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

研究成果: Article査読

8 被引用数 (Scopus)

抄録

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.

本文言語English
ページ(範囲)303-307
ページ数5
ジャーナルPolish Journal of Pathology
64
4
DOI
出版ステータスPublished - 2013

ASJC Scopus subject areas

  • 病理学および法医学

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