Polish Journal of Pathology

Abstract

4/2013 vol. 64

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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Confronting perimenopausal women’s knowledge of coronary heart disease with their health behaviours. Controversial role of hormone replacement therapy in the protection of coronary heart disease
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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