Disease Associated Renal Cell Carcinoma

  AUTHORS: Shuting Bai, Dengfeng Cao, Diane Robirds, Julie Branson, Zhanyong Bing

  KEYWORDS: ACDK-RCC; Oxalate; Interphase in Situ Hybridization

  JOURNAL NAME: Open Journal of Pathology, Vol.2 No.1, January 12, 2012

  ABSTRACT: The acquired cystic disease of the kidney-associated renal cell carcinoma (ACDK-RCC) in the current study occurred in a kidney with multiple cysts and was composed of cells with eosinophilic cytoplasm and prominent nucleoli. There were extensive calcium oxalate deposits in both non-neoplastic cysts and tumor. The tumor cells were positive for RCC Ma, CD10, and EMA, focally positive for CK7, negative for vimentin. Interphase in situ hybridizations (FISH) were performed for chromosome 1, 2, 7, 10, 13 and 17. No chromosomal abnormality was observed in the non-neoplastic cysts. Polysomies of chromosomes 1, 2, 7, 10, 13, 17 were observed in the tumor. Trisomy 13 was first reported in this type of tumor, which warranted further study.