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Unilateral Autosomal Dominant Polycystic Kidney Disease with Contralateral Renal Agenesis: A Case Report
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / Polycystic Kidney, Autosomal Dominant / Radiopharmaceuticals / Technetium Tc 99m Dimercaptosuccinic Acid / Abdomen / Kidney Limits: Aged / Female / Humans / Male Language: English Journal: Journal of Korean Medical Science Year: 2003 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pedigree / Polycystic Kidney, Autosomal Dominant / Radiopharmaceuticals / Technetium Tc 99m Dimercaptosuccinic Acid / Abdomen / Kidney Limits: Aged / Female / Humans / Male Language: English Journal: Journal of Korean Medical Science Year: 2003 Type: Article