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

Authors :
Jeong GH
Park BS
Jeong TK
Ma SK
Yeum CH
Kim SW
Kim NH
Choi KC
Source :
Journal of Korean medical science [J Korean Med Sci] 2003 Apr; Vol. 18 (2), pp. 284-6.
Publication Year :
2003

Abstract

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 endstage 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.

Details

Language :
English
ISSN :
1011-8934
Volume :
18
Issue :
2
Database :
MEDLINE
Journal :
Journal of Korean medical science
Publication Type :
Academic Journal
Accession number :
12692431
Full Text :
https://doi.org/10.3346/jkms.2003.18.2.284