Bilateral congenital multicystic dysplasia of the kidney

Teruaki Kishikawa; Takashi Toda; Hiroshi Ito; Shigeru Yamaguchi; Makoto Kuroda; Koji Matsuyama

doi:10.1007/BF02468838

Bilateral congenital multicystic dysplasia of the kidney

Teruaki Kishikawa
, Takashi Toda
, Hiroshi Ito
, Shigeru Yamaguchi
, Makoto Kuroda
, Koji Matsuyama

医学部・病理診断学

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

3 被引用数 (Scopus)

抄録

The clinical and pathological features of congenital multicystic dysplasia of the kidney are reviewed and we report of a patient with bilateral dysplasia who lived longer than do most such patients. When multicystic disease of the kidney is bilateral, it is commonly confused with polycystic disease. Despite the fatal prognosis, differentiation is essential for appropriate genetic counselling since multicystic disease is not a familial occurrence.

本文言語	英語
ページ（範囲）	198-202
ページ数	5
ジャーナル	Japanese Journal of Surgery
巻	11
号	3
DOI	https://doi.org/10.1007/BF02468838
出版ステータス	出版済み - 05-1981

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外科

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10.1007/BF02468838

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title = "Bilateral congenital multicystic dysplasia of the kidney",

abstract = "The clinical and pathological features of congenital multicystic dysplasia of the kidney are reviewed and we report of a patient with bilateral dysplasia who lived longer than do most such patients. When multicystic disease of the kidney is bilateral, it is commonly confused with polycystic disease. Despite the fatal prognosis, differentiation is essential for appropriate genetic counselling since multicystic disease is not a familial occurrence.",

author = "Teruaki Kishikawa and Takashi Toda and Hiroshi Ito and Shigeru Yamaguchi and Makoto Kuroda and Koji Matsuyama",

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AU - Kishikawa, Teruaki

AU - Toda, Takashi

AU - Ito, Hiroshi

AU - Yamaguchi, Shigeru

AU - Kuroda, Makoto

AU - Matsuyama, Koji

PY - 1981/5

Y1 - 1981/5

N2 - The clinical and pathological features of congenital multicystic dysplasia of the kidney are reviewed and we report of a patient with bilateral dysplasia who lived longer than do most such patients. When multicystic disease of the kidney is bilateral, it is commonly confused with polycystic disease. Despite the fatal prognosis, differentiation is essential for appropriate genetic counselling since multicystic disease is not a familial occurrence.

AB - The clinical and pathological features of congenital multicystic dysplasia of the kidney are reviewed and we report of a patient with bilateral dysplasia who lived longer than do most such patients. When multicystic disease of the kidney is bilateral, it is commonly confused with polycystic disease. Despite the fatal prognosis, differentiation is essential for appropriate genetic counselling since multicystic disease is not a familial occurrence.

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DO - 10.1007/BF02468838

M3 - Article

C2 - 7277897

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JO - Japanese Journal of Surgery

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Bilateral congenital multicystic dysplasia of the kidney

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