@Article{Konosu-Fukaya2013,
journal="Polish Journal of Pathology",
issn="1233-9687",
volume="64",
number="4",
year="2013",
title="Bilateral papillary renal cell carcinoma and angiomyolipoma in the patients with autosomal dominant polycystic kidney disease: case report of two cases and literature review",
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.",
author="Konosu-Fukaya, Sachiko
and Nakamura, Yasuhiro
and Fujishima, Fumiyoshi
and Kasajima, Atsuko
and Takahashi, Yayoi
and Joh, Kensuke
and Ikeda, Yoshihiro
and Ioritani, Naomasa
and Watanabe, Mika
and Sasano, Hironobu",
pages="303--307",
doi="10.5114/pjp.2013.39340",
url="http://dx.doi.org/10.5114/pjp.2013.39340"
}