Bilateral papillary renal cell carcinoma and angiomyolipoma in the patients with autosomal dominant polycystic kidney disease: case report of two cases and literature review.

نویسندگان

  • S Konosu-Fukaya
  • Y Nakamura
  • F Fujishima
  • A Kasajima
  • Y Takahashi
  • K Joh
  • Y Ikeda
  • N Ioritani
  • M Watanabe
  • H Sasano
چکیده

We herein report two rare cases of bilateral renal neoplasms associated with autosomal dominant polycystic kidney disease (ADPKD). Case 1: Bilateral nephrectomy was performed on bilateral renal masses in a 58-year-old man with ADPKD. Case 2: Bilateral nephrectomy was performed on bilateral renal masses in a 32-year-old man with clinically suspected ADPKD. In case 1, angiomyolipoma (AML) and papillary renal cell carcinoma (PRCC) (type 1) were detected in the bilateral kidneys. In case 2, PRCC (type 1) was detected in the bilateral kidneys.

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عنوان ژورنال:
  • Polish journal of pathology : official journal of the Polish Society of Pathologists

دوره 64 4  شماره 

صفحات  -

تاریخ انتشار 2013