Y. Enoki, G. Katoh, H. Okabe and A. Yanagisawa, “Clinicopathological Features and CD57 Expression in Renal Cell Carcinoma in Acquired Cystic Disease of the Kidneys: With Special Emphasis on a Relation to the Duration of Haemodialysis, the Degree of Calcium Oxalate Deposition, Histological Type, and Possible Tumorigenesis,” Histopathology, Vol. 56, No. 3, pp. 384- 394. doi:10.1111/j.1365-2559.2010.03480.x

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.