Unilateral renal cystic disease in adults

被引：33
|
作者：
Hwang, DY
Ahn, C
Lee, JG
Kim, SH
Oh, HY
Kim, YY
Lee, ES
Han, JS
Kim, S
Lee, JS
机构：
[1] Seoul Natl Univ Hosp, Coll Med, Div Nephrol, Seoul 110744, South Korea
[2] Seoul Natl Univ Hosp, Coll Med, Div Radiol, Seoul 110744, South Korea
[3] Seoul Natl Univ Hosp, Coll Med, Div Urol, Seoul 110744, South Korea
[4] Sungkyunkwan Univ, Coll Med, Div Nephrol, Seoul, South Korea
来源：
NEPHROLOGY DIALYSIS TRANSPLANTATION | 1999年 / 14卷 / 08期
关键词：
autosomal dominant polycystic kidney disease; unilateral renal cystic disease;
D O I：
10.1093/ndt/14.8.1999
中图分类号：
R3 [基础医学]; R4 [临床医学];
学科分类号：
1001 ; 1002 ; 100602 ;
摘要：
Unilateral renal cystic disease (URCD) is morphologically indistinguishable from autosomal dominant polycystic kidney disease (ADPKD) except for its unilaterality. Unlike ADPKD, URCD patients show neither a genetic background nor progressive deterioration in renal function; thus, the differential diagnosis of URCD from ADPKD is important. Only a few cases of URCD have been reported. This study reports two cases of URCD in adults together with a literature review. We identified these two cases using abdominal computerized tomography;and family screening with renal ultrasonography.
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页码：1999 / 2003
页数：5
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