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ISSN: 1233-9687
Polish Journal of Pathology
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4/2013
vol. 64
 
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abstract:

Bilateral papillary renal cell carcinoma and angiomyolipoma in the patients with autosomal dominant polycystic kidney disease: case 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

POL J PATHOL 2013; 64 (4): 303-307
DOI: https://doi.org/10.5114/pjp.2013.39340
Online publish date: 2013/12/26
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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.
keywords:

autosomal dominant polycystic kidney disease, papillary renal cell carcinoma, angiomyolipoma
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