Rare Tumors (Nov 2013)

Bilateral tubulocystic renal cell carcinomas in diabetic end-stage renal disease: first case report with cytogenetic and ultrastructural studies

  • Max Xiangtian Kong,
  • Christopher Hale,
  • Antonio Subietas-Mayol,
  • Peng Lee,
  • Nicholas D. Cassai,
  • Gerald McRae,
  • David S. Goldfarb,
  • Ming Zhou,
  • Rosemary Wieczorek

DOI
https://doi.org/10.4081/rt.2013.e57
Journal volume & issue
Vol. 5, no. 4
pp. e57 – e57

Abstract

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Tubulocystic renal cell carcinoma (TC-RCC) is a rare renal tumor composed of well-differentiated tubules and cysts lined by neoplastic cells with eosinophilic cytoplasm and prominent nucleoli. The origin of the tumor cells is still controversial. TC-RCC typically arises unilaterally. Involvement of both kidneys by multifocal TC-RCC has not been reported. In this study we report the first case of bilateral and multifocal TC-RCC. Immunohistochemical, cytogenetic and ultrastructural studies suggest TC-RCC is closely related to papillary RCC.

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