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

Pol J Pathol. 2013 Dec;64(4):303-7. doi: 10.5114/pjp.2013.39340.

Abstract

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.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Adult
  • Angiomyolipoma / complications
  • Angiomyolipoma / pathology*
  • Angiomyolipoma / surgery
  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Renal Cell / complications
  • Carcinoma, Renal Cell / pathology*
  • Carcinoma, Renal Cell / surgery
  • Humans
  • Kidney / pathology
  • Kidney / surgery
  • Kidney Neoplasms / complications
  • Kidney Neoplasms / pathology*
  • Kidney Neoplasms / surgery
  • Male
  • Middle Aged
  • Nephrectomy
  • Polycystic Kidney, Autosomal Dominant / complications
  • Polycystic Kidney, Autosomal Dominant / pathology*
  • Polycystic Kidney, Autosomal Dominant / surgery
  • Treatment Outcome

Substances

  • Biomarkers, Tumor

Supplementary concepts

  • Papillary renal cell carcinoma, sporadic