Unilateral autosomal dominant polycystic kidney disease with contralateral renal agenesis: A case report

被引：8
|
作者：
Jeong, GH
Park, BS
Jeong, TK
Ma, SK
Yeum, CH
Kim, SW
Kim, NH
Choi, KC
机构：
[1] Chonnam Natl Univ, Dept Internal Med, Sch Med, Gwangju 501757, South Korea
[2] Cheju Natl Univ Med Sch, Jeju, South Korea
来源：
JOURNAL OF KOREAN MEDICAL SCIENCE | 2003年 / 18卷 / 02期
关键词：
polycystic kidney; autosomal dominant; organogenesis; renal dialysis;
D O I：
10.3346/jkms.2003.18.2.284
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary renal disease. There are some reports in the literature concerning unilateral ADPKD. However, in adults, only a few cases of unilateral ADPKD with agenesis of contralateral kidney have been reported. We present a case of unilateral ADPKD with agenesis of contralateral kidney in a 66-yr-old man. Radiographic images showed the enlarged right kidney with multiple variable-sized cysts and the absence of the left kidney. The diagnosis of ADPKD was confirmed by the family screening. The patient received maintenance hemodialysis for end-stage renal disease. We report a case of unilateral ADPKD associated with contralateral renal agenesis in a 66-yr-old male patient with a literature review.
引用
收藏
页码：284 / 286
页数：3
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