Literature DB >> 17352162

[Bilateral renal cell carcinoma associated with polycystic kidney disease: case report and literature review].

Taku Kato1, Yoshito Takahashi, Keita Nakane, Shigeaki Yokoi, Hidetoshi Ehara, Ikuo Shinoda, Takashi Deguchi.   

Abstract

A 56-year-old Japanese man consulted a urologist because of urethral bleeding. He had been undergoing hemodialysis for the past 15 years due to polycystic kidney disease. Computed tomography revealed an irregular cyst wall in the left kidney. Since a neoplasm could not be ruled out, we removed the left kidney, by laparoscopic radical nephrectomy after obtaining the patient's consent. Histopathologic diagnosis was renal cell carcinoma. Fourteen months after the operation, urethral bleeding recurred. Further examination of the bladder and the urethra revealed no significant abnormalities. The patient insisted on right nephrectomy. Therefore, laparoscopic radical nephrectomy was performed. Histopathologic diagnosis was also renal cell carcinoma. Renal cell carcinoma in patients with end-stage renal disease is fairly common and is associated with acquired cystic kidney disease. However, renal cell carcinoma associated with polycystic kidney disease is extremely rare.

Entities:  

Mesh:

Year:  2007        PMID: 17352162

Source DB:  PubMed          Journal:  Hinyokika Kiyo        ISSN: 0018-1994


  2 in total

1.  Sarcomatoid renal cell carcinoma with autosomal dominant polycystic kidney disease: a case report and literature review.

Authors:  Yuji Hakozaki; Kiyotaka Uchiyama; Akane Yanai; Daisuke Yamada; Yuka Kamijo; Yoshitaka Ishibashi
Journal:  CEN Case Rep       Date:  2020-10-16

2.  Multifocal renal cell carcinoma of different histological subtypes in autosomal dominant polycystic kidney disease.

Authors:  Ki Yong Na; Hyun-Soo Kim; Yong-Koo Park; Sung-Goo Chang; Youn Wha Kim
Journal:  Korean J Pathol       Date:  2012-08-23
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.