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Journal of Korean Medical Science ; : 284-286, 2003.
Article in English | WPRIM | ID: wpr-210098

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.


Subject(s)
Aged , Female , Humans , Male , Abdomen/pathology , Kidney/abnormalities , Pedigree , Polycystic Kidney, Autosomal Dominant/diagnosis , Polycystic Kidney, Autosomal Dominant/pathology , Polycystic Kidney, Autosomal Dominant/physiopathology , Radiopharmaceuticals/metabolism , Technetium Tc 99m Dimercaptosuccinic Acid/metabolism
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