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

Sachiko Konosu-Fukaya, Yasuhiro Nakamura, Fumiyoshi Fujishima, Atsuko Kasajima, Yayoi Takahashi, Kensuke Joh, Yoshihiro Ikeda, Naomasa Ioritani, Mika Watanabe, Hironobu Sasano

Research output: Contribution to journalArticlepeer-review

8 Citations (Scopus)

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 renalmasses in a 58-year-oldman 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.

Original languageEnglish
Pages (from-to)303-307
Number of pages5
JournalPolish Journal of Pathology
Volume64
Issue number4
DOIs
Publication statusPublished - 2013

Keywords

  • Angiomyolipoma
  • Autosomal dominant polycystic kidney disease
  • Papillary renal cell carcinoma

ASJC Scopus subject areas

  • Pathology and Forensic Medicine

Fingerprint Dive into the research topics of 'Bilateral papillary renal cell carcinoma and angiomyolipoma in patients with autosomal dominant polycystic kidney disease: Report of two cases and literature review'. Together they form a unique fingerprint.

Cite this