POLYCYSTIC KIDNEY OF AUTOSOMAL DOMINANT INHERITANCE, POLYCYSTIC LIVER AND CONGENITAL HEPATIC-FIBROSIS IN A SINGLE KINDRED

被引：16
作者：
MATSUDA, O
IDEURA, T
SHINODA, T
SHIIGAI, T
TAKEUCHI, H
CHEN, WC
MIYAKE, S
机构：
[1] MUSASHINO RED CROSS HOSP,DEPT PATHOL,MUSASHINO,TOKYO 180,JAPAN
[2] SHOWA UNIV,FUJIGAOKA HOSP,DEPT INTERNAL MED,YOKOHAMA,JAPAN
[3] SHINSHU UNIV,SCH MED,DEPT GERIATR,MATSUMOTO,NAGANO 390,JAPAN
[4] TORIDE KYODO HOSP,DEPT INTERNAL MED,TORIDE,IBARAKI,JAPAN
[5] MISHIMA HOSP,DEPT UROL,MISHIMA,SHIZUOKA,JAPAN
来源：
AMERICAN JOURNAL OF NEPHROLOGY | 1990年 / 10卷 / 03期
关键词：
Autosomal dominant polycystic kidney disease; Cerebral aneurysm; Congenital hepatic fibrosis; Polycystic kidney; Polycystic liver;
D O I：
10.1159/000168088
中图分类号：
R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];
学科分类号：
1002 ; 100201 ;
摘要：
A family with clear evidence of concominant congenital hepatic fibrosis, polycystic liver and adult-type polycystic kidney is reported. The autosomal dominant inheritance of polycystic kidney in association with either liver cyst or hepatic fibrosis in this family suggests that various combinations of hepatic and renal fibrocystic lesions are possible to occur. Additionally, in the proband a very rare association of congenital hepatic fibrosis and cerebral aneurysm was present. © 1990 S. Karger AG, Basel.
引用
收藏
页码：237 / 241
页数：5
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