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Japanese

A CASE OF CONGENITAL UNILATERAL MULTICYSTIC KIDNEY Shigeru Kakimoto 1 , Toru Tasaki 1 , Naofumi Matsunaga 2 , Yuhei Amamoto 2 , Mizuko Itoh 3 , Koh Imamura 3 , Ichiro Sekine 4 , Rhysaburo Takao 5 1Division of Urology, Nagasaki Chuo National Hospital pp.871-874
Published Date 1980/9/20
DOI https://doi.org/10.11477/mf.1413203017
  • Abstract
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Congenital unilateral multicystic kidney has been so far considered as a relatively rare disease with only cases reported in Japanese literature during the period of 1961 through 1975 by Sakai et al. Now-adays, however, this disease is no longer considered rare although if it is difficult to diagnose this lesion prior to surgical treatment. Our case, a four-month-old girl, could be diagnosed as having this disease before surgical treatment by means of computed tomography and renal scintigram. It is felt that com-puted tomography is a very useful technique for diagnosing the renal cystic disease.


Copyright © 1980, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1332 印刷版ISSN 0385-2393 医学書院

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